نتایج جستجو برای: transgene inheritance

تعداد نتایج: 66466  

ژورنال: :genetics in the 3rd millennium 0
محمد حسن کریمی نژاد mohammad hassan kariminejad

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 ...

ژورنال: حقوق پزشکی 2017
مسجد سرائی, حمید, نظری, اعظم,

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...

Journal: :American journal of physiology. Renal physiology 2001
Y Ding C D Sigmund

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...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1996
K W Dobie M Lee J A Fantes E Graham A J Clark A Springbett R Lathe M McClenaghan

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...

Journal: :iranian journal of child neurology 0
seyyed hasan tonekaboni associate professor of pediatric neurology, pediatric neurology research center, shahid beheshti university of medical sciences (sbmu),tehran

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...

Journal: :iranian journal of child neurology 0
mohammad ghofrani 1. pediatric neurology research center, shahid behesti university of medical sciences, tehran, iran 2. department of pediatric neurology, pediatric neurology center of excellence, mofid children hospital, faculty of medicine, shahid behesti university of

pls see pdf.

ژورنال: علوم آب و خاک 1999
خدامباشی, محمود , شارما, بالرام ,

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...

2016
Jennifer R. Mandel Adam J. Ramsey Massimo Iorizzo Philipp W. Simon

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...

Journal: :iranian journal of neurology 0
abbas tafakhori department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. vajiheh aghamollaii department of neurology, school of medicine, roozbeh hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. sara faghihi-kashani department of neurology, school of medicine, tehran university of medical sciences, tehran, iran. payam sarraf department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran. laleh habibi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran.

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...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید