Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Abbas Parsian"'
Autor:
Zohreh Rahimi, Abbas Parsian
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 3, Iss 1, Pp e2011024-e2011024 (2011)
Hemoglobin S in homozygous state or in combination with one of the structural variants of Hb D-Punjab, Hb O-Arab, Hb C or β-thalassemia mutation results in sickle cell disease (SCD) that is characterized by chronic hemolytic anemia and tissue injury
Externí odkaz:
https://doaj.org/article/79cb18a243624a658ebc236a7da71547
Autor:
Veronica Wilson, Bridget F. Grant, Tulshi D. Saha, Amy Z. Fan, Abbas Parsian, David Goldman, Colin A. Hodgkinson, S. Patricia Chou, Haitao Zhang, W. June Ruan, Bradley T. Kerridge, Boji Huang, Jeesun Jung
Publikováno v:
Mol Psychiatry
Substance use disorders (SUDs) are moderately to highly heritable and are in part cross-transmitted genetically, as observed in twin and family studies. We performed exome-focused genotyping to examine the cross-transmission of four SUDs: alcohol use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7318652b1d68041b00709a091f83365a
https://doi.org/10.1038/s41380-021-01370-0
https://doi.org/10.1038/s41380-021-01370-0
Autor:
Abbas Parsian, John I. Nurnberger
Publikováno v:
European Neuropsychopharmacology. 29:S730-S731
Overall Abstract Genome-wide association studies (GWAS) of alcoholism and other substance use disorders have led to the discovery of variants associated with alcohol drinking, tobacco smoking, opioid use, and a host of other related traits. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd0079ba286d5929dffc4132fb38a808
https://doi.org/10.1016/j.euroneuro.2017.06.053
https://doi.org/10.1016/j.euroneuro.2017.06.053
Publikováno v:
Journal of Thrombosis and Thrombolysis. 33:109-115
The aim of the present study was to investigate the frequency and the possible association between thrombophilic mutations of factor V Leiden (FVL) and prothrombin G20210A with preeclampsia among Kurdish population of Western Iran. We studied 198 wom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57c96e98a814f631709ce39bf7e7ed30
https://doi.org/10.1007/s11239-011-0653-y
https://doi.org/10.1007/s11239-011-0653-y
Autor:
Zohreh Rahimi, Ziba Rahimi, Zainab Ahmadian, Asad Vaisi-Raygani, Abbas Parsian, Reza Akramipour
Publikováno v:
Molecular Biology Reports. 39:2195-2200
In order to determine the influence of polymorphism in thymidylate synthase (TS 28-bp repeat) and methionine synthase (MS A2756G) genes on the susceptibility to acute lymphoblastic leukemia (ALL), 73 children with ALL and 128 age and sex matched unre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::005dc6cdeffbc08cbcea02b927fb7b28
https://doi.org/10.1007/s11033-011-0968-y
https://doi.org/10.1007/s11033-011-0968-y
Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden
Autor:
Ardeshir Ghavamzadeh, Ali Shahriari-Ahmadi, Zohreh Rahimi, Kamran Mansouri, Kamran Alimogaddam, Abbas Parsian, Mozafar Aznab, Mansour Rezaei, Hadi Mozafari
Publikováno v:
Blood Coagulation & Fibrinolysis. 21:385-388
The aim of present study was to investigate the prevalence of factor V Leiden (FVL) c.1691G>A, prothrombin g.20210G>A and methylenetetrahydrofolate reductase (MTHFR) c.677C>T in deep vein thrombosis (DVT) patients and their possible association with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0718c49e873f906d55f9dd9aa237f547
https://doi.org/10.1097/mbc.0b013e328330e69a
https://doi.org/10.1097/mbc.0b013e328330e69a
Publikováno v:
Molecular Biology Reports. 37:149-154
Beta Thalassemia has been reported to be a common genetic disorder in Iran. To establish the molecular spectrum of the beta thalassemias in the Kermanshah Province of Iran, 185 unrelated beta thalassemia patients with Kurdish ethnic background were s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad40bf70de26098ba2d9ae21f66d42eb
https://doi.org/10.1007/s11033-009-9560-0
https://doi.org/10.1007/s11033-009-9560-0
Publikováno v:
Behavioural Brain Research. 177:37-44
Ethanol associated addictive behaviors are governed by a combination of multiple gene action (polygenic or quantitative trait) and environmental factors. We produced F2 progeny from F1 crosses derived from the alcohol-preferring Fawn-Hooded (FH/Wjd)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e22db4520494713c39470dbd70825459
https://doi.org/10.1016/j.bbr.2006.11.008
https://doi.org/10.1016/j.bbr.2006.11.008
Publikováno v:
Neuroscience & Biobehavioral Reviews. 31:103-114
This review will consider the evidence supporting the view that a specific substrain of Fawn-Hooded rat (FH/Wjd) exhibits co-occurring depressive-like behavior and high alcohol intake independently. First, the FH/Wjd rat is compared with other Fawn-H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6760192b74076c316c0a1b2a44764b
https://doi.org/10.1016/j.neubiorev.2006.07.002
https://doi.org/10.1016/j.neubiorev.2006.07.002
Autor:
Margery H. Mark, P. Vieregge, Ravi Prakash, David J. Burn, Irene Litvan, J. E. Tobin, Patrick F. Chinnery, Mark F. Lew, Christine Klein, Anita L. DeStefano, Marie Saint-Hilaire, Richard H. Myers, Garth A. Nicholson, JT Slevin, Peter P. Pramstaller, Mark Guttman, Mei Sun, Stefano Goldwurm, Lawrence I. Golbe, Abbas Parsian, Holly A. Shill, S. Williamson, Brad A. Racette, G. F. Wooten, CJ Berg, Kenneth B. Baker, James F. Gusella, Oksana Suchowersky, Carlos Singer, Jeanne C. Latourelle, M. L. Giroux, Marcy E. MacDonald, Gianni Pezzoli, Ray L. Watts, John H. Growdon, Franca Cambi, Jemma B. Wilk, Joel S. Perlmutter
Publikováno v:
Neurology. 67:2206-2210
Background: Polymorphisms in the glutathione S-transferase pi gene ( GSTP1 ), encoding GSTP1-1, a detoxification enzyme, may increase the risk of Parkinson disease (PD) with exposure to pesticides. Using the Gene PD Study sample of familial PD cases,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4284eb5cc990061e837eac092db7e37c
https://doi.org/10.1212/01.wnl.0000249149.22407.d1
https://doi.org/10.1212/01.wnl.0000249149.22407.d1