نتایج جستجو برای: 26 polymorphic loci and 27 mutations

تعداد نتایج: 16904322  

Journal: :Protist 2013
Sylvie V M Tesson Christophe Legrand Cock van Oosterhout Marina Montresor Wiebe H C F Kooistra Gabriele Procaccini

The diatom Pseudo-nitzschia multistriata exhibits a diplontic life cycle composed of an extensive phase of vegetative cell division and a brief phase of sexual reproduction. To explore genotypic stability, we genotyped seven polymorphic microsatellite loci in 26 monoclonal strains over 3-16 months in a culture maintenance regime. Moreover, to assess inheritance patterns of the microsatellite al...

حسنی تسیه, سیده فاطمه, سمیع زاده لاهیجی, حبیب الله , شعاعی دیلمی, مرداویج ,

In present study IRAP and REMAP markers were used to assess genetic diversity levels in 45 genotypes of different types of tobacco germplasm, including burley, flue-cured and oriental tobacco that out of 20 composition primers, 5 IRAP primersand 9 REMAP primers produced scorable and polymorphic banding patterns. Totally from 188 amplified loci, 153 loci were polymorph. RTR-10 and RTR-1 with 22 ...

زمانی, محمد, دانشی, احمد, ریاض‌الحسینی, یاسر, ریحانی‌فر, فرحناز, نجم‌آبادی, حسین, کهریزی, کیمیا, محسنی, مرضیه ,

    Background & Aim: Hereditary hearing loss(HHL) affects one in 1000-2000 newborns and more than 50% of these cases have a genetic base. About 70% of HHL are nonsyndromic with autosomal recessive forms accounting for 85% of the genetic load. Different genes have been reported to be involved, but mutations in GJB2 gene at DFNB1 locus have been established as the basis of autosomal recessive no...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
J W Fondon G M Mele R I Brezinschek D Cummings A Pande J Wren K M O'Brien K C Kupfer M H Wei M Lerman J D Minna H R Garner

A computational system for the prediction of polymorphic loci directly and efficiently from human genomic sequence was developed and verified. A suite of programs, collectively called POMPOUS (polymorphic marker prediction of ubiquitous simple sequences) detects tandem repeats ranging from dinucleotides up to 250 mers, scores them according to predicted level of polymorphism, and designs approp...

2009
Fábio Pinheiro Clarisse Palma-Silva Fábio de Barros Salvatore Cozzolino

In this study we tested the cross-amplification of 33 microsatellite loci previously developed for two closely related Neotropical orchid genera (Epidendrum and Laelia). A set of ten loci were polymorphic across five examined species (20 individuals each) with 2 to 15 alleles per locus. The mean expected and observed heterozygosity (average across species) ranged from 0.34 to 0.82 and from 0.27...

Journal: :Journal of medical genetics 1987
T F Wienker G Hudek S Bissbort A Mayerová G Mauff K Bender

A kindred segregating for Van der Woude syndrome (VWS) through five generations is described. Biochemical and serological phenotypes at 36 polymorphic marker loci have been determined, of which 27 were informative for linkage analysis to the VWS gene (LIPED 3 computer programme). Lod scores are reported and show exclusion of close linkage for most of the marker loci. Only VWS:Duffy (Fy) resulte...

Journal: :Genetics 1975
D A Levin

Twenty enzyme loci were studied in 44 Illinois populations of Oenothera biennis; four were polymorphic. Most of the variation was distributed between populations. Fifty-nine percent of the populations had one genotype, 27% two genotypes and the remaining 16% from three to five genotypes; the average was 1.50. The proportion of genetic diversity present in single populations is.38 of that presen...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1972
D A Levin G P Howland E Steiner

Genic allozyme polymorphism and heterozygosity was studied in a large population of the evening primrose, Oenothera biennis, growing in North Haven, Connecticut. This species is a permanent structural heterozygote for the entire complement of 14 chromosomes, and is thus capable of accumulating and maintaining genic heterozygosity. A total of 11 protein species were examined, and these were judg...

M.R. Noori-Daloii

The incidence of pre-lingual hearing loss (HL) is about 1 in 1000 neonates. More than 60% of cases are inherited. Non-syndromic HL (NSHL) is extremely heterogeneous: more than 130 loci have been identified so far. The most common form of NSHL is the autosomal recessive form (ARNSHL). In this study, a cohort of 36 big ARNSHL pedigrees with 4 or more patients from 7 provinces of Iran was investig...

تیموری, حسین, مجتبوی نائینی, مرجان, معتمدی, سمیرا, هاشم زاده چالشتری, مرتضی,

Background and Objective: TMC1 gene mutations are known as the most common causes of autosomal recessive non-syndromic hearing loss (ARNSHL) in different populations. According to large size of the TMC1 gene and the large number of identified mutations in this gene, application of polymorphic markers is suggested for carrier detection and prenatal diagnosis in families. In this study, informati...

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