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Frontiers in Molecular Neuroscience
|
April 4, 2024
Structural and functional characterization of the IgSF21-neurexin2α complex and its related signaling pathways in the regulation of inhibitory synapse organization
Nicolas Chofflet, Yusuke Naito, Anthony John Pastore, et al.
Molecular Brain
|
April 15, 2017
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation
Karine Choquet, Sharon Yang, Robyn D Moir, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
September 26, 2019
Ser-Phosphorylation of PCSK9 (Proprotein Convertase Subtilisin-Kexin 9) by Fam20C (Family With Sequence Similarity 20, Member C) Kinase Enhances Its Ability to Degrade the LDLR (Low-Density Lipoprotein Receptor)
Ali Ben Djoudi Ouadda, Marie-Soleil Gauthier, Delia Susan-Resiga, et al.
Molecular and Cellular Biology
|
July 30, 2004
RPAP1, a novel human RNA polymerase II-associated protein affinity purified with recombinant wild-type and mutated polymerase subunits
Célia Jeronimo, Marie-France Langelier, Mahel Zeghouf, et al.
HGG Advances
|
January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Brain : a Journal of Neurology
|
August 28, 2023
Hypomyelination, hypodontia and craniofacial abnormalities in a Polr3b mouse model of leukodystrophy
Mackenzie A Michell-Robinson, Kristin E N Watt, Vladimir Grouza, et al.
Genes & Development
|
June 16, 2022
Recurrent chromosomal translocations in sarcomas create a megacomplex that mislocalizes NuA4/TIP60 to Polycomb target loci
Deepthi Sudarshan, Nikita Avvakumov, Marie-Eve Lalonde, et al.
American Journal of Human Genetics
|
March 27, 2018
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy
Marisa I Mendes, Mariana Gutierrez Salazar, Kether Guerrero, et al.
Clinical Biochemistry
|
January 15, 2013
Rapid development of sensitive, high-throughput, quantitative and highly selective mass spectrometric targeted immunoassays for clinically important proteins in human plasma and serum
Bryan Krastins, Amol Prakash, David A Sarracino, et al.
Nature Communications
|
July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III
Isabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
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of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
Frontiers in Molecular Neuroscience
|
April 4, 2024
Structural and functional characterization of the IgSF21-neurexin2α complex and its related signaling pathways in the regulation of inhibitory synapse organization
Nicolas Chofflet, Yusuke Naito, Anthony John Pastore, et al.
Molecular Brain
|
April 15, 2017
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation
Karine Choquet, Sharon Yang, Robyn D Moir, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
September 26, 2019
Ser-Phosphorylation of PCSK9 (Proprotein Convertase Subtilisin-Kexin 9) by Fam20C (Family With Sequence Similarity 20, Member C) Kinase Enhances Its Ability to Degrade the LDLR (Low-Density Lipoprotein Receptor)
Ali Ben Djoudi Ouadda, Marie-Soleil Gauthier, Delia Susan-Resiga, et al.
Molecular and Cellular Biology
|
July 30, 2004
RPAP1, a novel human RNA polymerase II-associated protein affinity purified with recombinant wild-type and mutated polymerase subunits
Célia Jeronimo, Marie-France Langelier, Mahel Zeghouf, et al.
HGG Advances
|
January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Brain : a Journal of Neurology
|
August 28, 2023
Hypomyelination, hypodontia and craniofacial abnormalities in a Polr3b mouse model of leukodystrophy
Mackenzie A Michell-Robinson, Kristin E N Watt, Vladimir Grouza, et al.
Genes & Development
|
June 16, 2022
Recurrent chromosomal translocations in sarcomas create a megacomplex that mislocalizes NuA4/TIP60 to Polycomb target loci
Deepthi Sudarshan, Nikita Avvakumov, Marie-Eve Lalonde, et al.
American Journal of Human Genetics
|
March 27, 2018
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy
Marisa I Mendes, Mariana Gutierrez Salazar, Kether Guerrero, et al.
Clinical Biochemistry
|
January 15, 2013
Rapid development of sensitive, high-throughput, quantitative and highly selective mass spectrometric targeted immunoassays for clinically important proteins in human plasma and serum
Bryan Krastins, Amol Prakash, David A Sarracino, et al.
Nature Communications
|
July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III
Isabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Page
of 9