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Showing results (681-690 of 719) with videos related to

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The Journal of Allergy and Clinical Immunology|May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXASCaspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
Arthritis Care & Research|July 13, 2026
Development of a Disease Activity Index for the Assessment of VEXAS Syndrome (VEXAS-DAI)Kevin Byram, Heřman Mann, Danielle Hammond, et al.
Blood|May 24, 2022
Ruxolitinib is more effective than other JAK inhibitors to treat VEXAS syndrome: a retrospective multicenter studyMaël Heiblig, Marcela A Ferrada, Matthew J Koster, et al.
Biorxiv : the Preprint Server for Biology|June 5, 2026
Cell autonomous inflammation in VEXAS is mediated by cGAS-STINGSamuel J Magaziner, Jason C Collins, Brecca Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2023
Germline <i>C1GALT1C1</i> mutation causes a multisystem chaperonopathyFlorian Erger, Rajindra P Aryal, Björn Reusch, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2024
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tractMarcin Kołbuc, Mateusz F Kołek, Rafał Motyka, et al.
Kidney International Reports|October 27, 2025
Novel <i>RRAGD</i> Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, François Jouret, Leire Madariaga, et al.
Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
Kidney International Reports|October 18, 2023
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria ConsortiumElisabeth L Metry, Sander F Garrelfs, Lisa J Deesker, et al.
Journal of the American Society of Nephrology : JASN|July 4, 2018
Noninvasive Immunohistochemical Diagnosis and Novel <i>MUC1</i> Mutations Causing Autosomal Dominant Tubulointerstitial Kidney DiseaseMartina Živná, Kendrah Kidd, Anna Přistoupilová, et al.
Pageof 72

Showing results (681-690 of 719) with videos related to

Sort By:
Pageof 72
The Journal of Allergy and Clinical Immunology|May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXASCaspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
Arthritis Care & Research|July 13, 2026
Development of a Disease Activity Index for the Assessment of VEXAS Syndrome (VEXAS-DAI)Kevin Byram, Heřman Mann, Danielle Hammond, et al.
Blood|May 24, 2022
Ruxolitinib is more effective than other JAK inhibitors to treat VEXAS syndrome: a retrospective multicenter studyMaël Heiblig, Marcela A Ferrada, Matthew J Koster, et al.
Biorxiv : the Preprint Server for Biology|June 5, 2026
Cell autonomous inflammation in VEXAS is mediated by cGAS-STINGSamuel J Magaziner, Jason C Collins, Brecca Miller, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2023
Germline <i>C1GALT1C1</i> mutation causes a multisystem chaperonopathyFlorian Erger, Rajindra P Aryal, Björn Reusch, et al.
Pediatric Nephrology (Berlin, Germany)|January 10, 2024
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tractMarcin Kołbuc, Mateusz F Kołek, Rafał Motyka, et al.
Kidney International Reports|October 27, 2025
Novel <i>RRAGD</i> Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, François Jouret, Leire Madariaga, et al.
Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
Kidney International Reports|October 18, 2023
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria ConsortiumElisabeth L Metry, Sander F Garrelfs, Lisa J Deesker, et al.
Journal of the American Society of Nephrology : JASN|July 4, 2018
Noninvasive Immunohistochemical Diagnosis and Novel <i>MUC1</i> Mutations Causing Autosomal Dominant Tubulointerstitial Kidney DiseaseMartina Živná, Kendrah Kidd, Anna Přistoupilová, et al.
Pageof 72