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Brain : a Journal of Neurology
|
March 28, 2012
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity
Gisele E Ishak, Jennifer C Dempsey, Dennis W W Shaw, et al.
Developmental Cell
|
October 5, 2021
Adaptations in Hippo-Yap signaling and myofibroblast fate underlie scar-free ear appendage wound healing in spiny mice
Chris M Brewer, Branden R Nelson, Paul Wakenight, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 10, 2026
Spatiotemporal histogenesis of the developing human cerebellum reveals dynamic layering of Bergmann glia
Guanyi He, Simon Du, Henry Tan, et al.
American Journal of Human Genetics
|
August 2, 2007
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum
Elena Boland, Jill Clayton-Smith, Victoria G Woo, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Biorxiv : the Preprint Server for Biology
|
February 8, 2024
The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner
Amanda J Stock, Pierina Gonzalez-Paredes, Luciana Previato de Almeida, et al.
Frontiers in Immunology
|
March 15, 2024
The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner
Amanda J Stock, Pierina Gonzalez Paredes, Luciana Previato de Almeida, et al.
The Journal of Clinical Investigation
|
September 25, 2014
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
Curtis R French, Sudha Seshadri, Anita L Destefano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 18, 2025
Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellum
Anders W Erickson, Henry Tan, Liam D Hendrikse, et al.
Plos Genetics
|
October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
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Search research articles
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Showing results (131-140 of 167) with videos related to
Sort By:
Page
of 17
Brain : a Journal of Neurology
|
March 28, 2012
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity
Gisele E Ishak, Jennifer C Dempsey, Dennis W W Shaw, et al.
Developmental Cell
|
October 5, 2021
Adaptations in Hippo-Yap signaling and myofibroblast fate underlie scar-free ear appendage wound healing in spiny mice
Chris M Brewer, Branden R Nelson, Paul Wakenight, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 10, 2026
Spatiotemporal histogenesis of the developing human cerebellum reveals dynamic layering of Bergmann glia
Guanyi He, Simon Du, Henry Tan, et al.
American Journal of Human Genetics
|
August 2, 2007
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum
Elena Boland, Jill Clayton-Smith, Victoria G Woo, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Biorxiv : the Preprint Server for Biology
|
February 8, 2024
The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner
Amanda J Stock, Pierina Gonzalez-Paredes, Luciana Previato de Almeida, et al.
Frontiers in Immunology
|
March 15, 2024
The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner
Amanda J Stock, Pierina Gonzalez Paredes, Luciana Previato de Almeida, et al.
The Journal of Clinical Investigation
|
September 25, 2014
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
Curtis R French, Sudha Seshadri, Anita L Destefano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 18, 2025
Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellum
Anders W Erickson, Henry Tan, Liam D Hendrikse, et al.
Plos Genetics
|
October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Page
of 17