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G Herrmann

Showing results (571-580 of 613) with videos related to

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European Journal of Human Genetics : EJHG|April 4, 2013
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Tracie Pennimpede, et al.
Brain : a Journal of Neurology|November 28, 2017
Synaptic phosphorylated α-synuclein in dementia with Lewy bodiesMartí Colom-Cadena, Jordi Pegueroles, Abigail G Herrmann, et al.
Journal of the American College of Cardiology|July 10, 1999
Laser angioplasty of restenosed coronary stents: results of a multicenter surveillance trial. The Laser Angioplasty of Restenosed Stents (LARS) InvestigatorsR Köster, C W Hamm, R Seabra-Gomes, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 26, 2014
Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical regionMarkus Draaken, Friederike Baudisch, Bernd Timmermann, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Cell Reports|December 12, 2019
Amyloid Beta and Tau Cooperate to Cause Reversible Behavioral and Transcriptional Deficits in a Model of Alzheimer's DiseaseEleanor K Pickett, Abigail G Herrmann, Jamie McQueen, et al.
Human Molecular Genetics|May 24, 2014
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladderHeiko Reutter, Markus Draaken, Tracie Pennimpede, et al.
Kidney International|October 25, 2013
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL associationPawaree Saisawat, Stefan Kohl, Alina C Hilger, et al.
Nature Biotechnology|March 11, 2008
Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE)Eric W Deutsch, Catherine A Ball, Jules J Berman, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Pageof 62

Showing results (571-580 of 613) with videos related to

Sort By:
Pageof 62
European Journal of Human Genetics : EJHG|April 4, 2013
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Tracie Pennimpede, et al.
Brain : a Journal of Neurology|November 28, 2017
Synaptic phosphorylated α-synuclein in dementia with Lewy bodiesMartí Colom-Cadena, Jordi Pegueroles, Abigail G Herrmann, et al.
Journal of the American College of Cardiology|July 10, 1999
Laser angioplasty of restenosed coronary stents: results of a multicenter surveillance trial. The Laser Angioplasty of Restenosed Stents (LARS) InvestigatorsR Köster, C W Hamm, R Seabra-Gomes, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 26, 2014
Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical regionMarkus Draaken, Friederike Baudisch, Bernd Timmermann, et al.
Human Genetics|June 1, 2015
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Cell Reports|December 12, 2019
Amyloid Beta and Tau Cooperate to Cause Reversible Behavioral and Transcriptional Deficits in a Model of Alzheimer's DiseaseEleanor K Pickett, Abigail G Herrmann, Jamie McQueen, et al.
Human Molecular Genetics|May 24, 2014
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladderHeiko Reutter, Markus Draaken, Tracie Pennimpede, et al.
Kidney International|October 25, 2013
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL associationPawaree Saisawat, Stefan Kohl, Alina C Hilger, et al.
Nature Biotechnology|March 11, 2008
Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE)Eric W Deutsch, Catherine A Ball, Jules J Berman, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Pageof 62