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A Pandya

Showing results (141-150 of 217) with videos related to

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Toxicology Mechanisms and Methods|October 17, 2019
A multiparametric organ toxicity predictor for drug discoveryChirag N Patel, Sivakumar Prasanth Kumar, Rakesh M Rawal, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 10, 2010
Carotid stenting in asymptomatic carotid stenosis: the Calgary experienceN Shobha, M A Almekhlafi, A Pandya, et al.
American Journal of Medical Genetics|April 20, 1999
Age-related language characteristics of children and adolescents with fragile X syndromeG S Fisch, J J Holden, N J Carpenter, et al.
ACS Applied Materials & Interfaces|March 6, 2015
Silylated precision particles for controlled release of proteinsKhosrow Khodabandehlou, Amar S Kumbhar, Sohrab Habibi, et al.
Clinical Genetics|April 12, 2001
W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafnessM Tekin, K S Arnos, X J Xia, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 26, 2011
Outcomes after carotid angioplasty and stenting in symptomatic octogenariansM A Almekhlafi, P L Couillard, A Pandya, et al.
Gene|February 26, 2000
MSY2: a slowly evolving minisatellite on the human Y chromosome which provides a useful polymorphic marker in Chinese populationsW Bao, S Zhu, A Pandya, et al.
Plant Signaling & Behavior|December 5, 2019
Transcriptome-wide miRNA identification of <i>Bacopa monnieri</i>: a cross-kingdom approachHarshida Gadhavi, Maulikkumar Patel, Naman Mangukia, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 9, 2000
Validation of a multiplex methylation-sensitive PCR assay for the diagnosis of Prader-Willi and Angelman's syndromesA Buller, A Pandya, C Jackson-Cook, et al.
Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, et al.
Pageof 22

Showing results (141-150 of 217) with videos related to

Sort By:
Pageof 22
Toxicology Mechanisms and Methods|October 17, 2019
A multiparametric organ toxicity predictor for drug discoveryChirag N Patel, Sivakumar Prasanth Kumar, Rakesh M Rawal, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 10, 2010
Carotid stenting in asymptomatic carotid stenosis: the Calgary experienceN Shobha, M A Almekhlafi, A Pandya, et al.
American Journal of Medical Genetics|April 20, 1999
Age-related language characteristics of children and adolescents with fragile X syndromeG S Fisch, J J Holden, N J Carpenter, et al.
ACS Applied Materials & Interfaces|March 6, 2015
Silylated precision particles for controlled release of proteinsKhosrow Khodabandehlou, Amar S Kumbhar, Sohrab Habibi, et al.
Clinical Genetics|April 12, 2001
W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafnessM Tekin, K S Arnos, X J Xia, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 26, 2011
Outcomes after carotid angioplasty and stenting in symptomatic octogenariansM A Almekhlafi, P L Couillard, A Pandya, et al.
Gene|February 26, 2000
MSY2: a slowly evolving minisatellite on the human Y chromosome which provides a useful polymorphic marker in Chinese populationsW Bao, S Zhu, A Pandya, et al.
Plant Signaling & Behavior|December 5, 2019
Transcriptome-wide miRNA identification of <i>Bacopa monnieri</i>: a cross-kingdom approachHarshida Gadhavi, Maulikkumar Patel, Naman Mangukia, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 9, 2000
Validation of a multiplex methylation-sensitive PCR assay for the diagnosis of Prader-Willi and Angelman's syndromesA Buller, A Pandya, C Jackson-Cook, et al.
Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, et al.
Pageof 22