نتایج جستجو برای: phenotype

تعداد نتایج: 159498  

Fertility reduction due to sub-fertile males is a major concern in breeder flocks. Phenotypic traits of broiler breeder males and their relationships with fertility can be used as reliable indicators for identification and removal of sub-fertile males from the breeder flocks. This study was conducted to investigate semen traits (semen volume, sperm motility, sperm viability and sperm count) and...

Journal: :Biodesign research 2023

Modulating the extracellular matrix microenvironment is critical for achieving desired macrophage phenotype in immune investigations or tumor therapy. Combining de novo protein design and biosynthesis techniques, herein, we designed a biomimetic polypeptide self-assembled nano-immunomodulator to trigger activation of specific phenotype. It was intended be made up (​GGS​GGP​GGG​PAS​AAA​NSA​SRA​T...

Journal: :iranian rehabilitation journal 0
kimia kahrizi university of social welfare and rehabilitation sciences, teran, iran. neda moradin university of social welfare and rehabilitation sciences, teran, iran. mojtaba azimian university of social welfare and rehabilitation sciences, teran, iran. bahareh shojasaffar university of social welfare and rehabilitation sciences, teran, iran. kaveh alavi kariminejad-najmabadi pathology & genetics center, tehran, iran. shahriar nafisi shariati hospital, tehran, iran.

objectives: myotonic dystrophy type i (dm1) is a dominantly inherited disorder with a multisystemic pattern affecting skeletal muscle, heart, eye, endocrine and central nervous system. dm1 is associated with the expansion and instability of ctg repeat in the 3' untranslated region of the myotonic dystrophy protein kinase (dmpk) gene located on chromosome 19q13.3. the aim of this study was ...

Journal: :Journal of Investigative Dermatology 2021

Brooke-Spiegler syndrome (BSS; OMIM 605041) is a rare monogenic skin disease characterized by the development of appendage tumors caused mutations in cylindromatosis (CYLD) gene. Despite described phenotypes and reports underlying CYLD mutations, it has been difficult to establish genotype–phenotype correlations BSS. We recently investigated two BSS pedigrees (Hungarian with Bukovinian origin A...

Journal: :Indian Journal of Science and Technology 2017

Journal: :European Journal of Clinical Pharmacology 2008

Journal: :Archives of Neurology 2006

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید