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Nature Communications
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February 7, 2017
DEK-targeting DNA aptamers as therapeutics for inflammatory arthritis
Nirit Mor-Vaknin, Anjan Saha, Maureen Legendre, et al.
PLOS Digital Health
|
June 28, 2024
Digital phenotyping correlates of mobile cognitive measures in schizophrenia: A multisite global mental health feasibility trial
Asher Cohen, Devayani Joshi, Ameya Bondre, et al.
Circulation
|
August 29, 2025
Microvascular Endothelial Cells License APS Vasculopathy Through YAP1- and CCN2-Mediated Signaling
Hui Shi, Wenying Liang, Zhixia Yang, et al.
Plos One
|
December 2, 2011
Association between Prostinogen (KLK15) genetic variants and prostate cancer risk and aggressiveness in Australia and a meta-analysis of GWAS data
Jyotsna Batra, Felicity Lose, Tracy O'Mara, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2024
Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia
Prince Jacob, Swati Singh, Gandham SriLakshmi Bhavani, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
January 16, 2024
Calprotectin Impairs Platelet Survival in Patients With Primary Antiphospholipid Syndrome
Claire K Hoy, Somanathapura K NaveenKumar, Sherwin A Navaz, et al.
Cell Reports
|
August 23, 2023
Cell-type-specific regulation of APOE and CLU levels in human neurons by the Alzheimer's disease risk gene SORL1
Hyo Lee, Aimee J Aylward, Richard V Pearse, et al.
Scientific Reports
|
April 3, 2026
Tissue resident memory T cells populate the human uveal tract
Andrew D Foers, Ian R Reekie, Lakshanie C Wickramasinghe, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders
Ankur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG
|
June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders
Ankur Chaurasia, Anju Shukla, Shruti Pande, et al.
Page
of 59
Search research articles
Search
Showing results (551-560 of 582) with videos related to
Sort By:
Page
of 59
Nature Communications
|
February 7, 2017
DEK-targeting DNA aptamers as therapeutics for inflammatory arthritis
Nirit Mor-Vaknin, Anjan Saha, Maureen Legendre, et al.
PLOS Digital Health
|
June 28, 2024
Digital phenotyping correlates of mobile cognitive measures in schizophrenia: A multisite global mental health feasibility trial
Asher Cohen, Devayani Joshi, Ameya Bondre, et al.
Circulation
|
August 29, 2025
Microvascular Endothelial Cells License APS Vasculopathy Through YAP1- and CCN2-Mediated Signaling
Hui Shi, Wenying Liang, Zhixia Yang, et al.
Plos One
|
December 2, 2011
Association between Prostinogen (KLK15) genetic variants and prostate cancer risk and aggressiveness in Australia and a meta-analysis of GWAS data
Jyotsna Batra, Felicity Lose, Tracy O'Mara, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2024
Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia
Prince Jacob, Swati Singh, Gandham SriLakshmi Bhavani, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
January 16, 2024
Calprotectin Impairs Platelet Survival in Patients With Primary Antiphospholipid Syndrome
Claire K Hoy, Somanathapura K NaveenKumar, Sherwin A Navaz, et al.
Cell Reports
|
August 23, 2023
Cell-type-specific regulation of APOE and CLU levels in human neurons by the Alzheimer's disease risk gene SORL1
Hyo Lee, Aimee J Aylward, Richard V Pearse, et al.
Scientific Reports
|
April 3, 2026
Tissue resident memory T cells populate the human uveal tract
Andrew D Foers, Ian R Reekie, Lakshanie C Wickramasinghe, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders
Ankur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG
|
June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders
Ankur Chaurasia, Anju Shukla, Shruti Pande, et al.
Page
of 59