نتایج جستجو برای: comparative genomic hybridization

تعداد نتایج: 397000  

ژورنال: :genetics in the 3rd millennium 0
رکسانا کریمی نژاد roxsana kariminejad کیمیا نجفی kimiya najafi کیا نجفی kiya najafi آزاده مشتاق azadeh moshtagh محمد حسن کریمی نژاد mohammadhassan kariminejad شهرک غرب, میدان صنعت, شماره 1143,

پس از شرح مختصری در مورد تولد دانش سیتوژنتیک (1956) و کاربرد آن در پزشکی (1959) به عنوان آزمایش ارزنده ای برای تشخیص بیماریهای ارثی ناشی از ناهنجاریهای کروموزومی، محدودیت دامنه کارآیی آن، محققین را بر آن داشت روش های نواری b‏anding را کشف و به کار گیرند. این روش توانست بسیاری از مشکلات و محدودیت های قبلی را مرتفع نماید ولی باز در مواردی به ویژه در نمونه هایی که امکان کشت بافت مقدور نبود، همچنین...

Journal: :journal of family and reproductive health 0
jila dastan gene clinic, tehran, iran saeed reza ghaffari gene clinic, tehran, iran. vali-e-asr reproductive health research center, medical sciences/ university of tehran,iran. department of medical genetics, medical sciences/ university of tehran, tehran,iran. iranian fetal medicine foundation, tehran, iran. department of genetics and genomics, cancer research center, tehran, iran. tayebeh sabokbar department of genetics and genomics, cancer research center, tehran, iran fatemeh ramezanzadeh vali-e-asr reproductive health research center, medical sciences/ university of tehran,iran

objective: this study determined the chromosomal constitution of recurrent spontaneous abortions by comparative genomic hybridization (cgh) analysis of fetal samples. material and methods:   forty pregnant women with early recurrent pregnancy losses aged 21 to 42 years old from tehran university of medical sciences affiliated hospitals entered in this descriptive study. hibridization analysis o...

Journal: :reports of biochemistry and molecular biology 0
azadeh shojaei department of medical genetics and molecular biology, faculty of medicine, iran university of medical sciences, tehran, iran. reza ebrahimzadeh-vesal department of basic medical science, faculty of medicine, neyshabur university of medical sciences, neyshabur, iran. ali ahani mendel medical genetic laboratory, tehran, iran maryam razzaghy-azar : metabolic disorders research center, endocrinology and metabolism molecular-cellular sciences institute, iran university of medical sciences, tehran, iran; h. aliasghar hospital, iran university of medical sciences, tehran, iran. golnaz khakpour department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran. farideh ghazi tel: +98 21 88602209; fax: +98 21 88602209;

background: disorders of sex development (dsds) belong to uncommon pathologies and result from abnormalities during gonadal determination and differentiation. various gene mutations involved in gonadal determination and differentiation have been associated with gonadal dysgenesis. despite advances in exploration of genes and mechanisms involved in sex disorders, most children with severe 46,xy ...

Journal: :American Journal of Clinical Pathology 2003

نزهت, زهرا , هدایتی, مهدی ,

In situ hybridization (ISH) is a method that uses labeled complementary single strand DNA or RNA to localize specific DNA or RNA sequences in an intact cell or in a fixed tissue section. The main steps of ISH consist of: probe selection, tissue or sample preparation, pre-hybridization treatment, hybridization and washing, detection and control procedure. Probe selection is one of the important ...

Journal: :The Journal of Molecular Diagnostics 2006

Journal: :Biostatistics 2008
Robert Tibshirani Pei Wang

We apply the "fused lasso" regression method of (TSRZ2004) to the problem of "hot- spot detection", in particular, detection of regions of gain or loss in comparative genomic hybridization (CGH) data. The fused lasso criterion leads to a convex optimization problem, and we provide a fast algorithm for its solution. Estimates of false-discovery rate are also provided. Our studies show that the n...

Journal: :Mathematical biosciences 2002
Aniko Szabo Kenneth Boucher

Human solid tumors are believed to be caused by a sequence of genetic abnormalities arising in the tumor cells. The understanding of these sequences is extremely important for improving cancer treatment. Models for the occurrence of the abnormalities include linear structure and a recently proposed tree-based structure. In this paper we extend the pure oncogenetic tree model by introducing fals...

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