نتایج جستجو برای: founder effect

تعداد نتایج: 1647862  

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006
Avi Orr-Urtreger Anat Bar-Shira Dani Bercovich Noa Matarasso Uri Rozovsky Serena Rosner Sonya Soloviov Gad Rennert Luna Kadouri Ayala Hubert Hanna Rennert Haim Matzkin

Epidemiologic and genetic studies support the considerable effect of heritable factors on prostate tumorigenesis, although to date, no unequivocal susceptibility gene has been identified. The extensive study of RNASEL in prostate cancer patients worldwide has yielded conflicting results. We reevaluated the role of the RNASEL 471delAAAG Ashkenazi founder mutation in 1,642 Ashkenazi patients with...

2015
Samiah A Al-Zaidy Vinod Malik Kelley Kneile Xiomara Q Rosales Ana Maria Gomez Sarah Lewis Sayaka Hashimoto Julie Gastier-Foster Peter Kang Basil Darras Louis Kunkel Jose Carlo Zarife Sahenk Steven A Moore Robert Pyatt Jerry R Mendell

Limb-girdle muscular dystrophy type 2C (LGMD2C) is considered one of the severe forms of childhood-onset muscular dystrophy. The geographical distribution of founder mutations in the SGCG gene has a prominent effect on the prevalence of LGMD2C in certain populations. The aim of this study was to confirm the hypothesis that the c.787G>A (p.E263K) mutation in the SGCG gene is a founder mutation a...

Journal: :Blood 2004
Enli Liu Melanie J Percy Christopher I Amos Yongli Guan Sanjay Shete David W Stockton Mary F McMullin Lydia A Polyakova Sonny O Ang Yves D Pastore Katerina Jedlickova Terry R J Lappin Victor Gordeuk Josef T Prchal

The first congenital defect of hypoxia-sensing homozygosity for VHL 598C>T mutation was recently identified in Chuvash polycythemia. Subsequently, we found this mutation in 11 unrelated individuals of diverse ethnic backgrounds. To address the question of whether the VHL 598C>T substitution occurred in a single founder or resulted from recurrent mutational events in human evolution, we performe...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2007
R Ferla V Calò S Cascio G Rinaldi G Badalamenti I Carreca E Surmacz G Colucci V Bazan A Russo

BRCA1 and BRCA2 germline mutations contribute to a significant number of familial and hereditary breast and/or ovarian cancers. The proportion of high-risk families with breast and/or ovarian cancer cases due to mutations in these tumor suppressor genes varies widely among populations. In some population, a wide spectrum of different mutations in both genes are present, whereas in other groups ...

Journal: :Clinical genetics 2015
Y Goldberg I Barnes-Kedar I Lerer N Halpern M Plesser A Hubert L Kadouri H Goldshmidt I Solar H Strul G Rosner H N Baris T Peretz Z Levi R Kariv

Diagnosis of Lynch syndrome (LS) may be complex. Knowledge of mutation spectrum and founder mutations in specific populations facilitates the diagnostic process. Aim of the study is to describe genetic features of LS in the Israeli population and report novel and founder mutations. Patients were studied at high-risk clinics. Diagnostics followed a multi-step process, including tumor testing, ge...

Journal: :Current Biology 2010
Bert De Rybel Valya Vassileva Boris Parizot Marlies Demeulenaere Wim Grunewald Dominique Audenaert Jelle Van Campenhout Paul Overvoorde Leentje Jansen Steffen Vanneste Barbara Möller Michael Wilson Tara Holman Gert Van Isterdael Géraldine Brunoud Marnik Vuylsteke Teva Vernoux Lieven De Veylder Dirk Inzé Dolf Weijers Malcolm J. Bennett Tom Beeckman

BACKGROUND Lateral roots are formed at regular intervals along the main root by recurrent specification of founder cells. To date, the mechanism by which branching of the root system is controlled and founder cells become specified remains unknown. RESULTS Our study reports the identification of the auxin regulatory components and their target gene, GATA23, which control lateral root founder ...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2004
G Cipollini S Tommasi A Paradiso P Aretini F Bonatti I Brunetti M Bruno G Lombardi F Schittulli E Sensi M Tancredi G Bevilacqua M A Caligo

Genetic linkage studies have led to the identification of highly penetrant genes as the possible cause of inherited cancer risk in many cancer-prone families. Most women with a family history of breast/ovarian cancer have tumors characterized by alterations in particular genes, mainly BRCA1 and BRCA2, but also CHK2, ATM, STK11 and others. This paper examines the BRCA1 and BRCA2 genes, focusing ...

Journal: :American journal of human genetics 2003
Neil Howell Roelof-Jan Oostra Piet A Bolhuis Liesbeth Spruijt Lorne A Clarke David A Mackey Gwen Preston Corinna Herrnstadt

The complete mitochondrial DNA (mtDNA) sequences for 63 Dutch pedigrees with Leber hereditary optic neuropathy (LHON) were determined, 56 of which carried one of the classic LHON mutations at nucleotide (nt) 3460, 11778, or 14484. Analysis of these sequences indicated that there were several instances in which the mtDNAs were either identical or related by descent. The most striking example was...

Journal: :Molecular ecology 2009
J Scott Keogh

Founder populations in reintroduction programmes can experience a genetic bottleneck simply because of their small size. The influence of reproductive skew brought on by polygynous or polyandrous mating systems in these populations can exacerbate already difficult conservation genetic problems, such as inbreeding depression and loss of adaptive potential. Without an understanding of reproductiv...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Michael DeGiorgio Mattias Jakobsson Noah A Rosenberg

Studies of worldwide human variation have discovered three trends in summary statistics as a function of increasing geographic distance from East Africa: a decrease in heterozygosity, an increase in linkage disequilibrium (LD), and a decrease in the slope of the ancestral allele frequency spectrum. Forward simulations of unlinked loci have shown that the decline in heterozygosity can be describ...

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