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Santasree Banerjee

Showing results (1-10 of 55) with videos related to

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Frontiers in Human Neuroscience|April 20, 2026
Editorial: Genetics and mechanisms of neurodevelopmental disordersAnjana Munshi, Ajay Kumar, Santasree Banerjee
Frontiers in Genetics|September 26, 2022
Editorial: Developmental delay and intellectual disabilitySantasree Banerjee, Anjana Munshi, Chen Li, et al.
Oncotarget|November 19, 2016
Targeted next generation sequencing identifies two novel mutations in SEPN1 in rigid spine muscular dystrophy 1Yi Dai, Shengran Liang, Yan Huang, et al.
Molecular Biosystems|July 15, 2014
In silico analysis of all point mutations on the 2B domain of K5/K14 causing epidermolysis bullosa simplex: a genotype-phenotype correlationSantasree Banerjee, Qian Wu, Ping Yu, et al.
Gene|December 21, 2024
KLHL24 associated cardiomyopathy: Gene function to clinical managementNeil Johnson, Baiyu Qi, Jianping Wen, et al.
Oncotarget|November 29, 2017
Next generation sequencing identified novel heterozygous nonsense mutation in <i>CNGB1</i> gene associated with retinitis pigmentosa in a Chinese patientSantasree Banerjee, Junping Yao, Xinxin Zhang, et al.
Frontiers in Genetics|May 8, 2018
Whole Exome Sequencing Identified a Novel Heterozygous Mutation in <i>HMBS</i> Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild AnemiaYongjiang Zheng, Jiehua Xu, Shengran Liang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 3, 2024
SEPHS1 Gene: A new master key for neurodevelopmental disordersZakaria Ahmed Mohamed, Jianli Yang, Jianping Wen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 9, 2024
Kallmann syndrome: Diagnostics and managementRajiv Kumar Yadav, Baiyu Qi, Jianping Wen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 22, 2024
The KCNB2 gene and its role in neurodevelopmental disorders: Implications for genetics and therapeutic advancesZakaria Ahmed Mohamed, Jinghua Li, Jianping Wen, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Frontiers in Human Neuroscience|April 20, 2026
Editorial: Genetics and mechanisms of neurodevelopmental disordersAnjana Munshi, Ajay Kumar, Santasree Banerjee
Frontiers in Genetics|September 26, 2022
Editorial: Developmental delay and intellectual disabilitySantasree Banerjee, Anjana Munshi, Chen Li, et al.
Oncotarget|November 19, 2016
Targeted next generation sequencing identifies two novel mutations in SEPN1 in rigid spine muscular dystrophy 1Yi Dai, Shengran Liang, Yan Huang, et al.
Molecular Biosystems|July 15, 2014
In silico analysis of all point mutations on the 2B domain of K5/K14 causing epidermolysis bullosa simplex: a genotype-phenotype correlationSantasree Banerjee, Qian Wu, Ping Yu, et al.
Gene|December 21, 2024
KLHL24 associated cardiomyopathy: Gene function to clinical managementNeil Johnson, Baiyu Qi, Jianping Wen, et al.
Oncotarget|November 29, 2017
Next generation sequencing identified novel heterozygous nonsense mutation in <i>CNGB1</i> gene associated with retinitis pigmentosa in a Chinese patientSantasree Banerjee, Junping Yao, Xinxin Zhang, et al.
Frontiers in Genetics|May 8, 2018
Whole Exome Sequencing Identified a Novel Heterozygous Mutation in <i>HMBS</i> Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild AnemiaYongjiang Zheng, Jiehua Xu, Shengran Liang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 3, 2024
SEPHS1 Gene: A new master key for neurodevelopmental disordersZakaria Ahmed Mohamed, Jianli Yang, Jianping Wen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 9, 2024
Kallmann syndrome: Diagnostics and managementRajiv Kumar Yadav, Baiyu Qi, Jianping Wen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 22, 2024
The KCNB2 gene and its role in neurodevelopmental disorders: Implications for genetics and therapeutic advancesZakaria Ahmed Mohamed, Jinghua Li, Jianping Wen, et al.
Pageof 6