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Bruno Reversade

Showing results (71-80 of 134) with videos related to

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Stem Cell Reports|June 8, 2017
Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem CellsJamie Trott, Ee Kim Tan, Sheena Ong, et al.
The Journal of Biological Chemistry|October 7, 2018
Human DPP9 represses NLRP1 inflammasome and protects against autoinflammatory diseases via both peptidase activity and FIIND domain bindingFranklin L Zhong, Kim Robinson, Daniel Eng Thiam Teo, et al.
Nature Genetics|February 3, 2025
Genomics of rare diseases in the Greater Middle EastIkram Chekroun, Shruti Shenbagam, Mohamed A Almarri, et al.
Cardiovascular Research|September 8, 2020
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conductionZeina R Al Sayed, Robin Canac, Bastien Cimarosti, et al.
American Journal of Human Genetics|November 26, 2019
Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary HypoplasiaAriana Kariminejad, Emmanuelle Szenker-Ravi, Caroline Lekszas, et al.
Nature Communications|January 9, 2021
Structural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8Qin Gong, Kim Robinson, Chenrui Xu, et al.
Ebiomedicine|April 15, 2016
Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?Saumya Shekhar Jamuar, Jyn Ling Kuan, Maggie Brett, et al.
The Journal of Investigative Dermatology|October 2, 2017
ENPP1 Mutation Causes Recessive Cole Disease by Altering MelanogenesisMarwa Chourabi, Mei Shan Liew, Shawn Lim, et al.
EMBO Molecular Medicine|January 18, 2023
A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencingNasrinsadat Nabavizadeh, Annkatrin Bressin, Mohammad Shboul, et al.
American Journal of Human Genetics|August 2, 2016
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 SignalingArda Cetinkaya, Jingwei Rachel Xiong, İbrahim Vargel, et al.
Pageof 14

Showing results (71-80 of 134) with videos related to

Sort By:
Pageof 14
Stem Cell Reports|June 8, 2017
Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem CellsJamie Trott, Ee Kim Tan, Sheena Ong, et al.
The Journal of Biological Chemistry|October 7, 2018
Human DPP9 represses NLRP1 inflammasome and protects against autoinflammatory diseases via both peptidase activity and FIIND domain bindingFranklin L Zhong, Kim Robinson, Daniel Eng Thiam Teo, et al.
Nature Genetics|February 3, 2025
Genomics of rare diseases in the Greater Middle EastIkram Chekroun, Shruti Shenbagam, Mohamed A Almarri, et al.
Cardiovascular Research|September 8, 2020
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conductionZeina R Al Sayed, Robin Canac, Bastien Cimarosti, et al.
American Journal of Human Genetics|November 26, 2019
Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary HypoplasiaAriana Kariminejad, Emmanuelle Szenker-Ravi, Caroline Lekszas, et al.
Nature Communications|January 9, 2021
Structural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8Qin Gong, Kim Robinson, Chenrui Xu, et al.
Ebiomedicine|April 15, 2016
Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?Saumya Shekhar Jamuar, Jyn Ling Kuan, Maggie Brett, et al.
The Journal of Investigative Dermatology|October 2, 2017
ENPP1 Mutation Causes Recessive Cole Disease by Altering MelanogenesisMarwa Chourabi, Mei Shan Liew, Shawn Lim, et al.
EMBO Molecular Medicine|January 18, 2023
A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencingNasrinsadat Nabavizadeh, Annkatrin Bressin, Mohammad Shboul, et al.
American Journal of Human Genetics|August 2, 2016
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 SignalingArda Cetinkaya, Jingwei Rachel Xiong, İbrahim Vargel, et al.
Pageof 14