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J M Puck

Showing results (71-80 of 99) with videos related to

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Bone Marrow Transplantation|April 25, 2017
Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCIDC 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 syndromeA 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, SCIDX1J 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 autoimmunityI 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 syndromeY 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 findingsM 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 lymphocytesT 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 apoptosisT 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 IIJ 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 infantsR H Buckley, R I Schiff, S E Schiff, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
Bone Marrow Transplantation|April 25, 2017
Unconditioned unrelated donor bone marrow transplantation for IL7Rα- and Artemis-deficient SCIDC 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 syndromeA 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, SCIDX1J 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 autoimmunityI 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 syndromeY 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 findingsM 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 lymphocytesT 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 apoptosisT 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 IIJ 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 infantsR H Buckley, R I Schiff, S E Schiff, et al.
Pageof 10