Výsledky vyhledávání - "Anwar Madlool Al-janabi"

Akademický článek

Association of methyltetrahydrofolate reductase gene mutation, homocysteine level with semen quality of Iraqi infertile males

Autor: Anwar Madlool Al-janabi, Salih Mahdi Al-Khafaji, Shehab Ahmed Faris

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-7 (2022)

Abstract Background Infertility is very common condition and almost 50% of cases are due to male factors. Several genetic and environmental factors are responsible for the poor quality and reduced number of sperms in several cases of infertility. The

Externí odkaz: https://doaj.org/article/a5d960dfef644080872f07501572c759

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The Common polymorphisms in P21/WAF1 and MDM2 genes as a risk factor for susceptibility and poor prognosis of non-small cell lung cancer in Iraqi population

Autor: Anwar Madlool Al-Janabi, Salih Mahdi Al-Khafaji, Maher Fenjan Taher

Background: Cyclin-dependent kinase inhibitor (P21/WAFI) and murine double minute 2 (MDM2) genes regulate cell growth. In malignant tumors, altered expression of these gene products is associated with poor prognosis. Current study aimed to investigat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d47594a57463ba3ad98fd19f0e564dd9
https://doi.org/10.21203/rs.3.rs-2508295/v1

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Manuscript title The Common polymorphisms in P21/WAF1 and MDM2 genes as a risk factor for susceptibility and poor prognosis of non-small cell lung cancer in Iraqi population

Autor: Anwar Madlool Al-janabi, Salih Mahdi Al-Khafaji, Maher Fenjan Al-Saadi

Background: Cyclin dependent kinase inhibitor (P21/WAFI) and murine double minute 2 (MDM2) participate in the cell growth regulation. In malignant tumors has been found altered expression of these gene products and has been associated with poor progn

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f4114a7cca36ad017628d9fe49dd03be
https://doi.org/10.21203/rs.3.rs-1766387/v1

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Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population

Autor: Anwar Madlool, Al-Janabi, Habeeb Shuhaib, Ahmmed, Salih Mahdi, Al-Khafaji

Publikováno v: Journal of Medicine and Life

Deafness is a total or partial hearing loss that may appear at any age and with different degrees of severity. Approximately 50% of hearing loss have a genetic origin, and among them, non-syndromic sensorineural deafness represents about 70% of the c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a7a1f41e79141c7bdb7d4ee73aba67ee
https://pubmed.ncbi.nlm.nih.gov/35126756

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Connexin 26 (GJB2) Gene Mutations Linked With Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in Iraqi Population

Autor: Anwar Madlool Al-janabi, Salih M. Al-Khafaji, Habeeb Shuhaib Ahmmed

Background:Deafness is a total or partial hearing loss that may appear at any ages with different degrees of severity. Approximately 50% of hearing loss have a genetic origin, among them, the nonsyndromic sensorineural deafness represents about 70% o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f1c1854426aad743c4e6f0c78734edd
https://doi.org/10.21203/rs.3.rs-270492/v2

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Relevance of Connexin 26 (GJB2) Gene Mutations With Congenital Nonsyndromic Sensorineural Hearing Loss in Lraqi Deafness Patients

Autor: Salih M. Al-Khafaji, Anwar Madlool Al-janabi, Habeeb Shuhaib Ahmmed

Objective: This study aimed to detect the frequency of the three most common mutations of GJB2 in nonsyndromic sensorineural deafness for Iraqi population.Method: The current case-control study was conducted from January 2018 to November 2019 at ENT

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::47d8149995caa0beac1f90812f8700fe
https://doi.org/10.21203/rs.3.rs-139090/v1

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