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Quantitative PCR-Based Detection Of Typical And Atypical Bacterial Strains In COPD Patients And Relationship To Culture

DS Garcha, SJ Thurston, ARC Patel… - American Journal of …, 2011 - Am Thoracic Soc
B42 COPD PATHOGENESIS: CELLULAR EXPRESSION AND PROTEIN RESPONSES
16/8:15 AM-4:30 PM / Area E, Hall B (Upper Level), Colorado Convention Center ... Quantitative
Pcr-Based Detection Of Typical And Atypical Bacterial Strains In COPD Patients And ...
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Atypical Presentation and Novel StAR Protein Gene Mutation in a 46, XY Female with Lipoid Congenital Adrenal Hyperplasia

O Lekarev, Y Morel… - Hormonal and Genetic Basis of …, 2011 - books.google.com
Chapter 29 Atypical Presentation and Novel StAR Protein Gene Mutation in a 46, XY Female
with Lipoid Congenital Adrenal Hyperplasia Oksana Lekarev, Yves Morel, and Maria I. New Introduction
Congenital lipoid adrenal hyperplasia is a severe disorder of adrenal and gonadal ...
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The WNKs: atypical protein kinases with pleiotropic actions

[HTML] from nih.govJA McCormick… - Physiological reviews, 2011 - Am Physiological Soc
WNKs are serine/threonine kinases that comprise a unique branch of the kinome. They are
so-named owing to the unusual placement of an essential catalytic lysine. WNKs have now been
identified in diverse organisms. In humans and other mammals, four genes encode ...
Cited by 3 - Related articles - All 3 versions

The Role of Transmembrane Domain 3 in the Actions of Orthosteric, Allosteric, and Atypical Agonists of the M4 Muscarinic Acetylcholine Receptor

K Leach, AE Davey, CC Felder, PM Sexton… - Molecular …, 2011 - ASPET
Despite the discovery of a diverse range of novel agonists and allosteric modulators of the M
4 muscarinic acetylcholine (ACh) receptor (mAChR), little is known about how such ligands activate
the receptor. We used site-directed mutagenesis of conserved residues in ...
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CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

A Abyzov, AE Urban, M Snyder… - Genome Research, 2011 - genome.cshlp.org
Copy number variation (CNV) in the genome is a complex phenomenon, and not completely
understood. We have developed a method, CNVnator, for CNV discovery and genotyping from
read-depth (RD) analysis of personal genome sequencing. Our method is based on ...
Cited by 6 - Related articles - All 7 versions

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