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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 18, 2022
DNA methylation episignature for Witteveen-Kolk syndrome due to SIN3A haploinsufficiency
Jet Coenen-van der Spek, Raissa Relator, Jennifer Kerkhof, et al.
Plos One
|
October 24, 2024
Impact of variable titer COVID-19 convalescent plasma and recipient SARS-CoV2-specific humoral immunity on survival in hospitalized patients
Carlo J Iasella, Stefanie J Hannan, Emily J Lyons, et al.
Neurobiology of Aging
|
November 17, 2021
Paradoxical cognitive trajectories in men from earlier to later adulthood
Graham M L Eglit, Jeremy A Elman, Mathew S Panizzon, et al.
Brain Communications
|
August 16, 2021
12-year prediction of mild cognitive impairment aided by Alzheimer's brain signatures at mean age 56
McKenna E Williams, Jeremy A Elman, Linda K McEvoy, et al.
AJNR. American Journal of Neuroradiology
|
June 30, 2022
Brain Abnormalities in Patients with Germline Variants in <i>H3F3</i>: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors
C A P F Alves, O Sherbini, F D'Arco, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
June 24, 2021
Selecting the Right Criteria and Proper Classification to Diagnose Mast Cell Activation Syndromes: A Critical Review
Theo Gülen, Cem Akin, Patrizia Bonadonna, et al.
Communications Biology
|
September 9, 2024
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
Shahzad Ahmad, Mohammad Aslam Imtiaz, Aniket Mishra, et al.
European Journal of Medical Genetics
|
November 22, 2022
Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway
Julian Delanne, Magaly Lecat, Patrick R Blackburn, et al.
Cell Systems
|
April 16, 2018
A Library of Phosphoproteomic and Chromatin Signatures for Characterizing Cellular Responses to Drug Perturbations
Lev Litichevskiy, Ryan Peckner, Jennifer G Abelin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 19, 2025
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic disease
Mehul Sharma, Simran Samra, Yihui Liu, et al.
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of 125
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Showing results (1171-1180 of 1,244) with videos related to
Sort By:
Page
of 125
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 18, 2022
DNA methylation episignature for Witteveen-Kolk syndrome due to SIN3A haploinsufficiency
Jet Coenen-van der Spek, Raissa Relator, Jennifer Kerkhof, et al.
Plos One
|
October 24, 2024
Impact of variable titer COVID-19 convalescent plasma and recipient SARS-CoV2-specific humoral immunity on survival in hospitalized patients
Carlo J Iasella, Stefanie J Hannan, Emily J Lyons, et al.
Neurobiology of Aging
|
November 17, 2021
Paradoxical cognitive trajectories in men from earlier to later adulthood
Graham M L Eglit, Jeremy A Elman, Mathew S Panizzon, et al.
Brain Communications
|
August 16, 2021
12-year prediction of mild cognitive impairment aided by Alzheimer's brain signatures at mean age 56
McKenna E Williams, Jeremy A Elman, Linda K McEvoy, et al.
AJNR. American Journal of Neuroradiology
|
June 30, 2022
Brain Abnormalities in Patients with Germline Variants in <i>H3F3</i>: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors
C A P F Alves, O Sherbini, F D'Arco, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
June 24, 2021
Selecting the Right Criteria and Proper Classification to Diagnose Mast Cell Activation Syndromes: A Critical Review
Theo Gülen, Cem Akin, Patrizia Bonadonna, et al.
Communications Biology
|
September 9, 2024
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
Shahzad Ahmad, Mohammad Aslam Imtiaz, Aniket Mishra, et al.
European Journal of Medical Genetics
|
November 22, 2022
Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway
Julian Delanne, Magaly Lecat, Patrick R Blackburn, et al.
Cell Systems
|
April 16, 2018
A Library of Phosphoproteomic and Chromatin Signatures for Characterizing Cellular Responses to Drug Perturbations
Lev Litichevskiy, Ryan Peckner, Jennifer G Abelin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 19, 2025
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic disease
Mehul Sharma, Simran Samra, Yihui Liu, et al.
Page
of 125