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T Ahmad

Showing results (171-180 of 199) with videos related to

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Medical Oncology (Northwood, London, England)|March 13, 2025
Exosomal RNAs and EZH2: unraveling the molecular dialogue driving tumor progressionAhmed Hussein Zwamel, Abdulrahman T Ahmad, Farag M A Altalbawy, et al.
Cell Death & Disease|January 19, 2013
Computational classification of mitochondrial shapes reflects stress and redox stateT Ahmad, K Aggarwal, B Pattnaik, et al.
Gut|July 17, 2003
Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31A Armuzzi, T Ahmad, K-L Ling, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|March 11, 2004
Analysis of the CC chemokine receptor 5 (CCR5) Delta32 polymorphism in Behçet's diseaseX Yang, T Ahmad, F Gogus, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 10, 2006
Pituitary enlargement in patients with primary hypothyroidismNahla M Khawaja, Bassam M Taher, Muries E Barham, et al.
European Review for Medical and Pharmacological Sciences|December 3, 2021
Knowledge and awareness levels of diabetes mellitus risk factors among nondiabetic visitors of primary health care centers: a multicenter studyH M Abdulghani, M M Ahmed, A M Al-Rezqi, et al.
Mucosal Immunology|March 6, 2009
MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel diseaseS Banerjee, B Oneda, L M Yap, et al.
Tissue Antigens|October 24, 2002
High resolution MIC genotyping: design and application to the investigation of inflammatory bowel disease susceptibilityT Ahmad, S E Marshall, K Mulcahy-Hawes, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 22, 2005
Sleepwalking associated with hyperthyroidismKamel M Ajlouni, Azmi T Ahmad, Mohamed M El-Zaheri, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2006
A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiencyA M Brooke, N F Taylor, J H Shepherd, et al.
Pageof 20

Showing results (171-180 of 199) with videos related to

Sort By:
Pageof 20
Medical Oncology (Northwood, London, England)|March 13, 2025
Exosomal RNAs and EZH2: unraveling the molecular dialogue driving tumor progressionAhmed Hussein Zwamel, Abdulrahman T Ahmad, Farag M A Altalbawy, et al.
Cell Death & Disease|January 19, 2013
Computational classification of mitochondrial shapes reflects stress and redox stateT Ahmad, K Aggarwal, B Pattnaik, et al.
Gut|July 17, 2003
Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31A Armuzzi, T Ahmad, K-L Ling, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|March 11, 2004
Analysis of the CC chemokine receptor 5 (CCR5) Delta32 polymorphism in Behçet's diseaseX Yang, T Ahmad, F Gogus, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|March 10, 2006
Pituitary enlargement in patients with primary hypothyroidismNahla M Khawaja, Bassam M Taher, Muries E Barham, et al.
European Review for Medical and Pharmacological Sciences|December 3, 2021
Knowledge and awareness levels of diabetes mellitus risk factors among nondiabetic visitors of primary health care centers: a multicenter studyH M Abdulghani, M M Ahmed, A M Al-Rezqi, et al.
Mucosal Immunology|March 6, 2009
MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel diseaseS Banerjee, B Oneda, L M Yap, et al.
Tissue Antigens|October 24, 2002
High resolution MIC genotyping: design and application to the investigation of inflammatory bowel disease susceptibilityT Ahmad, S E Marshall, K Mulcahy-Hawes, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 22, 2005
Sleepwalking associated with hyperthyroidismKamel M Ajlouni, Azmi T Ahmad, Mohamed M El-Zaheri, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2006
A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiencyA M Brooke, N F Taylor, J H Shepherd, et al.
Pageof 20