نتایج جستجو برای: genetic modifiers

تعداد نتایج: 620378  

Journal: :The Journal of Experimental Medicine 2002
Silvia Bolland Young-Sun Yim Katalin Tus Edward K. Wakeland Jeffrey V. Ravetch

FcgammaRIIB is a potent lupus susceptibility gene as demonstrated by the observation that mice deficient in this molecule develop spontaneous antinuclear antibodies (ANA) and fatal glomerulonephritis when on the C57BL/6 background. To determine the mechanisms underlying the epistasis displayed by this gene we have constructed hybrids between FcgammaRIIB(-/-) and the systemic lupus erythematosus...

Journal: :Cardiovascular research 2012
Jason R Becker Tamara Y Robinson Chetana Sachidanandan Amy E Kelly Shannon Coy Randall T Peterson Calum A MacRae

AIMS Despite increased understanding of the fundamental biology regulating cardiomyocyte hypertrophy and heart failure, it has been challenging to find novel chemical or genetic modifiers of these pathways. Traditional cell-based methods do not model the complexity of an intact cardiovascular system and mammalian models are not readily adaptable to chemical or genetic screens. Our objective was...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
A R Shoemaker A R Moser C A Midgley L Clipson M A Newton W F Dove

Previous studies of Min/+ (multiple intestinal neoplasia) mice on a sensitive genetic background, C57BL/6 (B6), showed that adenomas have lost heterozygosity for the germ-line ApcMin mutation in the Apc (adenomatous polyposis coli) gene. We now report that on a strongly resistant genetic background, AKR/J (AKR), Min-induced adenoma multiplicity is reduced by about two orders of magnitude compar...

2013
Sudarshan Chari Ian Dworkin

The phenotypic outcome of a mutation cannot be simply mapped onto the underlying DNA variant. Instead, the phenotype is a function of the allele, the genetic background in which it occurs and the environment where the mutational effects are expressed. While the influence of genetic background on the expressivity of individual mutations is recognized, its consequences on the interactions between...

Journal: :Genetics 2009
Anne-Marie J Cziko Cathal T McCann Iris C Howlett Scott A Barbee Rebecca P Duncan Rene Luedemann Daniela Zarnescu Konrad E Zinsmaier Roy R Parker Mani Ramaswami

Mechanisms of neuronal mRNA localization and translation are of considerable biological interest. Spatially regulated mRNA translation contributes to cell-fate decisions and axon guidance during development, as well as to long-term synaptic plasticity in adulthood. The Fragile-X Mental Retardation protein (FMRP/dFMR1) is one of the best-studied neuronal translational control molecules and here ...

Journal: :Science signaling 2012
Kris C Wood David J Konieczkowski Cory M Johannessen Jesse S Boehm Pablo Tamayo Olga B Botvinnik Jill P Mesirov William C Hahn David E Root Levi A Garraway David M Sabatini

Cell microarrays are a promising tool for performing large-scale functional genomic screening in mammalian cells at reasonable cost, but owing to technical limitations they have been restricted for use with a narrow range of cell lines and short-term assays. Here, we describe MicroSCALE (Microarrays of Spatially Confined Adhesive Lentiviral Features), a cell microarray-based platform that enabl...

2014
Jennifer S Yokoyama Daniel S Evans Giovanni Coppola Joel H Kramer Gregory J Tranah Kristine Yaffe

OBJECTIVE Identify genetic factors associated with cognitive maintenance in late life and assess their association with gray matter (GM) volume in brain networks affected in aging. METHODS We conducted a genome-wide association study of ∼2.4 M markers to identify modifiers of cognitive trajectories in Caucasian participants (N = 7,328) from two population-based cohorts of non-demented elderly...

Journal: :Genetics 1956
J B Spofford

ANY mutant stocks of Drosophila mass cultured in the laboratory for generaM tions become phenotypically almost indistinguishable from wild type. Upon outcrossing, the mutant reappears in the FZ with its pristine strength of expression. Presumably, genes reducing the degree of expression, or expressivity, of the major character of the mutant stock had appeared and accumulated through natural sel...

Journal: :JAMA 2009
Jaclyn R Bartlett Kenneth J Friedman Simon C Ling Rhonda G Pace Scott C Bell Billy Bourke Giuseppe Castaldo Carlo Castellani Marco Cipolli Carla Colombo John L Colombo Dominique Debray Adriana Fernandez Florence Lacaille Milan Macek Marion Rowland Francesco Salvatore Christopher J Taylor Claire Wainwright Michael Wilschanski Dana Zemková William B Hannah M James Phillips Mary Corey Julian Zielenski Ruslan Dorfman Yunfei Wang Fei Zou Lawrence M Silverman Mitchell L Drumm Fred A Wright Ethan M Lange Peter R Durie Michael R Knowles

CONTEXT A subset (approximately 3%-5%) of patients with cystic fibrosis (CF) develops severe liver disease with portal hypertension. OBJECTIVE To assess whether any of 9 polymorphisms in 5 candidate genes (alpha(1)-antitrypsin or alpha(1)-antiprotease [SERPINA1], angiotensin-converting enzyme [ACE], glutathione S-transferase [GSTP1], mannose-binding lectin 2 [MBL2], and transforming growth fa...

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