Search research articles
Contact Us
Filters
Showing results (81-90 of 152) with videos related to
Page
of 16
Sort By:
Human Molecular Genetics
|
December 1, 1995
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
T Attié, M Till, A Pelet, et al.
Annals of Thoracic Surgery Short Reports
|
January 10, 2025
Global Cardiac Surgical Volume and Gaps: Trends, Targets, and Way Forward
Dominique Vervoort, Grace Lee, Hiba Ghandour, et al.
Innovations (Philadelphia, Pa.)
|
December 13, 2023
Upper Hemisternotomy Versus Full Sternotomy for Replacement of the Supracoronary Ascending Aorta and Aortic Valve
Vishal N Shah, Jose Binongo, Jane Wei, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 7, 2005
[Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases]
E André, M Till, P Descargues, et al.
Elife
|
January 16, 2020
A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency
Tara L Mastro, Anthony Preza, Shinjini Basu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1993
Analysis of human immunodeficiency virus-infected tissues by amplification and in situ hybridization reveals latent and permissive infections at single-cell resolution
J Embretson, M Zupancic, J Beneke, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
September 10, 2022
Impact of stereotactic body radiation therapy volume on surgical patient selection, short-term survival, and long-term survival in early-stage non-small cell lung cancer
Brian M Till, Shale Mack, Gregory Whitehorn, et al.
Clinical Genetics
|
November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
L Michel-Calemard, F Dijoud, M Till, et al.
Prenatal Diagnosis
|
January 22, 2005
Prenatal diagnosis of Aicardi-Goutières syndrome
M Le Garrec, M Doret, J C Pasquier, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 18, 2026
Strain-level antigen variation facilitates immune evasion in Bacteroides thetaiotaomicron
Robert W P Glowacki, Jessica M Till, Orion D Brock, et al.
Page
of 16
Search research articles
Search
Showing results (81-90 of 152) with videos related to
Sort By:
Page
of 16
Human Molecular Genetics
|
December 1, 1995
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
T Attié, M Till, A Pelet, et al.
Annals of Thoracic Surgery Short Reports
|
January 10, 2025
Global Cardiac Surgical Volume and Gaps: Trends, Targets, and Way Forward
Dominique Vervoort, Grace Lee, Hiba Ghandour, et al.
Innovations (Philadelphia, Pa.)
|
December 13, 2023
Upper Hemisternotomy Versus Full Sternotomy for Replacement of the Supracoronary Ascending Aorta and Aortic Valve
Vishal N Shah, Jose Binongo, Jane Wei, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 7, 2005
[Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases]
E André, M Till, P Descargues, et al.
Elife
|
January 16, 2020
A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency
Tara L Mastro, Anthony Preza, Shinjini Basu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1993
Analysis of human immunodeficiency virus-infected tissues by amplification and in situ hybridization reveals latent and permissive infections at single-cell resolution
J Embretson, M Zupancic, J Beneke, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
September 10, 2022
Impact of stereotactic body radiation therapy volume on surgical patient selection, short-term survival, and long-term survival in early-stage non-small cell lung cancer
Brian M Till, Shale Mack, Gregory Whitehorn, et al.
Clinical Genetics
|
November 22, 2008
Pseudoexon activation in the PKHD1 gene: a French founder intronic mutation IVS46+653A>G causing severe autosomal recessive polycystic kidney disease
L Michel-Calemard, F Dijoud, M Till, et al.
Prenatal Diagnosis
|
January 22, 2005
Prenatal diagnosis of Aicardi-Goutières syndrome
M Le Garrec, M Doret, J C Pasquier, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 18, 2026
Strain-level antigen variation facilitates immune evasion in Bacteroides thetaiotaomicron
Robert W P Glowacki, Jessica M Till, Orion D Brock, et al.
Page
of 16