نتایج جستجو برای: polymorphic trinucleotide

تعداد نتایج: 27186  

2013
Durgadatta Tosh Bineet Panda Tipirisetti Nageswar Rao Arvind Babu Vishnupriya Satti Lalji Singh Lakshmi Rao

Aim: The Androgen Receptor (AR) is a ligand-dependent transcriptional activator and the AR gene contains a highly polymorphic trinucleotide repeat CAG and GGN in the first exon. Given the lack of information AR-CAG and GGN repeat polymorphism and its potential correlation with breast cancer in South Indian women, we conducted a case-control study to observe the effects of CAG & GGN repeat lengt...

Journal: :Nucleic Acids Research 2005
Ya-Hui Chang Wen-Hui Su Tso-Ching Lee Hsiao-Fang Sunny Sun Chia-Hsiang Chen Wen-Harn Pan Shih-Feng Tsai Yuh-Shan Jou

Taiwan Polymorphic Marker Database (TPMD) (http://tpmd.nhri.org.tw/) is a marker database designed to provide experimental details and useful marker information allelotyped in Taiwanese populations accompanied by resources and technical supports. The current version deposited more than 372,000 allelotyping data from 1425 frequently used and fluorescent-labeled microsatellite markers with variat...

Journal: :Clinical chemistry 2006
Youyou Zhou Josephine M S Lum Gare-Hoon Yeo Jennifer Kiing Stacey K H Tay Samuel S Chong

BACKGROUND Fragile X syndrome (FXS), the most common cause of inherited mental impairment, is most commonly related to hyperexpansion and hypermethylation of a polymorphic CGG trinucleotide repeat in the 5' untranslated region of the FMR1 gene. Southern blot analysis is the most commonly used method for molecular diagnosis of FXS. We describe a simplified strategy based on fluorescent methylati...

2013
Michael R. Hunsaker Anthony Hannan Peter Todd Abbie Renoux

It has become increasingly important that the field of behavioral genetics identifies not only the gross behavioral phenotypes associated with a given mutation, but also the behavioral endophenotypes that scale with the dosage of the particular mutation being studied. Over the past few years, studies evaluating the effects of the polymorphic CGG trinucleotide repeat on the FMR1 gene underlying ...

2012
Jonathan J. Magaña Bulmaro Cisneros

For a long time, the human genome was considered an intrinsically stable entity; however, it is currently known that our human genome contains many unstable elements consisting of tandem repeat elements, mainly Short tandem repeats (STR), also known as microsatellites or Simple sequence repeats (SSR) (Ellegren, 2000). These sequences involve a repetitive unit of 1-6 bp, forming series with leng...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Andrew John Li Beth Young Karlan

PURPOSE Preoperative thrombocytosis (platelet count > 400 x 10(9)/L) at initial exploration for epithelial ovarian carcinoma is associated with decreased surgical cytoreducibility and poor survival. Platelets express androgen receptor (AR), which contains a polymorphic CAG trinucleotide repeat sequence of which the length inversely correlates with AR transactivation function. We hypothesized th...

Journal: :Human molecular genetics 1999
R P Grewal G Cancel E P Leeflang A Dürr M S McPeek D Draghinas X Yao G Stevanin M O Alnot A Brice N Arnheim

Segregation distortion has been reported to occur in a number of the trinucleotide repeat disorders. On the basis of a sperm typing study performed in patients of Japanese descent with Machado-Joseph disease (MJD), it was reported that disease alleles are preferentially transmitted during meiosis. We performed a sperm typing study of five MJD patients of French descent and analysis of the poole...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2000
I Vuillaume P Meynieu S Schraen-Maschke A Destée B Sablonnière

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by an expanded (CAG)n repeat on the huntingtin gene. It is characterised by motor, psychiatric and cognitive disturbances. Diagnosis can be confirmed by direct genetic testing, which is highly sensitive and specific and is now considered definitive. This study focused on 21 patients presenting with a clinical p...

Journal: :Fertility and sterility 2001
A Mifsud C K Sim H Boettger-Tong S Moreira D J Lamb L I Lipshultz E L Yong

OBJECTIVE To determine whether changes in the polymorphic trinucleotide (CAG) tract of the androgen receptor gene are associated with spermatogenic defects in patients with male infertility. DESIGN Case-control study of two ethnic groups. SETTING University referral centers for male infertility at Baylor College of Medicine, Houston, Texas, and National University Hospital, Singapore. PAR...

2015
A. B. Addisalem G. Danny Esselink F. Bongers M. J. M. Smulders

Microsatellite (or simple sequence repeat, SSR) markers are highly informative DNA markers often used in conservation genetic research. Next-generation sequencing enables efficient development of large numbers of SSR markers at lower costs. Boswellia papyrifera is an economically important tree species used for frankincense production, an aromatic resinous gum exudate from bark. It grows in dry...

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