H H Göring - JoVE Visualize

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Laboratory Investigation; a Journal of Technical Methods and Pathology|March 16, 2002

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscleJohn J Bissler, Monica Tsoras, Harald H H Göring, et al.

Human Molecular Genetics|May 30, 2015

Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variantsJubao Duan, Alan R Sanders, Winton Moy, et al.

Radiology|February 26, 2003

Radiologic phenotypes in lumbar MR imaging for a gene defect in the COL9A3 gene of type IX collagenJaro Karppinen, Eija Pääkkö, Petteri Paassilta, et al.

Atherosclerosis|November 23, 2006

Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican AmericansJack W Kent, Michael C Mahaney, Anthony G Comuzzie, et al.

Diabetes/Metabolism Research and Reviews|January 31, 2006

A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American familyDonna M Lehman, Jeanette Hamlington, Kelly J Hunt, et al.

European Journal of Human Genetics : EJHG|January 31, 2020

Genotype phasing in pedigrees using whole-genome sequence dataAugust N Blackburn, Lucy Blondell, Mark Z Kos, et al.

Pediatric Research|August 2, 2007

Genome-wide scan for serum ghrelin detects linkage on chromosome 1p36 in Hispanic children: results from the Viva La Familia studyV Saroja Voruganti, Harald H H Göring, Vincent P Diego, et al.

Cancer Chemotherapy and Pharmacology|February 20, 2013

Genetic basis for the increased expression of vacuolar H+ translocating ATPase genes upon imatinib treatment in human lymphoblastoid cellsHemant Kulkarni, Harald H H Göring, Joanne E Curran, et al.

Cerebral Cortex (New York, N.Y. : 1991)|December 1, 2017

Human Cortical Thickness Organized into Genetically-determined Communities across Spatial ResolutionsAaron F Alexander-Bloch, Samuel R Mathias, Peter T Fox, et al.

Osteoarthritis and Cartilage|June 1, 2005

The role of sequence variations within the genes encoding collagen II, IX and XI in non-syndromic, early-onset osteoarthritisE Jakkula, M Melkoniemi, I Kiviranta, et al.

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Showing results (41-50 of 152) with videos related to

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Pageof 16

Laboratory Investigation; a Journal of Technical Methods and Pathology|March 16, 2002

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscleJohn J Bissler, Monica Tsoras, Harald H H Göring, et al.

Human Molecular Genetics|May 30, 2015

Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variantsJubao Duan, Alan R Sanders, Winton Moy, et al.

Radiology|February 26, 2003

Radiologic phenotypes in lumbar MR imaging for a gene defect in the COL9A3 gene of type IX collagenJaro Karppinen, Eija Pääkkö, Petteri Paassilta, et al.

Atherosclerosis|November 23, 2006

Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican AmericansJack W Kent, Michael C Mahaney, Anthony G Comuzzie, et al.

Diabetes/Metabolism Research and Reviews|January 31, 2006

A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American familyDonna M Lehman, Jeanette Hamlington, Kelly J Hunt, et al.

European Journal of Human Genetics : EJHG|January 31, 2020

Genotype phasing in pedigrees using whole-genome sequence dataAugust N Blackburn, Lucy Blondell, Mark Z Kos, et al.

Pediatric Research|August 2, 2007

Genome-wide scan for serum ghrelin detects linkage on chromosome 1p36 in Hispanic children: results from the Viva La Familia studyV Saroja Voruganti, Harald H H Göring, Vincent P Diego, et al.

Cancer Chemotherapy and Pharmacology|February 20, 2013

Genetic basis for the increased expression of vacuolar H+ translocating ATPase genes upon imatinib treatment in human lymphoblastoid cellsHemant Kulkarni, Harald H H Göring, Joanne E Curran, et al.

Cerebral Cortex (New York, N.Y. : 1991)|December 1, 2017

Human Cortical Thickness Organized into Genetically-determined Communities across Spatial ResolutionsAaron F Alexander-Bloch, Samuel R Mathias, Peter T Fox, et al.

Osteoarthritis and Cartilage|June 1, 2005

The role of sequence variations within the genes encoding collagen II, IX and XI in non-syndromic, early-onset osteoarthritisE Jakkula, M Melkoniemi, I Kiviranta, et al.

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