نتایج جستجو برای: transgene inheritance
تعداد نتایج: 66466 فیلتر نتایج به سال:
بیماری های مندلی بیماری هایی هستند که ناشی از اثرات یک ژن بر فنوتیپ فرد می باشند. انتقال آنها از نسلی به نسل دیگر همانند الگوهایی است که مندل توضیح داد. اگر ژن بیماری ها بر روی کروموزوم های جسمی (اتوزوم) قرار داشته باشد این توارث را جسمی (autosomal) و اگر بر روی کروموزوم های جنسی قرار داشته باشد آن را توارث وابسته به جنس (sex-likned) می نامند. طرح توارث بیماری ها از طریق انتقال صفات در خانواده ...
With the development of medical knowledge in the field of treatment of infertility, jurisprudence and legal issues have raised about it, among which is inheritance of fetus produced through modern fertility techniques. Given "inheritance" is a civil right of the fetus, so, the question is that what is the inheritance status of child produced through modern fertility techniques? Thus t...
We previously reported a novel transgenic model expressing human angiotensinogen from the kidney androgen-regulated protein promoter, and demonstrated sexually dimorphic expression. Herein, we investigated the hormonal regulation of this transgene. Testosterone increased transgene expression in female mice in a dose- and time-dependent manner and was not detectable 3-days after treatment was ha...
Mice carrying an ovine beta-lactoglobulin (BLG) transgene secrete BLG protein into their milk. To explore transgene expression stability, we studied expression levels in three BLG transgenic mouse lines. Unexpectedly, two lines exhibited variable levels of transgene expression. Copy number within lines appeared to be stable and there was no evidence of transgene rearrangement. In the most varia...
objective hereditary spastic paraplegia (hsp) is a degenerative disease of genetic origin affecting the corticospinal tracts in the spinal cord. there are three forms of inheritance: autosomal dominant hsp, autosomal rececive hsp and x-linked hsp. this disease is characterized by progressive spasticity of leg muscles with varying degrees of stiffness and weakness of other muscle groups. in this...
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In spite of different reports about the inheritance of cotyledon colour in lentil, the precise nature of this phenomenon is unknown. In a comprehensive study, conducted in 1993-96 on inheritance of morphological markers in lentil, two types of green colour, light green and dark-green lentils, were distinguished for the first time. The dark-green showed monogenic and the light-green showed digen...
Studies of gene flow between crops and their wild relatives have implications for both management practices for cultivation and understanding the risk of transgene escape. These types of studies may also yield insight into population dynamics and the evolutionary consequences of gene flow for wild relatives of crop species. Moreover, the comparison of genetic markers with different modes of inh...
epilepsy is one of the most common neurological disorders. studies have demonstrated that genetic factors have a strong role in etiology of epilepsy. mutations in genes encoding ion channels, neurotransmitters and other proteins involved in the neuronal biology have been recognized in different types of this disease. moreover, some chromosomal aberration including ring chromosomes will result i...
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