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Rolf Stottmann

Showing results (1-10 of 8) with videos related to

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Current Protocols in Mouse Biology|February 28, 2015
ENU mutagenesis in the mouseRolf Stottmann, David Beier
Current Protocols in Human Genetics|July 22, 2014
ENU Mutagenesis in the MouseRolf Stottmann, David Beier
Developmental Biology|December 3, 2025
Challenges and opportunities for understanding the genetic causes of congenital anomaliesJanina Kueper, Ivan P Moskowitz, Rolf Stottmann, et al.
Genomics|January 19, 2010
Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sitesSavina A Jaeger, Esther T Chan, Michael F Berger, et al.
Epilepsy Research|April 9, 2026
Microtubule-stabilizing drugs suppress convulsions in a C. elegans model of CAMSAP disordersAva Schaak, Madison Walker, Braiden Worden, et al.
Development (Cambridge, England)|April 10, 2025
Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesisVicente Elorriaga, Benoît Bouloudi, Elodie Delberghe, et al.
American Journal of Medical Genetics. Part A|July 23, 2024
Long-read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalitiesKristen L Sund, Jie Liu, Joyce Lee, et al.
HGG Advances|January 20, 2022
A recurrent, <i>de novo</i> pathogenic variant in <i>ARPC4</i> disrupts actin filament formation and causes microcephaly and speech delayDianne Laboy Cintron, Alison M Muir, Abbey Scott, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Protocols in Mouse Biology|February 28, 2015
ENU mutagenesis in the mouseRolf Stottmann, David Beier
Current Protocols in Human Genetics|July 22, 2014
ENU Mutagenesis in the MouseRolf Stottmann, David Beier
Developmental Biology|December 3, 2025
Challenges and opportunities for understanding the genetic causes of congenital anomaliesJanina Kueper, Ivan P Moskowitz, Rolf Stottmann, et al.
Genomics|January 19, 2010
Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sitesSavina A Jaeger, Esther T Chan, Michael F Berger, et al.
Epilepsy Research|April 9, 2026
Microtubule-stabilizing drugs suppress convulsions in a C. elegans model of CAMSAP disordersAva Schaak, Madison Walker, Braiden Worden, et al.
Development (Cambridge, England)|April 10, 2025
Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesisVicente Elorriaga, Benoît Bouloudi, Elodie Delberghe, et al.
American Journal of Medical Genetics. Part A|July 23, 2024
Long-read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalitiesKristen L Sund, Jie Liu, Joyce Lee, et al.
HGG Advances|January 20, 2022
A recurrent, <i>de novo</i> pathogenic variant in <i>ARPC4</i> disrupts actin filament formation and causes microcephaly and speech delayDianne Laboy Cintron, Alison M Muir, Abbey Scott, et al.
Pageof 1