نتایج جستجو برای: familial translocations

تعداد نتایج: 61491  

Journal: :Journal of Ecology 2021

Anthropogenic climate warming is undisputed and yet, there much that unknown regarding biological impacts of changing temperature precipitation, the management options presented as solutions to biodiversity losses—such translocations plants seeds—are often controversial. This Special Focus presents five new studies two recently published articles in Journal Ecology Ecological Solutions Evidence...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Emma R Woodward Christopher Ricketts Pip Killick Sophie Gad M R Morris Fred Kavalier Shirley V Hodgson Sophie Giraud Brigitte Bressac-de Paillerets Cyril Chapman Bernard Escudier Farida Latif Stéphane Richard Eamonn R Maher

PURPOSE Familial renal cell carcinoma (RCC) is genetically heterogeneous. The most common histopathologic subtype of sporadic and familial RCC is clear cell (cRCC) and von Hippel-Lindau (VHL) disease is the most common cause of inherited cRCC. Familial cRCC may also be associated with chromosome 3 translocations and has recently been described in patients with Birt-Hogg-Dube (BHD) syndrome, cau...

Journal: :journal of biotechnology and health sciences 0
reza najafipour cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran javad ansari cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran manijeh jalilvand cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran sahar moghbelinejad cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran; cellular and molecular research center, qazvin university of medical sciences, qazvin, ir iran. tel: +98-2813336001, fax: +98-2813324970

background chromosomal abnormality plays an important role in different types of miscarriages. objectives the present study was designed to investigation chromosomal anomalies in three groups of couples with recurrent abortion (ra), spontaneous abortion (sa) and still birth (sb). patients and methods in this retrospective study, the frequency of chromosomal aberrations was investigated among 26...

Journal: :acta medica iranica 0
p. fard-esfahani p. mohammadi-torbati s. khatami s. zeinali m. taghikhani m. allahyari

familial defective apolipoprotein (apo) b 100 (fdb) causes early-onset coronary heart diseases (chd). it is produced by r3500q mutation of the apob gene resulting in decreased binding of ldl to ldl receptor. we screened the apo b gene for r3500q mutation in 130 hypercholesterolemic patients, among whom 30 patients met criteria of familial hypercholesterolemia (fh). the prevalence of r3500q alle...

Journal: :Voprosy onkologii 2022

The discovery of recurrent EGFR mutations, ALK and ROS1 translocations, together with the development effective targeted drugs, has become a real breakthrough in treatment lung cancer. Molecular diagnosis alteration these genes already mandatory part evaluating patients non-small cell paper presents combined diagnostic approach, which allows identification known chimeric transcripts new variant...

Journal: :middle east journal of cancer 0
abolfazl movafagh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran mehrdad hashemi associate professor of molecular genetics, department of genetics, islamic azad university,tehran medical branch,tehran,iran mojtaba ghadiani department of internal medicine/oncology, taleghani hospital, shahid beheshti university of medical sciences, tehran, iran reza mirfakhraei department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran hossein darvish department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran davood zare abdollahi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran

background : according to the literature, there are a number of chronic and acute myeloid leukemias with unique, complex chromosome translocations. this study aims to conduct a brief review of the incidence of complex chromosome translocations in myeloid leukemia and reports a case of myeloid leukemia with complex chromosome translocations. methods :we conducted a web-based search for all peer ...

Journal: :Genome Biology 2001

Journal: :Nature Biotechnology 2011

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