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Grace Yoon

Showing results (141-150 of 177) with videos related to

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Brain : a Journal of Neurology|March 27, 2015
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxiaRebekah K Jobling, Mirna Assoum, Oleksandr Gakh, et al.
Cell|June 13, 2024
A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesisMatthew P Wilson, Takfarinas Kentache, Charlotte R Althoff, et al.
Cell|May 31, 2024
A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesisMatthew P Wilson, Takfarinas Kentache, Charlotte R Althoff, et al.
Immunity|May 31, 2025
Nociceptor neurons suppress alveolar macrophage-induced Siglec-F<sup>+</sup> neutrophil-mediated inflammation to protect against pulmonary fibrosisCarlos H Hiroki, Mortaza F Hassanabad, Manon Defaye, et al.
Brain : a Journal of Neurology|February 2, 2023
SMPD4 regulates mitotic nuclear envelope dynamics and its loss causes microcephaly and diabetesDaphne J Smits, Rachel Schot, Nathalie Krusy, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Annals of Neurology|May 31, 2017
The genetic landscape of familial congenital hydrocephalusRanad Shaheen, Mohammed Adeeb Sebai, Nisha Patel, et al.
European Journal of Human Genetics : EJHG|June 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Pageof 18

Showing results (141-150 of 177) with videos related to

Sort By:
Pageof 18
Brain : a Journal of Neurology|March 27, 2015
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxiaRebekah K Jobling, Mirna Assoum, Oleksandr Gakh, et al.
Cell|June 13, 2024
A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesisMatthew P Wilson, Takfarinas Kentache, Charlotte R Althoff, et al.
Cell|May 31, 2024
A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesisMatthew P Wilson, Takfarinas Kentache, Charlotte R Althoff, et al.
Immunity|May 31, 2025
Nociceptor neurons suppress alveolar macrophage-induced Siglec-F<sup>+</sup> neutrophil-mediated inflammation to protect against pulmonary fibrosisCarlos H Hiroki, Mortaza F Hassanabad, Manon Defaye, et al.
Brain : a Journal of Neurology|February 2, 2023
SMPD4 regulates mitotic nuclear envelope dynamics and its loss causes microcephaly and diabetesDaphne J Smits, Rachel Schot, Nathalie Krusy, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Annals of Neurology|May 31, 2017
The genetic landscape of familial congenital hydrocephalusRanad Shaheen, Mohammed Adeeb Sebai, Nisha Patel, et al.
European Journal of Human Genetics : EJHG|June 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Pageof 18