نتایج جستجو برای: founder effect

تعداد نتایج: 1647862  

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2015
Kyum-Yil Kwon Kuhl Huh Baik-Lin Eun Han-Wook Yoo Eric-Jan Kamsteeg Hans Scheffer Seong-Beom Koh

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) has been identified in diverse countries. However, outside of North America, North Africa, and Europe, ARSACS was recognized only in the Japanese population. Moreover, through genetic research, the disease is thought to exhibit no founder effect, except in the Quebec descent. Therefore, it is possible that ARSACS might be undere...

Journal: :Science 2012
Rory Van Tuyl Asya Pereltsvaig

Atkinson (Reports, 15 April 2011, p. 346) concluded that language originated in western Africa and that, due to a serial founder effect, languages repeatedly lost phonemes the farther they moved from the African point of origin. Independent examination of the published data tends to refute both these claims.

2012
Eric Letouzé Aliou Sow Fabien Petel Roberto Rosati Bonald C. Figueiredo Nelly Burnichon Anne-Paule Gimenez-Roqueplo Enzo Lalli Aurélien de Reyniès

Dense genotype data can be used to detect chromosome fragments inherited from a common ancestor in apparently unrelated individuals. A disease-causing mutation inherited from a common founder may thus be detected by searching for a common haplotype signature in a sample population of patients. We present here FounderTracker, a computational method for the genome-wide detection of founder mutati...

2012
Jing Chen Peter Thompson

In this paper we study some causes and consequences of founder-CEO replacements among a sample of 4,172 Danish startups created by single founders in 1999 and 2000. In contrast to the extant literature on VC-financed firms, replacements among firms in our sample are more likely among the worstand best-performing firms, and replacement is not unambiguously associated with better subsequent perfo...

Journal: :The Journal of investigative dermatology 2003
Guofang Hu Mehmet Yildirim Vahide Baysal Ozlem Yerebakan Ertan Yilmaz H Serhat Inaloz Amalia Martinez-Mir Angela M Christiano Julide Tok Celebi

Mal de Meleda is a rare form of palmoplantar keratoderma, and recently mutations in the ARS (component) B gene have been identified in families with this disease. We identified a recurrent nonsense mutation, R96X, in four families of Turkish descent. In this report, we demonstrate that these families share a common ancestral haplotype at the mal de Meleda locus, suggesting a founder effect.

Journal: :Proceedings of the National Academy of Sciences 2002

Journal: :The Dublin Journal of Medical Science 1906

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید