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Frontiers in Pediatrics
|
March 22, 2024
Case Report: Profound newborn leukopenia related to a novel RAC2 variant
Geoffrey Hall, Ágnes Donkó, Cristina Pratt, et al.
Journal of Clinical Immunology
|
April 16, 2011
Coronary artery abnormalities in Hyper-IgE syndrome
Alexandra F Freeman, Elizabeth Mannino Avila, Pamela A Shaw, et al.
The American Journal of Cardiology
|
March 4, 2008
Meta-analysis comparing reported frequency of atrial fibrillation after acute coronary syndromes in Asians versus whites
Gian M Novaro, Craig R Asher, Deepak L Bhatt, et al.
Blood
|
August 6, 2011
Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency
Jennifer Cuellar-Rodriguez, Juan Gea-Banacloche, Alexandra F Freeman, et al.
Blood
|
March 19, 2013
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
Amy P Hsu, Kirby D Johnson, E Liana Falcone, et al.
Immunity
|
November 29, 2011
A critical role for STAT3 transcription factor signaling in the development and maintenance of human T cell memory
Andrea M Siegel, Jennifer Heimall, Alexandra F Freeman, et al.
Blood Advances
|
September 16, 2021
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome
Robert R West, Katherine R Calvo, Lisa J Embree, et al.
Journal of Clinical Immunology
|
March 23, 2012
A novel STAT1 mutation associated with disseminated mycobacterial disease
Elizabeth P Sampaio, Hannelore I Bax, Amy P Hsu, et al.
British Journal of Haematology
|
November 12, 2019
GATA2 deficiency and haematopoietic stem cell transplantation: challenges for the clinical practitioner
Delfien J Bogaert, Genevieve Laureys, Leslie Naesens, et al.
Stem Cell Research
|
November 11, 2019
Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation
Hui Jin, Zhen Yu, Keron Navarengom, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 150) with videos related to
Sort By:
Page
of 15
Frontiers in Pediatrics
|
March 22, 2024
Case Report: Profound newborn leukopenia related to a novel RAC2 variant
Geoffrey Hall, Ágnes Donkó, Cristina Pratt, et al.
Journal of Clinical Immunology
|
April 16, 2011
Coronary artery abnormalities in Hyper-IgE syndrome
Alexandra F Freeman, Elizabeth Mannino Avila, Pamela A Shaw, et al.
The American Journal of Cardiology
|
March 4, 2008
Meta-analysis comparing reported frequency of atrial fibrillation after acute coronary syndromes in Asians versus whites
Gian M Novaro, Craig R Asher, Deepak L Bhatt, et al.
Blood
|
August 6, 2011
Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency
Jennifer Cuellar-Rodriguez, Juan Gea-Banacloche, Alexandra F Freeman, et al.
Blood
|
March 19, 2013
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
Amy P Hsu, Kirby D Johnson, E Liana Falcone, et al.
Immunity
|
November 29, 2011
A critical role for STAT3 transcription factor signaling in the development and maintenance of human T cell memory
Andrea M Siegel, Jennifer Heimall, Alexandra F Freeman, et al.
Blood Advances
|
September 16, 2021
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome
Robert R West, Katherine R Calvo, Lisa J Embree, et al.
Journal of Clinical Immunology
|
March 23, 2012
A novel STAT1 mutation associated with disseminated mycobacterial disease
Elizabeth P Sampaio, Hannelore I Bax, Amy P Hsu, et al.
British Journal of Haematology
|
November 12, 2019
GATA2 deficiency and haematopoietic stem cell transplantation: challenges for the clinical practitioner
Delfien J Bogaert, Genevieve Laureys, Leslie Naesens, et al.
Stem Cell Research
|
November 11, 2019
Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation
Hui Jin, Zhen Yu, Keron Navarengom, et al.
Page
of 15