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Soma Das

Showing results (41-50 of 186) with videos related to

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Human Mutation|January 17, 2002
Characterization of mutations in fifty North American patients with X-linked myotubular myopathyGail E Herman, Kevin Kopacz, Wei Zhao, et al.
Case Reports in Genetics|March 19, 2014
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental DisomyShaochun Bai, Anthony Lozada, Marilyn C Jones, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopiaEden V Haverfield, Amanda J Whited, Kristin S Petras, et al.
Archives of Virology|April 29, 2024
Development of an effective single-chain variable fragment recognizing a novel epitope in the hepatitis C virus E2 protein that restricts virus entry into hepatocytesSoma Das, Padmanava Behera, Dipeshwari J Shewale, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 17, 2003
Progressive dystonia in a 12-year-old boyJörg Klepper, Jörg Schaper, Gordana Raca, et al.
European Journal of Inorganic Chemistry|February 6, 2014
Water-Soluble Derivatives of Octanuclear Iron-Oxo-Pyrazolato Complexes; An Experimental and Computational StudySoma Das, Indranil Chakraborty, Dmitry Skachkov, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|October 7, 2006
Structure-toxicity analysis of type-2 alkenes: in vitro neurotoxicityRichard M Lopachin, David S Barber, Brian C Geohagen, et al.
European Journal of Human Genetics : EJHG|August 27, 2015
Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARXChing Moey, Scott Topper, Mary Karn, et al.
Brain & Development|June 4, 2013
The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencingChristopher A Tan, Scott Topper, Catherine Ward Melver, et al.
Nucleic Acids Research|December 19, 2003
THGS: a web-based database of Transmembrane Helices in Genome SequencesS A Fernando, P Selvarani, Soma Das, et al.
Pageof 19

Showing results (41-50 of 186) with videos related to

Sort By:
Pageof 19
Human Mutation|January 17, 2002
Characterization of mutations in fifty North American patients with X-linked myotubular myopathyGail E Herman, Kevin Kopacz, Wei Zhao, et al.
Case Reports in Genetics|March 19, 2014
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental DisomyShaochun Bai, Anthony Lozada, Marilyn C Jones, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopiaEden V Haverfield, Amanda J Whited, Kristin S Petras, et al.
Archives of Virology|April 29, 2024
Development of an effective single-chain variable fragment recognizing a novel epitope in the hepatitis C virus E2 protein that restricts virus entry into hepatocytesSoma Das, Padmanava Behera, Dipeshwari J Shewale, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 17, 2003
Progressive dystonia in a 12-year-old boyJörg Klepper, Jörg Schaper, Gordana Raca, et al.
European Journal of Inorganic Chemistry|February 6, 2014
Water-Soluble Derivatives of Octanuclear Iron-Oxo-Pyrazolato Complexes; An Experimental and Computational StudySoma Das, Indranil Chakraborty, Dmitry Skachkov, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|October 7, 2006
Structure-toxicity analysis of type-2 alkenes: in vitro neurotoxicityRichard M Lopachin, David S Barber, Brian C Geohagen, et al.
European Journal of Human Genetics : EJHG|August 27, 2015
Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARXChing Moey, Scott Topper, Mary Karn, et al.
Brain & Development|June 4, 2013
The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencingChristopher A Tan, Scott Topper, Catherine Ward Melver, et al.
Nucleic Acids Research|December 19, 2003
THGS: a web-based database of Transmembrane Helices in Genome SequencesS A Fernando, P Selvarani, Soma Das, et al.
Pageof 19