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Showing results (811-820 of 884) with videos related to

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Journal of Clinical Immunology|February 7, 2024
Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory DiseaseClémence David, Mihaly Badonyi, Robin Kechiche, et al.
Journal of Consulting and Clinical Psychology|May 8, 2013
Race/ethnicity, education, and treatment parameters as moderators and predictors of outcome in binge eating disorderHeather Thompson-Brenner, Debra L Franko, Douglas R Thompson, et al.
Journal of Clinical Immunology|December 12, 2017
The 2017 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Capucine Picard, et al.
Journal of Consulting and Clinical Psychology|December 29, 2011
Racial/ethnic differences in adults in randomized clinical trials of binge eating disorderDebra L Franko, Heather Thompson-Brenner, Douglas R Thompson, et al.
The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Journal of Clinical Immunology|June 7, 2022
DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signalingMaud Tusseau, Ema Lovšin, Charlotte Samaille, et al.
Journal of Clinical Immunology|August 28, 2024
Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.
Psychiatry Research|May 30, 1997
A linkage study of schizophrenia to markers within Xp11 near the MAOB geneJ Dann, L E DeLisi, M Devoto, et al.
Human Molecular Genetics|May 1, 1996
cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeatR L Margolis, O C Stine, M G McInnis, et al.
Pageof 89

Showing results (811-820 of 884) with videos related to

Sort By:
Pageof 89
Journal of Clinical Immunology|February 7, 2024
Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory DiseaseClémence David, Mihaly Badonyi, Robin Kechiche, et al.
Journal of Consulting and Clinical Psychology|May 8, 2013
Race/ethnicity, education, and treatment parameters as moderators and predictors of outcome in binge eating disorderHeather Thompson-Brenner, Debra L Franko, Douglas R Thompson, et al.
Journal of Clinical Immunology|December 12, 2017
The 2017 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Capucine Picard, et al.
Journal of Consulting and Clinical Psychology|December 29, 2011
Racial/ethnic differences in adults in randomized clinical trials of binge eating disorderDebra L Franko, Heather Thompson-Brenner, Douglas R Thompson, et al.
The Journal of Experimental Medicine|March 8, 2022
A partial form of inherited human USP18 deficiency underlies infection and inflammationMarta Martin-Fernandez, Sofija Buta, Tom Le Voyer, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Journal of Clinical Immunology|June 7, 2022
DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signalingMaud Tusseau, Ema Lovšin, Charlotte Samaille, et al.
Journal of Clinical Immunology|August 28, 2024
Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.
Psychiatry Research|May 30, 1997
A linkage study of schizophrenia to markers within Xp11 near the MAOB geneJ Dann, L E DeLisi, M Devoto, et al.
Human Molecular Genetics|May 1, 1996
cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeatR L Margolis, O C Stine, M G McInnis, et al.
Pageof 89