نتایج جستجو برای: inheritance and pathogenecity

تعداد نتایج: 16831145  

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 ...

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.

Journal: :International Journal of Molecular Sciences 2023

The Special Issue “Protein-Based Infection, Inheritance, and Memory” includes a set of experimental review papers covering different aspects protein memory, infection, inheritance [...]

A. Seliga J. Siran

We prove a continuity inheritance property for super- and sub-additive transformations of non-negative continuous multivariate functions defined on the domain of all non-negative points and vanishing at the origin. As a corollary of this result we obtain that super- and sub-additive transformations of continuous aggregation functions are again continuous aggregation functions.

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...

Journal: :iranian journal of public health 0
mohammadtaghi akbari dept. of medical genetics, faculty of medical sciences, tarbiat modares university, tehran, iran and tehran medical genetics laboratory, taleghani ave, tehran, iran. mojgan ataei-kachoui tehran medical genetics laboratory, taleghani ave, tehran, iran.

lamellar ichthyosis is one form of congenital autosomal recessive ichthyosis. to date, seven causative genes for arci have been identified. to understand further the genetic spectrum of the disease, we analyzed a four-generation iranian family with arci that had observable inheritance. exome sequencing data for one of the affected individuals with ichthyosis from a consanguineous iranian family...

Journal: :genetics in the 3rd millennium 0
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Journal: : 2022

The article is devoted to clarifying the essence of phenomenon dormant inheritance in law. It has been concluded that right ownership inherited property acquired by heir retrospectively from time was opened, regardless legal regime property. However, until moment state registration ownership, limited his/her ability dispose real estate, particular alienating it. this limitation does not at all ...

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