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M Barmada

Showing results (21-30 of 43) with videos related to

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Autoimmune Diseases|March 20, 2013
Genome-wide association study of antiphospholipid antibodiesM Ilyas Kamboh, Xingbin Wang, Amy H Kao, et al.
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Translational Psychiatry|June 3, 2015
Genome-wide copy-number variation study of psychosis in Alzheimer's diseaseX Zheng, F Y Demirci, M M Barmada, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 25, 2005
The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USAA Schneider, E C Lawrence, M M Barmada, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Replication study of genome-wide associated SNPs with late-onset Alzheimer's diseaseL C Burns, R L Minster, F Y Demirci, et al.
Journal of Alzheimer'S Disease : JAD|August 13, 2014
Genetic determinants of disease progression in Alzheimer's diseaseXingbin Wang, Oscar L Lopez, Robert A Sweet, et al.
Journal of Alzheimer'S Disease : JAD|February 5, 2015
Genetic Determinants of Survival in Patientswith Alzheimer’s DiseaseXingbin Wang, Oscar Lopez, Robert A Sweet, et al.
Cannabis and Cannabinoid Research|February 23, 2024
Acute Effects of Monoacylglycerol Lipase Inhibitor ABX1431 on Neuronal Hyperexcitability, Nociception, Locomotion, and the Endocannabinoid System in HIV-1 Tat Male MiceBarkha J Yadav-Samudrala, Havilah P Ravula, Karenna M Barmada, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Autoimmune Diseases|March 20, 2013
Genome-wide association study of antiphospholipid antibodiesM Ilyas Kamboh, Xingbin Wang, Amy H Kao, et al.
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Translational Psychiatry|June 3, 2015
Genome-wide copy-number variation study of psychosis in Alzheimer's diseaseX Zheng, F Y Demirci, M M Barmada, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|May 25, 2005
The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USAA Schneider, E C Lawrence, M M Barmada, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Replication study of genome-wide associated SNPs with late-onset Alzheimer's diseaseL C Burns, R L Minster, F Y Demirci, et al.
Journal of Alzheimer'S Disease : JAD|August 13, 2014
Genetic determinants of disease progression in Alzheimer's diseaseXingbin Wang, Oscar L Lopez, Robert A Sweet, et al.
Journal of Alzheimer'S Disease : JAD|February 5, 2015
Genetic Determinants of Survival in Patientswith Alzheimer’s DiseaseXingbin Wang, Oscar Lopez, Robert A Sweet, et al.
Cannabis and Cannabinoid Research|February 23, 2024
Acute Effects of Monoacylglycerol Lipase Inhibitor ABX1431 on Neuronal Hyperexcitability, Nociception, Locomotion, and the Endocannabinoid System in HIV-1 Tat Male MiceBarkha J Yadav-Samudrala, Havilah P Ravula, Karenna M Barmada, et al.
Journal of Medical Genetics|December 10, 2002
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathyT C Hart, M C Gorry, P S Hart, et al.
Pageof 5