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Showing results (51-60 of 65) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|February 17, 2018
PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth diseaseManisha Juneja, Abdelkrim Azmi, Jonathan Baets, et al.
The Journal of Biological Chemistry|July 1, 2011
A hypomorphic mutation in Lpin1 induces progressively improving neuropathy and lipodystrophy in the ratJoram D Mul, Karim Nadra, Noorjahan B Jagalur, et al.
The EMBO Journal|November 14, 2018
Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone-responsive myopathyTalha Rashid, Ivan Nemazanyy, Cecilia Paolini, et al.
Brain : a Journal of Neurology|June 15, 2015
Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathiesDana Safka Brozkova, Tine Deconinck, Laurie Beth Griffin, et al.
Molecular Endocrinology (Baltimore, Md.)|May 5, 2012
The glucocorticoid-induced leucine zipper (gilz/Tsc22d3-2) gene locus plays a crucial role in male fertilityPhilippe Emmanuel Suarez, Elena Gonzalez Rodriguez, Rama Soundararajan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 2, 2009
SCAP is required for timely and proper myelin membrane synthesisMark H G Verheijen, Nutabi Camargo, Valerie Verdier, et al.
Plos One|October 17, 2013
New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutationsMustafa A Salih, Emeline Mundwiller, Arif O Khan, et al.
The Journal of Biological Chemistry|April 27, 2012
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) geneDillon W Leong, Jasper C Komen, Chelsee A Hewitt, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Cell Reports|March 28, 2019
PRDM12 Is Required for Initiation of the Nociceptive Neuron Lineage during NeurogenesisLuca Bartesaghi, Yiqiao Wang, Paula Fontanet, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

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Pageof 7
Journal of Neurology, Neurosurgery, and Psychiatry|February 17, 2018
PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth diseaseManisha Juneja, Abdelkrim Azmi, Jonathan Baets, et al.
The Journal of Biological Chemistry|July 1, 2011
A hypomorphic mutation in Lpin1 induces progressively improving neuropathy and lipodystrophy in the ratJoram D Mul, Karim Nadra, Noorjahan B Jagalur, et al.
The EMBO Journal|November 14, 2018
Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone-responsive myopathyTalha Rashid, Ivan Nemazanyy, Cecilia Paolini, et al.
Brain : a Journal of Neurology|June 15, 2015
Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathiesDana Safka Brozkova, Tine Deconinck, Laurie Beth Griffin, et al.
Molecular Endocrinology (Baltimore, Md.)|May 5, 2012
The glucocorticoid-induced leucine zipper (gilz/Tsc22d3-2) gene locus plays a crucial role in male fertilityPhilippe Emmanuel Suarez, Elena Gonzalez Rodriguez, Rama Soundararajan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 2, 2009
SCAP is required for timely and proper myelin membrane synthesisMark H G Verheijen, Nutabi Camargo, Valerie Verdier, et al.
Plos One|October 17, 2013
New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutationsMustafa A Salih, Emeline Mundwiller, Arif O Khan, et al.
The Journal of Biological Chemistry|April 27, 2012
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) geneDillon W Leong, Jasper C Komen, Chelsee A Hewitt, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Cell Reports|March 28, 2019
PRDM12 Is Required for Initiation of the Nociceptive Neuron Lineage during NeurogenesisLuca Bartesaghi, Yiqiao Wang, Paula Fontanet, et al.
Pageof 7