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Robert P Erickson

Showing results (101-110 of 113) with videos related to

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Mitochondrion|November 29, 2011
Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathyMaik Hüttemann, Scott Klewer, Icksoo Lee, et al.
The American Journal of Medicine|October 17, 2021
Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration FamilyDebbie J Mustacich, Li-Wen Lai, Michael J Bernas, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with NeutropeniaCarol Clericuzio, Karine Harutyunyan, Weidong Jin, et al.
Nature Genetics|September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive developmentMax A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.
American Journal of Human Genetics|February 28, 2012
De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEPKrishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 20, 2015
Altered regulation of hepatic efflux transporters disrupts acetaminophen disposition in pediatric nonalcoholic steatohepatitisMark J Canet, Matthew D Merrell, Rhiannon N Hardwick, et al.
Journal of the National Cancer Institute|May 8, 2003
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndromeLisa L Wang, Anu Gannavarapu, Claudia A Kozinetz, et al.
Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Epilepsia|May 8, 2013
Exome sequencing reveals new causal mutations in children with epileptic encephalopathiesKrishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, et al.
Frontiers in Physiology|October 30, 2024
Cancer and lymphatic marker FOXC2 drives wound healing and fibrotic tissue formationMaia B Granoski, Katharina S Fischer, William W Hahn, et al.
Pageof 12

Showing results (101-110 of 113) with videos related to

Sort By:
Pageof 12
Mitochondrion|November 29, 2011
Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathyMaik Hüttemann, Scott Klewer, Icksoo Lee, et al.
The American Journal of Medicine|October 17, 2021
Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration FamilyDebbie J Mustacich, Li-Wen Lai, Michael J Bernas, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with NeutropeniaCarol Clericuzio, Karine Harutyunyan, Weidong Jin, et al.
Nature Genetics|September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive developmentMax A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.
American Journal of Human Genetics|February 28, 2012
De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEPKrishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 20, 2015
Altered regulation of hepatic efflux transporters disrupts acetaminophen disposition in pediatric nonalcoholic steatohepatitisMark J Canet, Matthew D Merrell, Rhiannon N Hardwick, et al.
Journal of the National Cancer Institute|May 8, 2003
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndromeLisa L Wang, Anu Gannavarapu, Claudia A Kozinetz, et al.
Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Epilepsia|May 8, 2013
Exome sequencing reveals new causal mutations in children with epileptic encephalopathiesKrishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, et al.
Frontiers in Physiology|October 30, 2024
Cancer and lymphatic marker FOXC2 drives wound healing and fibrotic tissue formationMaia B Granoski, Katharina S Fischer, William W Hahn, et al.
Pageof 12