نتایج جستجو برای: dhplc

تعداد نتایج: 390  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید چمران اهواز - دانشکده علوم 1392

مقدمه: سرطان پستان شایعترین سرطان در زنان است. سرطان پستان فامیلی10درصد کل سرطان های پستان را شامل می شوند. جهش های ارثی در دو ژن brca1 و brca2 به عنوان ژن های مستعد کننده سرطان پستان زودرس با نفوذ بالا، شانس ابتلا به این سرطان را تا 87 درصد بالا می برند. brca1و brca2 ژن های سرکوبگر تومور اند که در تعمیر dna نقش مهمی دارند. به نظر می رسد که هر جمعیت و نژادی دارای جهش های ویژه ی خود می باشد. هدف...

2004
David P. Steensma Douglas R. Higgs Chris A. Fisher Richard J. Gibbons

Acquired somatic mutations in ATRX, an X-linked gene encoding a chromatinassociated protein, were recently identified in 4 patients with the rare subtype of myelodysplastic syndrome (MDS) associated with thalassemia (ATMDS). Here we describe a series of novel point mutations in ATRX detected in archival DNA samples from marrow and/or blood of patients with ATMDS by use of denaturing high-perfor...

2010
Wei Wang Jin Jiang Yanan Zhu Jinyu Li Chongfei Jin Xingchao Shentu Ke Yao

PURPOSE To detect the underlying genetic defect in a Chinese family affected with bilateral congenital cataracts. METHODS A detailed family history and clinical data were recorded. Mutation screening was performed in the nuclear cataract-related gene by bidirectional sequencing of the amplified products. The mutation was verified by denaturing high-performance liquid chromatography (DHPLC). ...

Journal: :Clinical chemistry 2007
Stefania Stenirri Gabriella Restagno Giovanni Battista Ferrero Georgia Alaimo Luca Sbaiz Caterina Mari Lorenzo Genitori Ferrari Maurizio Laura Cremonesi

BACKGROUND Craniosynostosis, the premature fusion of 1 or more sutures of the skull, is a common congenital defect, with a prevalence of 1 in 2500 live births. Untreated progressive craniosynostosis leads to inhibition of brain growth and increased intracranial and intraorbital pressure. The heterogeneity of clinical phenotypes and the overlap of the various associated syndromes render the corr...

2015
Donatella Bianchessi Sara Morosini Veronica Saletti Maria Cristina Ibba Federica Natacci Silvia Esposito Claudia Cesaretti Daria Riva Gaetano Finocchiaro Marica Eoli

Genetic analysis of Neurofibromatosis type 1 (NF1) may facilitate the identification of patients in early phases of the disease. Here, we present an overview of our diagnostic research spanning the last 11 years, with a focus on the description of 225 NF1 mutations, 126 of which are novel, found in a series of 607 patients (513 unrelated) in Italy. Between 2003 and 2013, 443 unrelated patients ...

Journal: :Nucleic acids research 2002
Angela Gallo Emma Thomson James Brindle Mary A O'Connell Liam P Keegan

Post-transcriptional processes such as alternative splicing and RNA editing have a huge impact on the diversity of the proteome. Detecting alternatively spliced transcripts is difficult when they are rare. In addition, edited transcripts often differ from the genomic sequence by only a few nucleotides. Denaturing high performance liquid chromatography (DHPLC) is routinely used for single nucleo...

2014
Mario Geffe Lars Andernach Oliver Trapp Till Opatz

Surprisingly stable formamide rotamers were encountered in the tetrahydroisoquinoline and morphinan series of alkaloids. We investigated the hindered rotation around the amide bond by dynamic high-performance liquid chromatography (DHPLC) and kinetic measurements of the interconversion of the rotamers which can readily be separated by HPLC as well as TLC. The experimental results of the differe...

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