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Raman Kumar

Showing results (401-410 of 429) with videos related to

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American Journal of Human Genetics|September 25, 2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityLingli Huang, Lachlan A Jolly, Saffron Willis-Owen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 5, 2024
A First-in-Human Study of Cinrebafusp Alfa, a HER2/4-1BB Bispecific Molecule, in Patients with HER2-Positive Advanced Solid MalignanciesSarina Piha-Paul, Shane A Olwill, Erika Hamilton, et al.
Human Molecular Genetics|July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiencyChuan Tan, Chloe Shard, Enzo Ranieri, et al.
Nature Medicine|May 4, 2010
Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphomaBjörn Lamprecht, Korden Walter, Stephan Kreher, et al.
Journal of Family Medicine and Primary Care|July 17, 2020
A Statement of Solidarity on COVID-19 Pandemic 2020 by the South Asian Family PhysiciansRaman Kumar, Shehla Naseem, Jayantha Jayatissa, et al.
Light, Science & Applications|December 10, 2020
Direct laser writing of volumetric gradient index lenses and waveguidesChristian R Ocier, Corey A Richards, Daniel A Bacon-Brown, et al.
Human Mutation|April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disabilityMichael J Field, Raman Kumar, Anna Hackett, et al.
Human Mutation|June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variantsDuyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Human Molecular Genetics|December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Pageof 43

Showing results (401-410 of 429) with videos related to

Sort By:
Pageof 43
American Journal of Human Genetics|September 25, 2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityLingli Huang, Lachlan A Jolly, Saffron Willis-Owen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 5, 2024
A First-in-Human Study of Cinrebafusp Alfa, a HER2/4-1BB Bispecific Molecule, in Patients with HER2-Positive Advanced Solid MalignanciesSarina Piha-Paul, Shane A Olwill, Erika Hamilton, et al.
Human Molecular Genetics|July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiencyChuan Tan, Chloe Shard, Enzo Ranieri, et al.
Nature Medicine|May 4, 2010
Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphomaBjörn Lamprecht, Korden Walter, Stephan Kreher, et al.
Journal of Family Medicine and Primary Care|July 17, 2020
A Statement of Solidarity on COVID-19 Pandemic 2020 by the South Asian Family PhysiciansRaman Kumar, Shehla Naseem, Jayantha Jayatissa, et al.
Light, Science & Applications|December 10, 2020
Direct laser writing of volumetric gradient index lenses and waveguidesChristian R Ocier, Corey A Richards, Daniel A Bacon-Brown, et al.
Human Mutation|April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disabilityMichael J Field, Raman Kumar, Anna Hackett, et al.
Human Mutation|June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variantsDuyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Human Molecular Genetics|December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Pageof 43