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G Weber

Showing results (1141-1150 of 1,377) with videos related to

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Nature Communications|June 19, 2021
Engineering an anti-HER2 biparatopic antibody with a multimodal mechanism of actionFlorian Kast, Martin Schwill, Jakob C Stüber, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsyHenrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Acta Neuropathologica Communications|November 22, 2023
Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma familiesChristine A M Weber, Nicole Krönke, Valery Volk, et al.
Infection Control and Hospital Epidemiology|August 11, 2011
Clostridium difficile outbreak strain BI is highly endemic in Chicago area hospitalsStephanie R Black, Kingsley N Weaver, Roderick C Jones, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|March 21, 2014
Update with level 1 studies of the European Hernia Society guidelines on the treatment of inguinal hernia in adult patientsM Miserez, E Peeters, T Aufenacker, et al.
European Journal of Human Genetics : EJHG|August 2, 2020
Rare heterozygous GDF6 variants in patients with renal anomaliesHelge Martens, Imke Hennies, Maike Getwan, et al.
Annals of Neurology|October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approachesA Corrias, S Einaudi, E Chiorboli, et al.
Human Genetics|November 18, 2015
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)Anne Kosfeld, Martin Kreuzer, Christoph Daniel, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Assessment of genetic variant burden in epilepsy-associated brain lesionsLisa-Marie Niestroj, Patrick May, Mykyta Artomov, et al.
Pageof 138

Showing results (1141-1150 of 1,377) with videos related to

Sort By:
Pageof 138
Nature Communications|June 19, 2021
Engineering an anti-HER2 biparatopic antibody with a multimodal mechanism of actionFlorian Kast, Martin Schwill, Jakob C Stüber, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsyHenrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Acta Neuropathologica Communications|November 22, 2023
Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma familiesChristine A M Weber, Nicole Krönke, Valery Volk, et al.
Infection Control and Hospital Epidemiology|August 11, 2011
Clostridium difficile outbreak strain BI is highly endemic in Chicago area hospitalsStephanie R Black, Kingsley N Weaver, Roderick C Jones, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|March 21, 2014
Update with level 1 studies of the European Hernia Society guidelines on the treatment of inguinal hernia in adult patientsM Miserez, E Peeters, T Aufenacker, et al.
European Journal of Human Genetics : EJHG|August 2, 2020
Rare heterozygous GDF6 variants in patients with renal anomaliesHelge Martens, Imke Hennies, Maike Getwan, et al.
Annals of Neurology|October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approachesA Corrias, S Einaudi, E Chiorboli, et al.
Human Genetics|November 18, 2015
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)Anne Kosfeld, Martin Kreuzer, Christoph Daniel, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Assessment of genetic variant burden in epilepsy-associated brain lesionsLisa-Marie Niestroj, Patrick May, Mykyta Artomov, et al.
Pageof 138