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P Erickson

Showing results (681-690 of 698) with videos related to

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Oncogene|July 22, 1998
Analysis of TEL proteins in human leukemiasH Poirel, V Lacronique, M Mauchauffé, 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.
Lymphology|November 4, 2021
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutationD J Mustacich, R I Kylat, M J Bernas, 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.
Journal of Medical Genetics|November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutationsR P Erickson, S L Dagenais, M S Caulder, 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.
Mucosal Immunology|April 13, 2019
Determinants of Tenascin-C and HIV-1 envelope binding and neutralizationRiley J Mangan, Lisa Stamper, Tomoo Ohashi, 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.
Pageof 70

Showing results (681-690 of 698) with videos related to

Sort By:
Pageof 70
Oncogene|July 22, 1998
Analysis of TEL proteins in human leukemiasH Poirel, V Lacronique, M Mauchauffé, 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.
Lymphology|November 4, 2021
Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutationD J Mustacich, R I Kylat, M J Bernas, 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.
Journal of Medical Genetics|November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutationsR P Erickson, S L Dagenais, M S Caulder, 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.
Mucosal Immunology|April 13, 2019
Determinants of Tenascin-C and HIV-1 envelope binding and neutralizationRiley J Mangan, Lisa Stamper, Tomoo Ohashi, 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.
Pageof 70