<?xml version='1.0' encoding='UTF-8'?><feed xmlns='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/'><id>tag:blogger.com,1999:blog-27288554</id><updated>2008-11-25T14:11:48.143-08:00</updated><title type='text'>Molecular Biology and Bioinformatics News</title><subtitle type='html'></subtitle><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/'/><link rel='next' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default?start-index=26&amp;max-results=25'/><link rel='http://schemas.google.com/g/2005#feed' type='application/atom+xml' href='http://biomol.net/en/news/atom.xml'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><generator version='7.00' uri='http://www.blogger.com'>Blogger</generator><openSearch:totalResults>57</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>25</openSearch:itemsPerPage><entry><id>tag:blogger.com,1999:blog-27288554.post-4587330036299154929</id><published>2008-11-25T14:05:00.000-08:00</published><updated>2008-11-25T14:11:48.160-08:00</updated><title type='text'>Interpreting the Human Genome- THE MIAMI 2009 WINTER SYMPOSIUM</title><summary type='text'>The human genome has hidden levels of regulatory complexity and variability that have begun to reveal themselves since the initial sequence became available in 2001. Today, with increasingly powerful sequencing and analysis technologies, we are not only beginning to appreciate the scale of variation in individual human genome sequences, but also gaining a greater understanding of how genome </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/4587330036299154929/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=4587330036299154929' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4587330036299154929'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4587330036299154929'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/11/interpreting-human-genome-miami-2009.html' title='Interpreting the Human Genome- THE MIAMI 2009 WINTER SYMPOSIUM'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-5466835670059180935</id><published>2008-11-24T03:44:00.000-08:00</published><updated>2008-11-24T03:48:17.751-08:00</updated><title type='text'>Sequencing the mammoth genome</title><summary type='text'>In 1994, two independent groups extracted DNA from several Pleistocene epoch mammoths and noted differences among individual specimens. Subsequently, DNA sequences have been published for a number of extinct species. However, such ancient DNA is often fragmented and damaged, and studies to date have typically focused on short mitochondrial sequences, never yielding more than a fraction of a per </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/5466835670059180935/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=5466835670059180935' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5466835670059180935'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5466835670059180935'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/11/sequencing-mammoth-genome.html' title='Sequencing the mammoth genome'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-3866771847407189506</id><published>2008-11-18T14:56:00.000-08:00</published><updated>2008-11-18T15:04:26.598-08:00</updated><title type='text'>Genes and Social Behavior</title><summary type='text'>What genes and regulatory sequences contribute to the organization and functioning of neural circuits and molecular pathways in the brain that support social behavior? How does social experience interact with information in the genome to modulate brain activity? Here, we address these questions by highlighting progress that has been made in identifying and understanding two key "vectors of </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/3866771847407189506/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=3866771847407189506' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/3866771847407189506'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/3866771847407189506'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/11/genes-and-social-behavior.html' title='Genes and Social Behavior'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-4135899660478206455</id><published>2008-09-01T03:55:00.000-07:00</published><updated>2008-09-01T03:56:44.048-07:00</updated><title type='text'>Nuclear Membrane Mechanics</title><summary type='text'>In the fission yeast Schizosaccharomyces pombe, the nucleus is tethered to the cytoskeleton by KASH domain-containing proteins in the outer nuclear membrane and SUN domain-containing proteins in the inner nuclear membrane. By exerting force on these SUN-KASH complexes, the cytoskeleton controls the position of the nucleus within the cell. Centromeric DNA inside the nucleus has been observed to </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/4135899660478206455/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=4135899660478206455' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4135899660478206455'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4135899660478206455'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/09/nuclear-membrane-mechanics.html' title='Nuclear Membrane Mechanics'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-6911690791777562376</id><published>2008-08-09T15:40:00.000-07:00</published><updated>2008-08-09T15:45:17.229-07:00</updated><title type='text'>Postdoctoral in Stem Cells and  Neurodevelopment</title><summary type='text'>A Postdoctoral position is available for research in the areas of STEM CELLS AND NEURODEVELOPMENT. The laboratory, headed by Dr. Alysson R. Muotri, make use of human ES and iPS cells, in combination with genetic, molecular, biochemical and computational
tools, to study early stages of brain development and the formation of neuronal networks.
Research currently focuses on two interconnected </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/6911690791777562376/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=6911690791777562376' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/6911690791777562376'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/6911690791777562376'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/08/postdoctoral-in-stem-cells-and.html' title='Postdoctoral in Stem Cells and  Neurodevelopment'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-5067463087543665205</id><published>2008-08-07T13:05:00.000-07:00</published><updated>2008-08-07T13:09:55.153-07:00</updated><title type='text'>Mitochondrial Dysfunction in Neurological Disease</title><summary type='text'>Mitochondria are responsible for maintaining the energy balance of the cell and are also responsible for triggering apoptosis (programmed cell death) in response to oxidative stress. This one-day mini-symposium aims to highlight recent advances in our understanding of how these organelles function in the nervous system, and how mitochondrial dysfunction contributes to neurological disease.

</summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/5067463087543665205/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=5067463087543665205' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5067463087543665205'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5067463087543665205'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/08/mitochondrial-dysfunction-in.html' title='Mitochondrial Dysfunction in Neurological Disease'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-6913948056051824221</id><published>2008-08-01T15:02:00.000-07:00</published><updated>2008-08-01T15:04:51.872-07:00</updated><title type='text'>Stem Cells and Amyotrophic Lateral Sclerosis</title><summary type='text'>The generation of pluripotent stem cells from an individual patient would enable the large-scale production of the cell-types affected by that patient’s disease. These cells could in turn be used for disease modeling, drug discovery, and eventually autologous cell-replacement therapies. Although recent studies have demonstrated the reprogramming of human fibroblasts to a pluripotent state, it </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/6913948056051824221/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=6913948056051824221' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/6913948056051824221'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/6913948056051824221'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/08/stem-cells-and-amyotrophic-lateral.html' title='Stem Cells and Amyotrophic Lateral Sclerosis'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-8199216158976959565</id><published>2008-03-19T05:18:00.000-07:00</published><updated>2008-03-19T05:22:55.022-07:00</updated><title type='text'>Yeast Prion Protein Structure Revealed</title><summary type='text'>Prion proteins are linked to several diseases, including bovine spongiform encephalopathy in cattle, scrapie in sheep, and Creutzfeldt-Jakob disease in humans. Infectious prion-like proteins that also form amyloid fibrils are found in yeast and other fungi. Based on solid-state nuclear magnetic resonance data, Wasmer et al. provide a structural model of amyloid fibrils from the prion-forming </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/8199216158976959565/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=8199216158976959565' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/8199216158976959565'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/8199216158976959565'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/03/yeast-prion-protein-structure-revealed.html' title='Yeast Prion Protein Structure Revealed'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-6331976638277533840</id><published>2008-03-11T07:19:00.000-07:00</published><updated>2008-03-11T07:40:55.337-07:00</updated><title type='text'>Mutations associated with Autism</title><summary type='text'>Although autism is highly heritable, sorting out the genes associated with this complex disease has been difficult. Weiss et al. searched for structural mutations (duplications or deletions below the level of microscopic detection) in the genomic DNA of 751 families who are part of the Autism Genetic Resource Exchange. They found a significant association of autism with a nearly 600-kb region </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/6331976638277533840/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=6331976638277533840' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/6331976638277533840'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/6331976638277533840'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/03/mutations-associated-with-autism.html' title='Mutations associated with Autism'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-4362657696397661861</id><published>2008-02-18T04:19:00.000-08:00</published><updated>2008-02-18T04:24:26.271-08:00</updated><title type='text'>International Congress of Genetics</title><summary type='text'>Genomics revolutionized genetic research. Now, complete annotated genome 
sequences are available for the human, our closest relative, the chimpanzee, 
and for many other model organisms. Multiple genomes have been compared and 
scrutinized for past and ongoing processes of variation, adaptation and speciation. Traces of the foregoing RNA world show it to be far more influential than previously </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/4362657696397661861/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=4362657696397661861' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4362657696397661861'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4362657696397661861'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/02/international-congress-of-genetics.html' title='International Congress of Genetics'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-8713094340758986738</id><published>2008-02-08T05:32:00.000-08:00</published><updated>2008-02-08T07:06:24.982-08:00</updated><title type='text'>GENOMICS A High-Salt Lifestyle</title><summary type='text'>Bonneau et al. describe progress in an effort to link systems-level analysis to events at the molecular and organismal levels. Using experiments and computation, they have pooled transcriptome, protein-protein interaction, structural, and evolution-related data to generate a dynamic model of the halophilic organism Halobacterium salinarum. This model was trained on data sets that included more </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/8713094340758986738/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=8713094340758986738' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/8713094340758986738'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/8713094340758986738'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/02/genomics-high-salt-lifestyle.html' title='GENOMICS A High-Salt Lifestyle'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-9222544036193822861</id><published>2008-02-02T05:10:00.000-08:00</published><updated>2008-02-02T05:15:18.519-08:00</updated><title type='text'>DNA-Assisted Molecular Delivery</title><summary type='text'>Many examples have been reported of assembly of atoms and small molecules into patterns on surfaces by pick up, transfer, and release with a scanning probe microscope tip under vacuum conditions. Kufer et al. assembled larger single molecules into patterns on surfaces in aqueous solution with an atomic force microscope (AFM) tip by taking advantage of differential forces acting on double-stranded</summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/9222544036193822861/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=9222544036193822861' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/9222544036193822861'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/9222544036193822861'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/02/dna-assisted-molecular-delivery.html' title='DNA-Assisted Molecular Delivery'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-2224724017965743194</id><published>2008-01-13T02:44:00.000-08:00</published><updated>2008-01-13T02:46:29.203-08:00</updated><title type='text'>Post-doc positions in bioinformatics</title><summary type='text'>The Computational Genomics Laboratory (www.evocell.org) is looking for
a post-doctoral fellow to work on the origins and evolution of
intracellular compartmentalization and protein trafficking pathways,
and a second post-doctoral fellow to work, in collaboration with the
Cell Cycle Regulation Lab (http://sites.igc.gulbenkian.pt/ccr/), in
the evolution of centrioles and their regulatory pathways. </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/2224724017965743194/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=2224724017965743194' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/2224724017965743194'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/2224724017965743194'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2008/01/post-doc-positions-in-bioinformatics.html' title='Post-doc positions in bioinformatics'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-5549375766501399175</id><published>2007-12-22T09:05:00.000-08:00</published><updated>2007-12-22T09:13:56.992-08:00</updated><title type='text'>Heavy breathing proteins</title><summary type='text'>Chronic obstructive pulmonary disease (COPD) is one of the most common adult respiratory diseases worldwide and the fourth leading cause of death. The American Lung Association estimates that about 15 million US citizens are affected. In the UK, the 30,000 deaths annually mean that more die of COPD than from breast, colon or prostate cancer. Despite the high prevalence, COPD is preventable and </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/5549375766501399175/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=5549375766501399175' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5549375766501399175'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5549375766501399175'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/12/heavy-breathing-proteins.html' title='Heavy breathing proteins'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-7086658410800615574</id><published>2007-09-05T05:39:00.000-07:00</published><updated>2007-09-05T06:05:27.567-07:00</updated><title type='text'>The Diploid Genome Sequence of an Individual Human</title><summary type='text'>Presented here is a genome sequence of an individual human. It was produced from ∼32 million random DNA fragments, sequenced by Sanger dideoxy technology and assembled into 4,528 scaffolds, comprising 2,810 million bases (Mb) of contiguous sequence with approximately 7.5-fold coverage for any given region. We developed a modified version of the Celera assembler to facilitate the identification </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/7086658410800615574/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=7086658410800615574' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/7086658410800615574'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/7086658410800615574'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/09/diploid-genome-sequence-of-individual.html' title='The Diploid Genome Sequence of an Individual Human'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-935737808933261391</id><published>2007-08-14T16:06:00.000-07:00</published><updated>2007-08-14T16:16:04.466-07:00</updated><title type='text'>Divergence of Transcription Factor Binding Sites Across Related Yeast Species</title><summary type='text'>Characterization of interspecies differences in gene regulation is crucial for understanding the molecular basis of both phenotypic diversity and evolution. By means of chromatin immunoprecipitation and DNA microarray analysis, the divergence in the binding sites of the pseudohyphal regulators Ste12 and Tec1 was determined in the yeasts Saccharomyces cerevisiae, S. mikatae, and S. bayanus under </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/935737808933261391/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=935737808933261391' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/935737808933261391'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/935737808933261391'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/08/divergence-of-transcription-factor.html' title='Divergence of Transcription Factor Binding Sites Across Related Yeast Species'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-1862123393932300770</id><published>2007-08-10T07:22:00.000-07:00</published><updated>2007-08-10T07:28:29.066-07:00</updated><title type='text'>AAV Vector Integration Sites in Mouse Hepatocellular Carcinoma</title><summary type='text'>Adeno-associated viruses (AAV) are promising gene therapy vectors that have little or no acute toxicity. We show that normal mice and mice with mucopolysaccharidosis VII (MPS VII) develop hepatocellular carcinoma (HCC) after neonatal injection of an AAV vector expressing b-glucuronidase. AAV proviruses were isolated from four tumors and were all located within a 6-kilobase region of chromosome 12</summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/1862123393932300770/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=1862123393932300770' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/1862123393932300770'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/1862123393932300770'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/08/aav-vector-integration-sites-in-mouse.html' title='AAV Vector Integration Sites in Mouse Hepatocellular Carcinoma'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-4728879458359356871</id><published>2007-07-16T07:18:00.000-07:00</published><updated>2007-07-16T07:25:59.981-07:00</updated><title type='text'>Growth Hormone and Development</title><summary type='text'>During development, genes are often transcribed in a temporally and spatially regulated manner. The murine growth hormone gene is differentially expressed in the developing pituitary gland. Lunyak et al. now examine the region surrounding the growth hormone gene and show that a repeated DNA sequence (short interspersed nuclear element B2) in the growth hormone locus functions as an insulator to </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/4728879458359356871/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=4728879458359356871' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4728879458359356871'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4728879458359356871'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/07/growth-hormone-and-development.html' title='Growth Hormone and Development'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-7152039392139510490</id><published>2007-07-01T07:07:00.000-07:00</published><updated>2007-07-01T07:11:23.083-07:00</updated><title type='text'>Genome Transplantation in Bacteria: Changing One Species to Another</title><summary type='text'>As a step toward propagation of synthetic genomes, we completely replaced the genome of a bacterial cell with one from another species by transplanting a whole genome as naked DNA. Intact genomic DNA from Mycoplasma mycoides large colony (LC), virtually free of protein, was transplanted into Mycoplasma capricolum cells by polyethylene glycol-mediated transformation. Cells selected for </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/7152039392139510490/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=7152039392139510490' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/7152039392139510490'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/7152039392139510490'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/07/genome-transplantation-in-bacteria.html' title='Genome Transplantation in Bacteria: Changing One Species to Another'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-2001803034848162118</id><published>2007-06-20T05:55:00.000-07:00</published><updated>2007-06-20T06:00:03.261-07:00</updated><title type='text'>Proteomic of  tarantula venom</title><summary type='text'>The venom itself is a cocktail of low- and high-molecular-weight components, the toxins constituting a very small proportion of these, often only one compound. They can be classified according to their mode of action and include neurotoxins (acting on the nervous system), cardiotoxins (heart), haemorrhagins (blood vessels), haemotoxins (blood), nephrotoxins (kidney), necrotoxins (tissue) and </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/2001803034848162118/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=2001803034848162118' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/2001803034848162118'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/2001803034848162118'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/06/proteomic-of-tarantula-venom.html' title='Proteomic of  tarantula venom'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-1681356875029864895</id><published>2007-06-15T07:09:00.000-07:00</published><updated>2007-06-15T07:12:18.359-07:00</updated><title type='text'>Noise in Gene Expression Determines Cell Fate in Bacillus subtilis</title><summary type='text'>Random cell-to-cell variations in gene expression within an isogenic population can lead to transitions between alternative states of gene expression. Little is known about how these variations (noise) in natural systems affects such transitions. In Bacillus subtilis, noise in ComK, the protein that regulates competence for DNA uptake, is thought to cause cells to transition to the competent </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/1681356875029864895/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=1681356875029864895' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/1681356875029864895'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/1681356875029864895'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/06/noise-in-gene-expression-determines.html' title='Noise in Gene Expression Determines Cell Fate in Bacillus subtilis'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-4720267532636923903</id><published>2007-05-06T06:12:00.000-07:00</published><updated>2007-05-06T06:16:32.441-07:00</updated><title type='text'>A Common Allele on Chromosome 9 Associated with Coronary Heart Disease</title><summary type='text'>Coronary heart disease (CHD) is a major cause of death in Western countries. Here we used genome-wide association scanning to identify a 58 kilobase interval on chromosome 9p21 that was consistently associated with CHD in six independent samples (n&gt; 23,000 participants) from four Caucasian populations. This interval, which is located near the CDKN2A and CDKN2B genes, contains no annotated genes </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/4720267532636923903/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=4720267532636923903' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4720267532636923903'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4720267532636923903'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/05/common-allele-on-chromosome-9.html' title='A Common Allele on Chromosome 9 Associated with Coronary Heart Disease'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-5093758236858744039</id><published>2007-04-15T16:56:00.000-07:00</published><updated>2007-04-15T17:17:00.624-07:00</updated><title type='text'>Rhesus Macaque Genome</title><summary type='text'>
The rhesus macaque (Macaca mulatta) is an abundant primate species that diverged from the ancestors of Homo sapiens about 25 million years ago. Because they are genetically and physiologically similar to humans, rhesus monkeys are the most widely used nonhuman primate in basic and applied biomedical research. We determined the genome sequence of an Indian-origin Macaca mulatta female and </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/5093758236858744039/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=5093758236858744039' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5093758236858744039'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/5093758236858744039'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/04/rhesus-macaque-genome.html' title='Rhesus Macaque Genome'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-4726561295363568908</id><published>2007-04-06T05:08:00.000-07:00</published><updated>2007-04-06T05:12:13.613-07:00</updated><title type='text'>Gene of small size in dogs</title><summary type='text'>
The domestic dog exhibits greater diversity in body size than any other terrestrial vertebrate. We used a strategy that exploits the breed structure of dogs to investigate the genetic basis of size. First, through a genome-wide scan, we identified a major quantitative trait locus (QTL) on chromosome 15 influencing size variation within a single breed. Second, we examined genetic variation in the</summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/4726561295363568908/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=4726561295363568908' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4726561295363568908'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/4726561295363568908'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/04/gene-of-small-size-in-dogs.html' title='Gene of small size in dogs'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-27288554.post-2810130426517319523</id><published>2007-03-31T16:21:00.000-07:00</published><updated>2007-03-31T16:23:48.517-07:00</updated><title type='text'>Key to Liver Regeneration</title><summary type='text'>The liver is one tissue in mammals that can regenerate. Passino et al. now find that hepatocyte proliferation is controlled by the neurotrophin receptor p75NTR, known primarily for its role in neurons in regulation of survival, apoptosis, and neuronal regeneration. Mice lacking p75NTR showed impaired hepatocyte proliferation. p75NTR appeared to act on hepatic stellate cells (HSCs), which </summary><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/2810130426517319523/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=27288554&amp;postID=2810130426517319523' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/2810130426517319523'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/27288554/posts/default/2810130426517319523'/><link rel='alternate' type='text/html' href='http://biomol.net/en/news/2007/03/key-to-liver-regeneration.html' title='Key to Liver Regeneration'/><author><name>BioMol.Net</name><email>noreply@blogger.com</email></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry></feed>