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Graeme Clark

Showing results (11-20 of 29) with videos related to

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The Turkish Journal of Pediatrics|December 26, 2017
A pheochromocytoma case diagnosed as adrenal incidentalomaDoğuş Vurallı, Nurgün Kandemir, Graeme Clark, et al.
The Journal of Biological Chemistry|May 28, 2005
A cellular deficiency of gangliosides causes hypersensitivity to Clostridium perfringens phospholipase CMarietta Flores-Díaz, Alberto Alape-Girón, Graeme Clark, et al.
Biomaterials|September 30, 2006
The effect of polypyrrole with incorporated neurotrophin-3 on the promotion of neurite outgrowth from auditory neuronsRachael T Richardson, Brianna Thompson, Simon Moulton, et al.
European Journal of Human Genetics : EJHG|April 15, 2021
Familial wild-type gastrointestinal stromal tumour in association with germline truncating variants in both SDHA and PALB2James Whitworth, Ruth T Casey, Philip S Smith, et al.
Cancers|January 21, 2023
The Contribution of Germline Pathogenic Variants in Breast Cancer Genes to Contralateral Breast Cancer Risk in <i>BRCA1/BRCA2/PALB2</i>-Negative WomenAlexey Larionov, Eleanor Fewings, James Redman, et al.
Epigenomics|May 4, 2022
Comparison of methylation episignatures in <i>KMT2B</i>- and <i>KMT2D</i>-related human disordersSunwoo Lee, Eguzkine Ochoa, Katy Barwick, et al.
Microbiology Spectrum|February 26, 2025
Detection of mpox and other orthopoxviruses using a lateral flow device as a point-of-care diagnosticStephen M Laidlaw, David Ulaeto, Steve Lonsdale, et al.
ESMO Open|October 12, 2017
Key differences between 13 KRAS mutation detection technologies and their relevance for clinical practiceJames L Sherwood, Helen Brown, Alessandro Rettino, et al.
Human Molecular Genetics|March 24, 2022
Elongin C (ELOC/TCEB1)-associated von Hippel-Lindau diseaseAvgi Andreou, Bryndis Yngvadottir, Laia Bassaganyas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbanceEguzkine Ochoa, Sunwoo Lee, Benoit Lan-Leung, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
The Turkish Journal of Pediatrics|December 26, 2017
A pheochromocytoma case diagnosed as adrenal incidentalomaDoğuş Vurallı, Nurgün Kandemir, Graeme Clark, et al.
The Journal of Biological Chemistry|May 28, 2005
A cellular deficiency of gangliosides causes hypersensitivity to Clostridium perfringens phospholipase CMarietta Flores-Díaz, Alberto Alape-Girón, Graeme Clark, et al.
Biomaterials|September 30, 2006
The effect of polypyrrole with incorporated neurotrophin-3 on the promotion of neurite outgrowth from auditory neuronsRachael T Richardson, Brianna Thompson, Simon Moulton, et al.
European Journal of Human Genetics : EJHG|April 15, 2021
Familial wild-type gastrointestinal stromal tumour in association with germline truncating variants in both SDHA and PALB2James Whitworth, Ruth T Casey, Philip S Smith, et al.
Cancers|January 21, 2023
The Contribution of Germline Pathogenic Variants in Breast Cancer Genes to Contralateral Breast Cancer Risk in <i>BRCA1/BRCA2/PALB2</i>-Negative WomenAlexey Larionov, Eleanor Fewings, James Redman, et al.
Epigenomics|May 4, 2022
Comparison of methylation episignatures in <i>KMT2B</i>- and <i>KMT2D</i>-related human disordersSunwoo Lee, Eguzkine Ochoa, Katy Barwick, et al.
Microbiology Spectrum|February 26, 2025
Detection of mpox and other orthopoxviruses using a lateral flow device as a point-of-care diagnosticStephen M Laidlaw, David Ulaeto, Steve Lonsdale, et al.
ESMO Open|October 12, 2017
Key differences between 13 KRAS mutation detection technologies and their relevance for clinical practiceJames L Sherwood, Helen Brown, Alessandro Rettino, et al.
Human Molecular Genetics|March 24, 2022
Elongin C (ELOC/TCEB1)-associated von Hippel-Lindau diseaseAvgi Andreou, Bryndis Yngvadottir, Laia Bassaganyas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbanceEguzkine Ochoa, Sunwoo Lee, Benoit Lan-Leung, et al.
Pageof 3