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Manfred Boehm

Showing results (101-110 of 115) with videos related to

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Cell Host & Microbe|July 11, 2015
Flavivirus Antagonism of Type I Interferon Signaling Reveals Prolidase as a Regulator of IFNAR1 Surface ExpressionKirk J Lubick, Shelly J Robertson, Kristin L McNally, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2016
Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory diseaseQing Zhou, Xiaomin Yu, Erkan Demirkaya, et al.
Cell Stem Cell|June 6, 2024
Long-term engraftment and maturation of autologous iPSC-derived cardiomyocytes in two rhesus macaquesYongshun Lin, Noriko Sato, Sogun Hong, et al.
The Journal of Clinical Investigation|May 6, 2020
Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndromeNatalia I Dmitrieva, Avram D Walts, Dai Phuong Nguyen, et al.
Frontiers in Immunology|January 31, 2022
The Spectrum of the Deficiency of Adenosine Deaminase 2: An Observational Analysis of a 60 Patient CohortKaryl S Barron, Ivona Aksentijevich, Natalie T Deuitch, et al.
The Journal of Allergy and Clinical Immunology|November 15, 2021
TNF inhibition in vasculitis management in adenosine deaminase 2 deficiency (DADA2)Natalie T Deuitch, Dan Yang, Pui Y Lee, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
STING-STAT3-SOX18 Axis Drives EndMT and Epigenetic Reprogramming in SAVI Lung FibrosisDan Yang, Guibin Chen, Sachin Gaurav, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2021
Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published casesFrancis Rossignol, Marvid S Duarte Moreno, Jean-François Benoist, et al.
Annals of Neurology|February 12, 2014
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan AfricaModibo Sangaré, Brant Hendrickson, Hammadoun Ali Sango, et al.
Nature Genetics|December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory diseaseQing Zhou, Hongying Wang, Daniella M Schwartz, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Cell Host & Microbe|July 11, 2015
Flavivirus Antagonism of Type I Interferon Signaling Reveals Prolidase as a Regulator of IFNAR1 Surface ExpressionKirk J Lubick, Shelly J Robertson, Kristin L McNally, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2016
Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory diseaseQing Zhou, Xiaomin Yu, Erkan Demirkaya, et al.
Cell Stem Cell|June 6, 2024
Long-term engraftment and maturation of autologous iPSC-derived cardiomyocytes in two rhesus macaquesYongshun Lin, Noriko Sato, Sogun Hong, et al.
The Journal of Clinical Investigation|May 6, 2020
Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndromeNatalia I Dmitrieva, Avram D Walts, Dai Phuong Nguyen, et al.
Frontiers in Immunology|January 31, 2022
The Spectrum of the Deficiency of Adenosine Deaminase 2: An Observational Analysis of a 60 Patient CohortKaryl S Barron, Ivona Aksentijevich, Natalie T Deuitch, et al.
The Journal of Allergy and Clinical Immunology|November 15, 2021
TNF inhibition in vasculitis management in adenosine deaminase 2 deficiency (DADA2)Natalie T Deuitch, Dan Yang, Pui Y Lee, et al.
Biorxiv : the Preprint Server for Biology|April 29, 2026
STING-STAT3-SOX18 Axis Drives EndMT and Epigenetic Reprogramming in SAVI Lung FibrosisDan Yang, Guibin Chen, Sachin Gaurav, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2021
Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published casesFrancis Rossignol, Marvid S Duarte Moreno, Jean-François Benoist, et al.
Annals of Neurology|February 12, 2014
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan AfricaModibo Sangaré, Brant Hendrickson, Hammadoun Ali Sango, et al.
Nature Genetics|December 8, 2015
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory diseaseQing Zhou, Hongying Wang, Daniella M Schwartz, et al.
Pageof 12