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W Ahmad

Showing results (101-110 of 193) with videos related to

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Genetics and Molecular Research : GMR|July 16, 2016
HVSI polymorphism indicates multiple origins of mtDNA in the Hazarewal population of Northern PakistanN Akbar, H Ahmad, M S Nadeem, et al.
Molecular and Cellular Biochemistry|February 12, 2015
The BM2 protein of influenza B virus interacts with p53 and inhibits its transcriptional and apoptotic activitiesH Zhang, H Yu, J Wang, et al.
Journal of Medical Genetics|November 3, 2004
A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3M Aslam, M H Chahrour, A Razzaq, et al.
Annals of Human Genetics|April 25, 2007
Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2A Wali, G Ali, P John, et al.
Clinical Genetics|June 28, 2007
Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32A Wali, M S Chishti, M Ayub, et al.
The British Journal of Dermatology|September 30, 2016
Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbingK Shah, T M Ferrara, A Jan, et al.
Cureus|November 4, 2024
Translation, Cultural Adaptation, and Validation of the Arab Version of the Adolescent Food Parenting Questionnaire (AFPQ) in Kut City, IraqAbbas Ali Alkinani, A J Rohana, Ruhaya Hasan, et al.
Cureus|November 18, 2024
Translation and Validation of a Culturally Adapted Arabic Version of the Beverage Intake Questionnaire (BEVQ)Abbas A Alkinani, A J Rohana, Ruhaya Hasan, et al.
Experimental Dermatology|March 22, 2001
Characterization of the desmosomal cadherin gene family: genomic organization of two desmoglein genes on human chromosome 18q12J Frank, P B Cserhalmi-Friedman, W Ahmad, et al.
The British Journal of Dermatology|April 11, 2016
The angiotensin-converting enzyme gene insertion polymorphism: a higher risk for psoriasis in male patientsS Munir, S B Rahman, S Rehman, et al.
Pageof 20

Showing results (101-110 of 193) with videos related to

Sort By:
Pageof 20
Genetics and Molecular Research : GMR|July 16, 2016
HVSI polymorphism indicates multiple origins of mtDNA in the Hazarewal population of Northern PakistanN Akbar, H Ahmad, M S Nadeem, et al.
Molecular and Cellular Biochemistry|February 12, 2015
The BM2 protein of influenza B virus interacts with p53 and inhibits its transcriptional and apoptotic activitiesH Zhang, H Yu, J Wang, et al.
Journal of Medical Genetics|November 3, 2004
A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3M Aslam, M H Chahrour, A Razzaq, et al.
Annals of Human Genetics|April 25, 2007
Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2A Wali, G Ali, P John, et al.
Clinical Genetics|June 28, 2007
Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32A Wali, M S Chishti, M Ayub, et al.
The British Journal of Dermatology|September 30, 2016
Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbingK Shah, T M Ferrara, A Jan, et al.
Cureus|November 4, 2024
Translation, Cultural Adaptation, and Validation of the Arab Version of the Adolescent Food Parenting Questionnaire (AFPQ) in Kut City, IraqAbbas Ali Alkinani, A J Rohana, Ruhaya Hasan, et al.
Cureus|November 18, 2024
Translation and Validation of a Culturally Adapted Arabic Version of the Beverage Intake Questionnaire (BEVQ)Abbas A Alkinani, A J Rohana, Ruhaya Hasan, et al.
Experimental Dermatology|March 22, 2001
Characterization of the desmosomal cadherin gene family: genomic organization of two desmoglein genes on human chromosome 18q12J Frank, P B Cserhalmi-Friedman, W Ahmad, et al.
The British Journal of Dermatology|April 11, 2016
The angiotensin-converting enzyme gene insertion polymorphism: a higher risk for psoriasis in male patientsS Munir, S B Rahman, S Rehman, et al.
Pageof 20