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Ethiraj Ravindran

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The Journal of Comparative Neurology|September 22, 2011
Differential expression of Brn3 transcription factors in intrinsically photosensitive retinal ganglion cells in mouseVarsha Jain, Ethiraj Ravindran, Narender K Dhingra
Annals of Human Genetics|July 30, 2019
Congenital microcephaly-linked CDK5RAP2 affects eye developmentSami Zaqout, Ethiraj Ravindran, Gisela Stoltenburg-Didinger, et al.
Frontiers in Neurology|February 27, 2023
Case report: Compound heterozygous <i>NUP85</i> variants cause autosomal recessive primary microcephalyEthiraj Ravindran, Gaetan Lesca, Louis Januel, et al.
Plos One|September 1, 2015
Novel Alternative Splice Variants of Mouse Cdk5rap2Nadine Kraemer, Lina Issa-Jahns, Gerda Neubert, et al.
Cell Cycle (Georgetown, Tex.)|May 6, 2015
Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytesNadine Kraemer, Ethiraj Ravindran, Sami Zaqout, et al.
Orphanet Journal of Rare Diseases|November 16, 2013
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutationHeba Gamal Farag, Sebastian Froehler, Konrad Oexle, et al.
Frontiers in Neurology|November 7, 2022
Case report: Expanding the phenotype of <i>ARHGEF17</i> mutations from increased intracranial aneurysm risk to a neurodevelopmental diseaseEthiraj Ravindran, Noor Ullah, Shyamala Mani, et al.
Cerebellum (London, England)|October 11, 2022
PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD PatientsSylvie Picker-Minh, Ilaria Luperi, Ethiraj Ravindran, et al.
Annals of Human Genetics|November 30, 2022
Proteome changes in autosomal recessive primary microcephalySami Zaqout, Atef Mannaa, Oliver Klein, et al.
Journal of Medical Genetics|June 1, 2021
Homozygous mutation in <i>MCM7</i> causes autosomal recessive primary microcephaly and intellectual disabilityEthiraj Ravindran, Cynthia Gutierrez de Velazco, Ali Ghazanfar, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
The Journal of Comparative Neurology|September 22, 2011
Differential expression of Brn3 transcription factors in intrinsically photosensitive retinal ganglion cells in mouseVarsha Jain, Ethiraj Ravindran, Narender K Dhingra
Annals of Human Genetics|July 30, 2019
Congenital microcephaly-linked CDK5RAP2 affects eye developmentSami Zaqout, Ethiraj Ravindran, Gisela Stoltenburg-Didinger, et al.
Frontiers in Neurology|February 27, 2023
Case report: Compound heterozygous <i>NUP85</i> variants cause autosomal recessive primary microcephalyEthiraj Ravindran, Gaetan Lesca, Louis Januel, et al.
Plos One|September 1, 2015
Novel Alternative Splice Variants of Mouse Cdk5rap2Nadine Kraemer, Lina Issa-Jahns, Gerda Neubert, et al.
Cell Cycle (Georgetown, Tex.)|May 6, 2015
Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytesNadine Kraemer, Ethiraj Ravindran, Sami Zaqout, et al.
Orphanet Journal of Rare Diseases|November 16, 2013
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutationHeba Gamal Farag, Sebastian Froehler, Konrad Oexle, et al.
Frontiers in Neurology|November 7, 2022
Case report: Expanding the phenotype of <i>ARHGEF17</i> mutations from increased intracranial aneurysm risk to a neurodevelopmental diseaseEthiraj Ravindran, Noor Ullah, Shyamala Mani, et al.
Cerebellum (London, England)|October 11, 2022
PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD PatientsSylvie Picker-Minh, Ilaria Luperi, Ethiraj Ravindran, et al.
Annals of Human Genetics|November 30, 2022
Proteome changes in autosomal recessive primary microcephalySami Zaqout, Atef Mannaa, Oliver Klein, et al.
Journal of Medical Genetics|June 1, 2021
Homozygous mutation in <i>MCM7</i> causes autosomal recessive primary microcephaly and intellectual disabilityEthiraj Ravindran, Cynthia Gutierrez de Velazco, Ali Ghazanfar, et al.
Pageof 2