نتایج جستجو برای: chromosomal rearrangement

تعداد نتایج: 71324  

2017
Claudia Gebert Lauren Correia Zhenhu Li Howard T Petrie Paul E Love Karl Pfeifer

V-(D)-J recombination generates the antigen receptor diversity necessary for immune cell function, while allelic exclusion ensures that each cell expresses a single antigen receptor. V-(D)-J recombination of the Ig, Tcrb, Tcrg and Tcrd antigen receptor genes is ordered and sequential so that only one allele generates a productive rearrangement. The mechanism controlling sequential rearrangement...

2017
Guillaume Martin Françoise Carreel Olivier Coriton Catherine Hervouet Céline Cardi Paco Derouault Danièle Roques Frédéric Salmon Mathieu Rouard Julie Sardos Karine Labadie Franc-Christophe Baurens Angélique D’Hont

Most banana cultivars are triploid seedless parthenocarpic clones derived from hybridization between Musa acuminata subspecies and sometimes M. balbisiana. M. acuminata subspecies were suggested to differ by a few large chromosomal rearrangements based on chromosome pairing configurations in intersubspecies hybrids. We searched for large chromosomal rearrangements in a seedy M. acuminata ssp. m...

2016
Inga Grünewald Marcel Trautmann Alina Busch Larissa Bauer Sebastian Huss Petra Schweinshaupt Claudia Vollbrecht Margarete Odenthal Alexander Quaas Reinhard Büttner Moritz F. Meyer Dirk Beutner Karl-Bernd Hüttenbrink Eva Wardelmann Markus Stenner Wolfgang Hartmann

Salivary duct carcinoma (SDC) is an aggressive adenocarcinoma of the salivary glands associated with poor clinical outcome. SDCs are known to carry TP53 mutations in about 50%, however, only little is known about alternative pathogenic mechanisms within the p53 regulatory network. Particularly, data on alterations of the oncogenes MDM2 and CDK4 located in the chromosomal region 12q13-15 are lim...

Journal: :Journal of medical genetics 1997
P Stankiewicz E Kostyk E Bocian H Stańczak J Parczewska E Piatkowska T Mazurczak J J Pietrzyk

A familial four breakpoint complex chromosomal rearrangement involving chromosomes 9, 10, and 11 was ascertained through a child with dysmorphic features, hypertrophic cardiomyopathy, and hypotonia. A cryptic insertion, invisible in G banded chromosomes was identified by fluorescence in situ hybridisation (FISH) using chromosome specific libraries. Possible mechanisms of its formation as well a...

Journal: :Trends in ecology & evolution 2001
L H. Rieseberg

Several authors have proposed that speciation frequently occurs when a population becomes fixed for one or more chromosomal rearrangements that reduce fitness when they are heterozygous. This hypothesis has little theoretical support because mutations that cause a large reduction in fitness can be fixed through drift only in small, inbred populations. Moreover, the effects of chromosomal rearra...

Journal: :Genome research 2002
Klaas Vandepoele Yvan Saeys Cedric Simillion Jeroen Raes Yves Van De Peer

It is expected that one of the merits of comparative genomics lies in the transfer of structural and functional information from one genome to another. This is based on the observation that, although the number of chromosomal rearrangements that occur in genomes is extensive, different species still exhibit a certain degree of conservation regarding gene content and gene order. It is in this re...

Journal: :journal of physical & theoretical chemistry 2005
saeed taghvaei-ganjali hassan kabiri-fard

thermal rearrangement of 7,7-dichloro-[a,c]-dibenzo-[4,1,0]-bicycloheptane (1) to 5,6-dichloro-5hdibenzo-[a,c]-cycloheptene (2) was studied in the solid phase and in solvents with different polarities. thefirst-order constants at various temperatures for the rearrangement process were evaluated from theabsorption time data. the activation parameters for this rearrangement were obtained from the...

Journal: :The Journal of clinical endocrinology and metabolism 1998
C H Lee L S Hsu C W Chi G D Chen A H Yang J Y Chen

The activation of RET protooncogene, through chromosomal translocation, is unique to papillary thyroid carcinomas. Rearrangement of the RET kinase domain to 3 partner genes has been described, of which the RET/PTC1 is the most common. To investigate the frequency of RET rearrangement in Chinese papillary thyroid carcinomas, we have performed RT-PCR to amplify specific RET/PTC transcripts. Among...

2004
J J Pietrzyk

A familial four breakpoint complex chromosomal rearrangement involving chromosomes 9, 10, and 11 was ascertained through a child with dysmorphic features, hypertrophic cardiomyopathy, and hypotonia. A cryptic insertion, invisible in G banded chromosomes was identified by fluorescence in situ hybridisation (FISH) using chromosome specific libraries. Possible mechanisms of its formation as weli a...

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