Search research articles
Contact Us
Filters
Showing results (261-270 of 271) with videos related to
Page
of 28
Sort By:
European Journal of Human Genetics : EJHG
|
July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Mythily Ganapathi, Leticia S Matsuoka, Michael March, et al.
Journal of the American Heart Association
|
August 5, 2021
Rheumatic Heart Disease in the United States: Forgotten But Not Gone: Results of a 10 Year Multicenter Review
Sarah R de Loizaga, Lindsay Arthur, Bhawna Arya, et al.
Nature Communications
|
April 8, 2023
Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer
Mary C Bedard, Tafadzwa Chihanga, Adrean Carlile, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 16, 2016
Official American Thoracic Society/Japanese Respiratory Society Clinical Practice Guidelines: Lymphangioleiomyomatosis Diagnosis and Management
Francis X McCormack, Nishant Gupta, Geraldine R Finlay, et al.
Developmental Cell
|
December 22, 2021
A census of the lung: CellCards from LungMAP
Xin Sun, Anne-Karina Perl, Rongbo Li, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
June 11, 2026
International Society for Heart and Lung Transplantation Scientific Statement on pulmonary antibody-mediated rejection and proposed graft, antibody, and pathology (GAP) definition
Fiorella Calabrese, Deborah J Levine, Benjamin A Adam, et al.
Pediatric Blood & Cancer
|
July 22, 2025
High Prevalence of Abnormal Baseline Lung Function in Pediatric and Young Adult Hematopoietic Stem Cell Transplant Recipients: A Report from the TRANSPIRE Study
Jane Koo, Richard Cooper, Stephanie L Edwards, et al.
Annals of Neurology
|
August 22, 2023
GABRA1-Related Disorders: From Genetic to Functional Pathways
Elisa Musto, Vivian W Y Liao, Katrine M Johannesen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 26, 2020
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids
Sacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, et al.
Developmental Cell
|
April 2, 2019
The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution
Deanne M Taylor, Bruce J Aronow, Kai Tan, et al.
Page
of 28
Search research articles
Search
Showing results (261-270 of 271) with videos related to
Sort By:
Page
of 28
European Journal of Human Genetics : EJHG
|
July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Mythily Ganapathi, Leticia S Matsuoka, Michael March, et al.
Journal of the American Heart Association
|
August 5, 2021
Rheumatic Heart Disease in the United States: Forgotten But Not Gone: Results of a 10 Year Multicenter Review
Sarah R de Loizaga, Lindsay Arthur, Bhawna Arya, et al.
Nature Communications
|
April 8, 2023
Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer
Mary C Bedard, Tafadzwa Chihanga, Adrean Carlile, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 16, 2016
Official American Thoracic Society/Japanese Respiratory Society Clinical Practice Guidelines: Lymphangioleiomyomatosis Diagnosis and Management
Francis X McCormack, Nishant Gupta, Geraldine R Finlay, et al.
Developmental Cell
|
December 22, 2021
A census of the lung: CellCards from LungMAP
Xin Sun, Anne-Karina Perl, Rongbo Li, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
June 11, 2026
International Society for Heart and Lung Transplantation Scientific Statement on pulmonary antibody-mediated rejection and proposed graft, antibody, and pathology (GAP) definition
Fiorella Calabrese, Deborah J Levine, Benjamin A Adam, et al.
Pediatric Blood & Cancer
|
July 22, 2025
High Prevalence of Abnormal Baseline Lung Function in Pediatric and Young Adult Hematopoietic Stem Cell Transplant Recipients: A Report from the TRANSPIRE Study
Jane Koo, Richard Cooper, Stephanie L Edwards, et al.
Annals of Neurology
|
August 22, 2023
GABRA1-Related Disorders: From Genetic to Functional Pathways
Elisa Musto, Vivian W Y Liao, Katrine M Johannesen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 26, 2020
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids
Sacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, et al.
Developmental Cell
|
April 2, 2019
The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution
Deanne M Taylor, Bruce J Aronow, Kai Tan, et al.
Page
of 28