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H Shaikh

Showing results (191-200 of 236) with videos related to

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Brain Pathology (Zurich, Switzerland)|November 20, 2008
Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion geneAngela J Sievert, Eric M Jackson, Xiaowu Gai, et al.
Cells|June 19, 2024
Exploring Importance and Regulation of Autophagy in Cancer Stem Cells and Stem Cell-Based TherapiesMd Ataur Rahman, Ehsanul Hoque Apu, S M Rakib-Uz-Zaman, et al.
European Journal of Medical Genetics|December 23, 2008
A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delayChad R Haldeman-Englert, Xiaowu Gai, Juan Carlos Perin, et al.
Journal of Molecular Biology|March 31, 1995
Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeatsM A Batzer, C M Rubin, U Hellmann-Blumberg, et al.
BMC Cancer|November 28, 2017
Prevalence and types of high-risk human papillomaviruses in head and neck cancers from BangladeshMushfiq H Shaikh, Aminul I Khan, Anwar Sadat, et al.
Medicina (Kaunas, Lithuania)|November 27, 2024
Differences in Gender and Overall Survival for Temperature-Sensitive TP53 Mutations in Gastroesophageal CancerDanial H Shaikh, Margaret Park, Jiandong Chen, et al.
Scientific Reports|May 27, 2026
In silico DFT, ADMET and molecular docking studies of novel coumarin-linked pyrazole and quinoline derivatives as antimicrobial and antioxidant agentsNargis H Shaikh, Jay B Maheta, Darshna K Lakhnotra, et al.
Journal of Family Medicine and Primary Care|June 14, 2021
SARS CoV-2 infection in a patient with sickle cell disease - Atypical presentationAwaji Q Al-Naami, Liaqat A Khan, Faisal I Zaidan, et al.
Genome Medicine|May 10, 2023
High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencingFeyza Yilmaz, Umamaheswaran Gurusamy, Trenell J Mosley, et al.
Human Molecular Genetics|March 4, 2000
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisT H Shaikh, H Kurahashi, S C Saitta, et al.
Pageof 24

Showing results (191-200 of 236) with videos related to

Sort By:
Pageof 24
Brain Pathology (Zurich, Switzerland)|November 20, 2008
Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion geneAngela J Sievert, Eric M Jackson, Xiaowu Gai, et al.
Cells|June 19, 2024
Exploring Importance and Regulation of Autophagy in Cancer Stem Cells and Stem Cell-Based TherapiesMd Ataur Rahman, Ehsanul Hoque Apu, S M Rakib-Uz-Zaman, et al.
European Journal of Medical Genetics|December 23, 2008
A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delayChad R Haldeman-Englert, Xiaowu Gai, Juan Carlos Perin, et al.
Journal of Molecular Biology|March 31, 1995
Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeatsM A Batzer, C M Rubin, U Hellmann-Blumberg, et al.
BMC Cancer|November 28, 2017
Prevalence and types of high-risk human papillomaviruses in head and neck cancers from BangladeshMushfiq H Shaikh, Aminul I Khan, Anwar Sadat, et al.
Medicina (Kaunas, Lithuania)|November 27, 2024
Differences in Gender and Overall Survival for Temperature-Sensitive TP53 Mutations in Gastroesophageal CancerDanial H Shaikh, Margaret Park, Jiandong Chen, et al.
Scientific Reports|May 27, 2026
In silico DFT, ADMET and molecular docking studies of novel coumarin-linked pyrazole and quinoline derivatives as antimicrobial and antioxidant agentsNargis H Shaikh, Jay B Maheta, Darshna K Lakhnotra, et al.
Journal of Family Medicine and Primary Care|June 14, 2021
SARS CoV-2 infection in a patient with sickle cell disease - Atypical presentationAwaji Q Al-Naami, Liaqat A Khan, Faisal I Zaidan, et al.
Genome Medicine|May 10, 2023
High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencingFeyza Yilmaz, Umamaheswaran Gurusamy, Trenell J Mosley, et al.
Human Molecular Genetics|March 4, 2000
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysisT H Shaikh, H Kurahashi, S C Saitta, et al.
Pageof 24