نتایج جستجو برای: lack gene

تعداد نتایج: 1385843  

Journal: :iranian journal of applied animal science 2013
a. javanmard s.r. miraei ashtiani a. torkaman zehi m. moradi shahrbabak

the objective of the present study was to determine polymorphism within the promoter region of somatotropin receptor genes in indigenous sistani cattle (bos indicus) and associations between this polymorphism and breeding value of birth weight. the pedigree structure was included by considering 1173 animals with 600 progeny birth weight data obtained from a zhark breeding station in sistan and ...

Journal: :iranian journal of basic medical sciences 0
hossein ayatollahi cancer molecular pathology research center, ghaem hospital, faculty of medicine, mashhad university of medical sciences, mashhad, iran mohammad rafiee faculty of medicine, mashhad university of medical sciences, mashhad, iran mohammad-reza keramati cancer molecular pathology research center, ghaem hospital, faculty of medicine, mashhad university of medical sciences, mashhad, iran mahdi balali-mood medical toxicology research center, imam reza hospital, faculty of medicine, mashhad university of medical sciences, mashhad, iran ali asgharzadeh faculty of medicine, mashhad university of medical sciences, mashhad, iran mohammad hadi sadeghian cancer molecular pathology research center, ghaem hospital, faculty of medicine, mashhad university of medical sciences, mashhad, iran

objective(s):sulfur mustard (sm) was used by the iraqi army against the iranian troops in the iran-iraq war from 1983–1988. this chemical gas affects different organs including the skin, lungs and the hematopoietic system. any exposure to sm increases the risk of chromosomal breaking, hyperdiploidy and hypodiploidy. studies have shown that the risk for acute myeloblastic and lymphoblastic leuke...

Journal: :gene, cell and tissue 0
farah talebi milad genetic counseling center, ahvaz, ir iran farideh ghanbari department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, ir iran; department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, ir iran. tel/fax: +98-6136233884 javad mohammadi asl department of medical genetics, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

introduction oculocutaneous albinism (oca) is a genetically heterogeneous autosomal recessive genetic disorder that is characterized by reduced or completely absent pigmentation in the hair, skin, and eyes. conclusions a novel homozygous mutation, the deletion of exons 1 - 5 on the tyr gene, was found on the molecular genetic testing of this patient. exon 1 - 5 deletion on tyr causes a lack of ...

2009
Martin Smits Alea M. Fairchild Pieter M. A. Ribbers Koen Milis Erik van Geel

A long running challenge in both large and small organizations has been aligning information systems services with business needs. Good alignment is assumed to lead to good business results, but there is a need for good instruments to assess strategic alignment and business success in practice. Based on existing information management theories, we develop the I-Fit model and the I-Fit tool. The...

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