Zobrazeno 1 - 10
of 957
pro vyhledávání: '"S Zeinali"'
Publikováno v:
Iranian Journal of Public Health, Vol 40, Iss 2, Pp 57-66 (2011)
"nBackground: BRCA1 and BRCA2 genes have been recognized to be responsible for 20-30% of hereditary breast cancers and approximately 50% of familial breast and ovarian cancers. Therefore, the demand for BRCA1 and BRCA2 mutation screening is rapid
Externí odkaz:
https://doaj.org/article/ab0c406ad72543f9b70fd921c8e6a173
Autor:
R R Alimohammadi, M Raiesi, A Ebrahimi, S Fallah, S Kianfar, M Masoudifar, S Jamali, S Babashah, M Karimipour, R Mahdian, S Zeinali
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, Vol 2, Iss 4, Pp 5-10 (2008)
Background and Objectives Thalassaemia is one of the most common single gene disorders, which is most prevalent in the Mediterranean, the Middle East, Indian subcontinent (malaria belt). One of the mutations that result in Thalassaemia is the deletio
Externí odkaz:
https://doaj.org/article/12c90983bac54423a0c981699a657214
Autor:
E Motevasseli, M Akrami, S Zeinali, H Modaresi, AR Parsapour, K Aramesh, M Mohamadian, B Larijani
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 8, Iss 5, Pp 49-54 (2006)
Background: In recent years, new medical progresses and using modern medical technologies for diagnosis and treatment of diseases have emerged many ethical issues. One of these medical progresses is in the field of genetic researches. Genetic informa
Externí odkaz:
https://doaj.org/article/cba71987c25d46f4b57072238f373245
Autor:
S Kheradmand kia, DD Farhud, S Zeinali, AR Mowjoodi, H Najmabadi, F Pourfarzad, P Derakhshandeh
Publikováno v:
Iranian Journal of Public Health, Vol 32, Iss 3, Pp 47-53 (2003)
Duchenne Muscular Dystrophy (DMD) and the milder allelic Becker Muscular Dystrophy (BMD) are X-linked disorders. Both DMD & BMD result from heterogenous mutation in the dystrophin gene and in about 65% of the cases one or more exons of the gene are d
Externí odkaz:
https://doaj.org/article/40853bc79f5c40349dc97f0b2564b9cf
Publikováno v:
Iranian Journal of Public Health, Vol 32, Iss 3, Pp 1-6 (2003)
Hemophilia B is factor IX deficiency and is inherited as X-linked recessive disorder. The subject of carrier detection in hemophilias has received new impetus in the last several years. Analysis of factor IX gene polymorphisms is considered the best
Externí odkaz:
https://doaj.org/article/b97991e36df74ff79e22c4b3ce981640
Akademický článek
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Publikováno v:
Journal of Electronic Materials. 52:3877-3891
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::894cd0e02c9f55680cfc6698a9a9324f
https://doi.org/10.1007/s11664-023-10331-y
https://doi.org/10.1007/s11664-023-10331-y
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
International Journal of Environmental Science and Technology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdb211ad6231450976dda7a1a767de75
https://doi.org/10.1007/s13762-023-04932-7
https://doi.org/10.1007/s13762-023-04932-7
Publikováno v:
D106. HOT OFF THE PRESSES! LATE BREAKERS IN PULMONARY VASCULAR DISEASE.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0fdaaaeaf7a963a9ccabba048527b57
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a6728
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a6728