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The Journal of Experimental Medicine
|
November 9, 2018
PRC2 loss induces chemoresistance by repressing apoptosis in T cell acute lymphoblastic leukemia
Ingrid M Ariës, Kimberly Bodaar, Salmaan A Karim, et al.
European Journal of Medical Genetics
|
March 3, 2009
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, et al.
The Review of Scientific Instruments
|
October 7, 2011
Invited article: millimeter-wave bolometer array receiver for the Atacama pathfinder experiment Sunyaev-Zel'dovich (APEX-SZ) instrument
D Schwan, P A R Ade, K Basu, et al.
Science (New York, N.Y.)
|
September 18, 2020
(Sub)stellar companions shape the winds of evolved stars
L Decin, M Montargès, A M S Richards, et al.
Nature Genetics
|
September 19, 2018
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation
M Felicia Basilicata, Ange-Line Bruel, Giuseppe Semplicio, et al.
MMWR. Morbidity and Mortality Weekly Report
|
November 27, 2014
Antiretroviral therapy enrollment characteristics and outcomes among HIV-infected adolescents and young adults compared with older adults--seven African countries, 2004-2013
Andrew F Auld, Simon G Agolory, Ray W Shiraishi, et al.
Plos Neglected Tropical Diseases
|
May 4, 2022
Combining rapid diagnostic tests to estimate primary and post-primary dengue immune status at the point of care
Joseph R Biggs, Ava Kristy Sy, James Ashall, et al.
Cell Reports. Medicine
|
April 16, 2024
Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum
Joline Ingels, Laurenz De Cock, Dieter Stevens, et al.
Journal of Medical Genetics
|
July 24, 2017
<i>FOXP1</i>-related intellectual disability syndrome: a recognisable entity
Ilse Meerschaut, Daniel Rochefort, Nicole Revençu, et al.
American Journal of Human Genetics
|
April 15, 2014
Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems
Anneke T Vulto-van Silfhout, Shivakumar Rajamanickam, Philip J Jensik, et al.
Page
of 58
Search research articles
Search
Showing results (551-560 of 571) with videos related to
Sort By:
Page
of 58
The Journal of Experimental Medicine
|
November 9, 2018
PRC2 loss induces chemoresistance by repressing apoptosis in T cell acute lymphoblastic leukemia
Ingrid M Ariës, Kimberly Bodaar, Salmaan A Karim, et al.
European Journal of Medical Genetics
|
March 3, 2009
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, et al.
The Review of Scientific Instruments
|
October 7, 2011
Invited article: millimeter-wave bolometer array receiver for the Atacama pathfinder experiment Sunyaev-Zel'dovich (APEX-SZ) instrument
D Schwan, P A R Ade, K Basu, et al.
Science (New York, N.Y.)
|
September 18, 2020
(Sub)stellar companions shape the winds of evolved stars
L Decin, M Montargès, A M S Richards, et al.
Nature Genetics
|
September 19, 2018
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation
M Felicia Basilicata, Ange-Line Bruel, Giuseppe Semplicio, et al.
MMWR. Morbidity and Mortality Weekly Report
|
November 27, 2014
Antiretroviral therapy enrollment characteristics and outcomes among HIV-infected adolescents and young adults compared with older adults--seven African countries, 2004-2013
Andrew F Auld, Simon G Agolory, Ray W Shiraishi, et al.
Plos Neglected Tropical Diseases
|
May 4, 2022
Combining rapid diagnostic tests to estimate primary and post-primary dengue immune status at the point of care
Joseph R Biggs, Ava Kristy Sy, James Ashall, et al.
Cell Reports. Medicine
|
April 16, 2024
Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum
Joline Ingels, Laurenz De Cock, Dieter Stevens, et al.
Journal of Medical Genetics
|
July 24, 2017
<i>FOXP1</i>-related intellectual disability syndrome: a recognisable entity
Ilse Meerschaut, Daniel Rochefort, Nicole Revençu, et al.
American Journal of Human Genetics
|
April 15, 2014
Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems
Anneke T Vulto-van Silfhout, Shivakumar Rajamanickam, Philip J Jensik, et al.
Page
of 58