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Bone Marrow Transplantation
|
April 25, 2017
Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCID
C C Dvorak, K Patel, J M Puck, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
|
February 16, 2000
Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome
A C O'Connell, J M Puck, B Grimbacher, et al.
Human Molecular Genetics
|
August 1, 1993
The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1
J M Puck, S M Deschênes, J C Porter, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
February 15, 1997
Characteristic T helper 2 T cell cytokine abnormalities in autoimmune lymphoproliferative syndrome, a syndrome marked by defective apoptosis and humoral autoimmunity
I J Fuss, W Strober, J K Dale, et al.
Clinical Immunology (Orlando, Fla.)
|
September 25, 1999
Expression in transgenic mice of dominant interfering Fas mutations: a model for human autoimmune lymphoproliferative syndrome
Y Choi, V R Ramnath, A S Eaton, et al.
The Journal of Clinical Investigation
|
May 1, 1990
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings
M E Conley, R H Buckley, R Hong, et al.
Blood
|
August 26, 1998
Retroviral marking of canine bone marrow: long-term, high-level expression of human interleukin-2 receptor common gamma chain in canine lymphocytes
T Whitwam, M E Haskins, P S Henthorn, et al.
Clinical Reviews in Allergy & Immunology
|
March 28, 2001
The autoimmune lymphoproliferative syndrome. A disorder of human lymphocyte apoptosis
T A Fleisher, J M Puck, W Strober, et al.
Cell
|
July 21, 1999
Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II
J Wang, L Zheng, A Lobito, et al.
The Journal of Pediatrics
|
March 1, 1997
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants
R H Buckley, R I Schiff, S E Schiff, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 99) with videos related to
Sort By:
Page
of 10
Bone Marrow Transplantation
|
April 25, 2017
Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCID
C C Dvorak, K Patel, J M Puck, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics
|
February 16, 2000
Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome
A C O'Connell, J M Puck, B Grimbacher, et al.
Human Molecular Genetics
|
August 1, 1993
The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1
J M Puck, S M Deschênes, J C Porter, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
February 15, 1997
Characteristic T helper 2 T cell cytokine abnormalities in autoimmune lymphoproliferative syndrome, a syndrome marked by defective apoptosis and humoral autoimmunity
I J Fuss, W Strober, J K Dale, et al.
Clinical Immunology (Orlando, Fla.)
|
September 25, 1999
Expression in transgenic mice of dominant interfering Fas mutations: a model for human autoimmune lymphoproliferative syndrome
Y Choi, V R Ramnath, A S Eaton, et al.
The Journal of Clinical Investigation
|
May 1, 1990
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings
M E Conley, R H Buckley, R Hong, et al.
Blood
|
August 26, 1998
Retroviral marking of canine bone marrow: long-term, high-level expression of human interleukin-2 receptor common gamma chain in canine lymphocytes
T Whitwam, M E Haskins, P S Henthorn, et al.
Clinical Reviews in Allergy & Immunology
|
March 28, 2001
The autoimmune lymphoproliferative syndrome. A disorder of human lymphocyte apoptosis
T A Fleisher, J M Puck, W Strober, et al.
Cell
|
July 21, 1999
Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II
J Wang, L Zheng, A Lobito, et al.
The Journal of Pediatrics
|
March 1, 1997
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants
R H Buckley, R I Schiff, S E Schiff, et al.
Page
of 10