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Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
December 19, 2013
Tbx4 interacts with the short stature homeobox gene Shox2 in limb development
Anne Glaser, Ripla Arora, Sandra Hoffmann, et al.
Stem Cell Research
|
December 17, 2017
Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathways
Stefanie Schmitteckert, Anne Griesbeck, Simon Sumer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 2022
Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome
Jing Wang, Henning Fröhlich, Felipe Bodaleo Torres, et al.
Human Genetics
|
April 10, 2002
Molecular characterization of a ring X chromosome in a male with short stature
Jay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
Genes
|
December 24, 2021
Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism
Philipp Vick, Birgit Eberle, Daniela Choukair, et al.
British Journal of Haematology
|
April 16, 2003
Pseudoautosomal linkage of familial Hodgkin's lymphoma: molecular analysis of a unique family with Leri-Weill dyschondrosteosis and Hodgkins lymphoma
Deborah J Shears, Volker Endris, David A Gokhale, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
June 26, 2025
Inhibition of Phosphodiesterase 10A by MP-10 Rescues Behavioral Deficits and Normalizes Microglial Morphology and Synaptic Pruning in A Mouse Model of FOXP1 Syndrome
Henning Fröhlich, Jing Wang, Ferdinand Althammer, et al.
Stem Cell Research
|
April 9, 2017
Comparative expression analysis of Shox2-deficient embryonic stem cell-derived sinoatrial node-like cells
Sandra Hoffmann, Stefanie Schmitteckert, Anne Griesbeck, et al.
Plos One
|
May 27, 2015
Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortex
Xue Li, Jian Xiao, Henning Fröhlich, et al.
Journal of Medical Genetics
|
November 15, 2015
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family
Rafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, et al.
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Search research articles
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Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
December 19, 2013
Tbx4 interacts with the short stature homeobox gene Shox2 in limb development
Anne Glaser, Ripla Arora, Sandra Hoffmann, et al.
Stem Cell Research
|
December 17, 2017
Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathways
Stefanie Schmitteckert, Anne Griesbeck, Simon Sumer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 2022
Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome
Jing Wang, Henning Fröhlich, Felipe Bodaleo Torres, et al.
Human Genetics
|
April 10, 2002
Molecular characterization of a ring X chromosome in a male with short stature
Jay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
Genes
|
December 24, 2021
Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism
Philipp Vick, Birgit Eberle, Daniela Choukair, et al.
British Journal of Haematology
|
April 16, 2003
Pseudoautosomal linkage of familial Hodgkin's lymphoma: molecular analysis of a unique family with Leri-Weill dyschondrosteosis and Hodgkins lymphoma
Deborah J Shears, Volker Endris, David A Gokhale, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
June 26, 2025
Inhibition of Phosphodiesterase 10A by MP-10 Rescues Behavioral Deficits and Normalizes Microglial Morphology and Synaptic Pruning in A Mouse Model of FOXP1 Syndrome
Henning Fröhlich, Jing Wang, Ferdinand Althammer, et al.
Stem Cell Research
|
April 9, 2017
Comparative expression analysis of Shox2-deficient embryonic stem cell-derived sinoatrial node-like cells
Sandra Hoffmann, Stefanie Schmitteckert, Anne Griesbeck, et al.
Plos One
|
May 27, 2015
Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortex
Xue Li, Jian Xiao, Henning Fröhlich, et al.
Journal of Medical Genetics
|
November 15, 2015
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family
Rafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, et al.
Page
of 8