نتایج جستجو برای: hereditary

تعداد نتایج: 84275  

Journal: :Theoretical Computer Science 2023

Distance-hereditary graphs are in important graph class theory, as they well-placed the hierarchy and permit many algorithmic results. We investigate structural advantages of a directed version this well-researched class. Since previously defined distance-hereditary digraphs do not recursive structure, we define twin-distance-hereditary graphs, which can be constructed by several twin pendant v...

Journal: :genetics in the 3rd millennium 0
hossein najmabadi mojgan babanejad maryam beheshtian fariba ardalani hossein daghagh nooshin nikzat

hearing loss (hl) is the most common communication disorder affecting about 1/1000 births worldwide caused by environmental or genetic factors. about 30-50% is attributed to genetic factors and till now more than 85 genes have been implicated in non-syndromic hl. in iran, hl is second to intellectual disability as the most common disability, affecting 1 of every 166 persons. about 15 years ago ...

Journal: :iranian rehabilitation journal 0
seyyedeh reyhaneh amini faculty of rehabilitation sciences, tehran university of medical sciences, tehran, iran. mohammad kamali rehabilitation research center, faculty of rehabilitation sciences, tehran university of medical sciences, tehran, iran.

objectives: the prevalence of consanguineous marriage is about 30 % in iran and this can increase the probability of incidence of genetic impairments such as hearing impairments. hearing impairment in comparison with other hereditary disorders is the most incident. the purpose of this survey is to identify the prevalence of consanguinity among the parents of sensoryneural hearing impaired stude...

Journal: :jundishapur journal of microbiology 0
samia siddique department of chemistry, government college university lahore, lahore, pakistan quratulain syed food and biotechnology research center, pcsir laboratories complex, ferozpur lahore, lahore, pakistan ahmad adnan department of chemistry, government college university lahore, lahore, pakistan fahim ashraf qureshi office of research, innovation and commercialization, comsats institute of information and technology, islamabad, pakistan; office of research, innovation and commercialization, comsats institute of information and technology, islamabad, pakistan. tel: +92-3334101261, fax: +92-519247008

conclusions: the hereditary stability analysis of the uv mentioning 45 minutes revealed the uv exposure time for mutants and 3 represented the colony taken from the plate irradiated for 45 minutes mutant showed that the production of avermectin b1b remained constant and no reverse mutation occurred after 15 generations. results: avermectin b1b-hyper-producing mutant, produced using these three ...

Journal: :international journal of hematology-oncology and stem cell research 0
mehrdad payandeh medical biology research center, kermanshah university of medical science, kermanshah, iran. hoshang yousefi blood transfusion research center, high institue for research and education in transfusion medicine,science, kermanshah, iran. mohammad erfan zare medical biology research center, kermanshah university of medical science, kermanshah, iran; student atefeh nasir kansestani medical biology research center, kermanshah university of medical science, kermanshah, iran; student zohreh rahimi medical biology research center, kermanshah university of medical science, kermanshah, iran; departm dariush pourmand department of medical lab science, paramedicine faculty, kermanshah university of medical science, kermanshah, iran

introduction: the main inhibitors of coagulation pathway are antithrombin (at), protein c and protein s. these inhibitors are necessary to prevent thromboembolism. hereditary deficiency of inhibitors is the main cause of alteration in balance between the anti-clotting and the formation of thrombin. patients with this abnormality are susceptible to venous thromboembolism (vte). two major clinica...

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1997

ژورنال: پژوهش در پزشکی 2009
زالی1،, نرگس, محبی1،, سیدرضا, زالی1, محمدرضا, منتظرحقیقی*1،, مهدی, مولایی1،, مهسا,

Abstract Background: Hereditary non-polyposis colorectal cancer is the most common cause of early onset of hereditary colorectal cancer. In the majority of Hereditary non-polyposis colorectal cancer families, microsatellite instability and germline mutation in one of the DNA mismatch repair genes in clouding MSH2, MLH1, MSH6 and PMS2 are found. The Objective of this study was to determine th...

ژورنال: Iranian Rehabilitation Journal 2004
Lotfi , Younes, Mehrkian, Saeideh,

Consanguineous marriage is strongly favored in many large human populations. In the most parts of south Asia, consanguineous marriage account for 20%  to over 50% of the general population. The effect of consanguinity on hereditary deafness has been well studied and documented. Many authors have suggested that approximately one half  of sensory neural hearing loss in children can be attributed ...

Journal: :Transformation Groups 2023

Given a quasi-hereditary superalgebra A, the first author and R. Muth have defined generalized Schur bi-superalgebras TA(n) proved that these algebras are again quasi-hereditary. In particular, comes with family of standard modules. Developing work Donkin Mathieu on good filtrations, we prove tensor product modules over has filtration.

Journal: :Graphs and Combinatorics 2023

A graph is said to be distance-hereditary if the distance function in every connected induced subgraph same as itself. We prove that ordinary Weisfeiler–Leman algorithm tests isomorphism of any two graphs one them distance-hereditary; more precisely, dimension class finite equal 2. The previously best known upper bound for was 7.

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