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Research and Practice in Thrombosis and Haemostasis
|
June 9, 2025
Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders
Veysel Gök, Alper Ozcan, Fatma Türkan Mutlu, et al.
Clinical and Translational Allergy
|
January 5, 2018
European Summit on the Prevention and Self-Management of Chronic Respiratory Diseases: report of the European Union Parliament Summit (29 March 2017)
Peter W Hellings, David Borrelli, Sirpa Pietikainen, et al.
The Journal of Allergy and Clinical Immunology
|
July 30, 2025
CARMIL2 deficiency disrupts activation-induced metabolic reprogramming in T cells and is partially rescued by glutamine supplementation
Mona Kabha, Maya Liaks-Bohnick, Fadia Zagairy, et al.
The Lancet. Infectious Diseases
|
July 28, 2015
The Israeli public health response to wild poliovirus importation
Ehud Kaliner, Eran Kopel, Emilia Anis, et al.
The Journal of Pediatrics
|
October 27, 2018
As Few Pediatricians as Possible and as Many Pediatricians as Necessary?
Jochen Ehrich, Laila Burla, Angel Carrasco Sanz, et al.
Nature Communications
|
February 27, 2020
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
Nature Communications
|
April 22, 2020
Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
Biorxiv : the Preprint Server for Biology
|
September 25, 2023
Robust and scalable single-molecule protein sequencing with fluorosequencing
James H Mapes, Julia Stover, Heather D Stout, et al.
The Journal of Experimental Medicine
|
November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects
Atar Lev, Yu Nee Lee, Guangping Sun, et al.
Cell Death & Disease
|
January 12, 2026
Mutations in VPS18 lead to a neutrophil maturation defect associated with disturbed vesicle homeostasis
Jincheng Gao, Almke Bader, Monika I Linder, et al.
Page
of 36
Search research articles
Search
Showing results (331-340 of 353) with videos related to
Sort By:
Page
of 36
Research and Practice in Thrombosis and Haemostasis
|
June 9, 2025
Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders
Veysel Gök, Alper Ozcan, Fatma Türkan Mutlu, et al.
Clinical and Translational Allergy
|
January 5, 2018
European Summit on the Prevention and Self-Management of Chronic Respiratory Diseases: report of the European Union Parliament Summit (29 March 2017)
Peter W Hellings, David Borrelli, Sirpa Pietikainen, et al.
The Journal of Allergy and Clinical Immunology
|
July 30, 2025
CARMIL2 deficiency disrupts activation-induced metabolic reprogramming in T cells and is partially rescued by glutamine supplementation
Mona Kabha, Maya Liaks-Bohnick, Fadia Zagairy, et al.
The Lancet. Infectious Diseases
|
July 28, 2015
The Israeli public health response to wild poliovirus importation
Ehud Kaliner, Eran Kopel, Emilia Anis, et al.
The Journal of Pediatrics
|
October 27, 2018
As Few Pediatricians as Possible and as Many Pediatricians as Necessary?
Jochen Ehrich, Laila Burla, Angel Carrasco Sanz, et al.
Nature Communications
|
February 27, 2020
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
Nature Communications
|
April 22, 2020
Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, et al.
Biorxiv : the Preprint Server for Biology
|
September 25, 2023
Robust and scalable single-molecule protein sequencing with fluorosequencing
James H Mapes, Julia Stover, Heather D Stout, et al.
The Journal of Experimental Medicine
|
November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects
Atar Lev, Yu Nee Lee, Guangping Sun, et al.
Cell Death & Disease
|
January 12, 2026
Mutations in VPS18 lead to a neutrophil maturation defect associated with disturbed vesicle homeostasis
Jincheng Gao, Almke Bader, Monika I Linder, et al.
Page
of 36