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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Functional variation in promoter region of monoamine oxidase A and subtypes of alcoholism: haplotype analysisAbbas Parsian, C Robert Cloninger, Rashmi Sinha, et al.Clinical Biochemistry|October 30, 2012
MTHFR C677T and eNOS G894T variants in preeclamptic women: Contribution to lipid peroxidation and oxidative stressZohreh Rahimi, Shohreh Malek-Khosravi, Ziba Rahimi, et al.Journal of Thrombosis and Thrombolysis|November 10, 2011
Thrombophilic mutations and susceptibility to preeclampsia in Western IranShohreh Malek-Khosravi, Zohreh Rahimi, Ziba Rahimi, et al.Parkinsonism & Related Disorders|May 4, 2004
Association of a variation in the promoter region of the brain-derived neurotrophic factor gene with familial Parkinson's diseaseAbbas Parsian, Rashmi Sinha, Brad Racette, et al.Behavioural Brain Research|December 13, 2006
Analysis of alcohol-related phenotypes in F2 progeny derived from FH/Wjd and ACI/N rat strains reveals independent measures and sex differencesBiswanath Patra, David H Overstreet, Amir H Rezvani, et al.Neuroscience and Biobehavioral Reviews|September 20, 2006
Depressive-like behavior and high alcohol drinking co-occur in the FH/WJD rat but appear to be under independent genetic controlDavid H Overstreet, Amir H Rezvani, Elvan Djouma, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 9, 2013
Butyrylcholinesterase (BChE) activity is associated with the risk of preeclampsia: influence on lipid and lipoprotein metabolism and oxidative stressZohreh Rahimi, Reza Ahmadi, Asad Vaisi-Raygani, et al.Molecular Biology Reports|June 7, 2011
Thymidylate synthase and methionine synthase polymorphisms are not associated with susceptibility to childhood acute lymphoblastic leukemia in Kurdish population from Western IranZohreh Rahimi, Zainab Ahmadian, Reza Akramipour, et al.Blood Cells, Molecules & Diseases|January 15, 2009
Haplotype analysis of beta thalassemia patients in Western IranZohreh Rahimi, Adriana Muniz, Reza Akramipour, et al.Parkinsonism & Related Disorders|August 30, 2008
LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson's diseaseBiswanath Patra, Azemat J Parsian, Brad A Racette, et al.Pageof 3