نتایج جستجو برای: missense

تعداد نتایج: 12396  

Journal: :The Prostate 2014
Anna M Johnson Kimberly A Zuhlke Chris Plotts Shannon K McDonnell Sumit Middha Shaun M Riska Daniel J Schaid Stephen N Thibodeau Julie A Douglas Kathleen A Cooney

BACKGROUND Family history is a major risk factor for prostate cancer (PCa), suggesting a genetic component to the disease. However, traditional linkage and association studies have failed to fully elucidate the underlying genetic basis of familial PCa. METHODS Here, we use a candidate gene approach to identify potential PCa susceptibility variants in whole exome sequencing data from familial ...

Journal: :Journal of lipid research 1992
M Reina J D Brunzell S S Deeb

The molecular basis of familial chylomicronemia (type I hyperlipoproteinemia), a rare autosomal recessive trait, was investigated in six unrelated individuals (five of Spanish descent and one of Northern European extraction). DNA amplification by polymerase chain reaction (PCR) followed by single strand conformation polymorphism (SSCP) analysis allowed rapid identification of the underlying mut...

2016
Erin K. Wagner Soumya Raychaudhuri Mercedes B. Villalonga Anuja Java Michael P. Triebwasser Mark J. Daly John P. Atkinson Johanna M. Seddon

The genetic architecture of age-related macular degeneration (AMD) involves numerous genetic variants, both common and rare, in the coding region of complement factor H (CFH). While these variants explain high disease burden in some families, they fail to explain the pathology in all. We selected families whose AMD was unexplained by known variants and performed whole exome sequencing to probe ...

Journal: :Diabetes 2008
Christine Bellanné-Chantelot Claire Carette Jean-Pierre Riveline René Valéro Jean-François Gautier Etienne Larger Yves Reznik Pierre-Henri Ducluzeau Agnès Sola Agnès Hartemann-Heurtier Pierre Lecomte Lucy Chaillous Marie Laloi-Michelin Jean-Marie Wilhem Pierre Cuny Françoise Duron Bruno Guerci Nathalie Jeandidier Helen Mosnier-Pudar Michel Assayag Danièle Dubois-Laforgue Gilberto Velho José Timsit

OBJECTIVE The clinical expression of maturity-onset diabetes of the young (MODY)-3 is highly variable. This may be due to environmental and/or genetic factors, including molecular characteristics of the hepatocyte nuclear factor 1-alpha (HNF1A) gene mutation. RESEARCH DESIGN AND METHODS We analyzed the mutations identified in 356 unrelated MODY3 patients, including 118 novel mutations, and se...

Journal: :The Journal of biological chemistry 1999
S Guerrette S Acharya R Fishel

Germline mutations in two human mismatch repair (MMR) genes, hMSH2 and hMLH1, appear to account for approximately 70% of the common cancer susceptibility syndrome hereditary nonpolyposis colorectal cancer (HNPCC). Although the hMLH1 protein has been found to copurify with another MMR protein hPMS2 as a heterodimer, their function in MMR is unknown. In this study, we have identified the physical...

Journal: :The Journal of clinical investigation 2011
Yongxing Wang Young-Ah Suh Maren Y Fuller James G Jackson Shunbin Xiong Tamara Terzian Alfonso Quintás-Cardama James A Bankson Adel K El-Naggar Guillermina Lozano

The transcription factor p53 is a tumor suppressor. As such, the P53 gene is frequently altered in human cancers. However, over 80% of the P53 mutations found in human cancers are missense mutations that lead to expression of mutant proteins that not only lack p53 transcriptional activity but exhibit new functions as well. Recent studies show that restoration of p53 expression leads to tumor re...

Journal: :The Journal of clinical endocrinology and metabolism 2001
J C Achermann M Ito B L Silverman R L Habiby S Pang A Rosler J L Jameson

DAX-1 is an orphan nuclear receptor that plays a key role in the development and function of the adrenal gland and hypothalamic-pituitary gonadal axis. Mutations in the gene encoding DAX-1 result in X-linked adrenal hypoplasia congenita (AHC). Affected boys typically present with primary adrenal failure in infancy or childhood and hypogonadotropic hypogonadism at the time of puberty. The majori...

2017
Chris D Balak Jesse M Hunter Mary E Ahearn David Wiley Gennaro D'urso Lisa Baumbach-Reardon

Background: X-linked spinal muscular atrophy (XL-SMA) results from mutations in the Ubiquitin-Like Modifier Activating Enzyme 1 ( UBA1). Previously, four novel closely clustered mutations have been shown to cause this fatal infantile disorder affecting only males. These mutations, three missense and one synonymous, all lie within Exon15 of the UBA1 gene, which contains the active adenylation do...

Journal: :American journal of human genetics 2011
Abel González-Pérez Nuria López-Bigas

Several large ongoing initiatives that profit from next-generation sequencing technologies have driven--and in coming years will continue to drive--the emergence of long catalogs of missense single-nucleotide variants (SNVs) in the human genome. As a consequence, researchers have developed various methods and their related computational tools to classify these missense SNVs as probably deleteri...

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