Her main research concerns Immunology, Primary immunodeficiency, Severe combined immunodeficiency, Genetics and Autoimmune lymphoproliferative syndrome. Her Immunology study is mostly concerned with Job Syndrome, Immune system, Immunopathology, Lymphocyte and Immunodeficiency. Jennifer M. Puck interconnects Lymphocyte proliferation, Immunologic Deficiency Syndromes and Family medicine in the investigation of issues within Primary immunodeficiency.
Her Severe combined immunodeficiency research is multidisciplinary, relying on both Hematopoietic stem cell transplantation, Transplantation, Bone marrow and T-cell receptor excision circles. In Genetics, Jennifer M. Puck works on issues like Molecular biology, which are connected to Gene, Somatic cell, Mutant and CD3 Complex. The various areas that Jennifer M. Puck examines in her Autoimmune lymphoproliferative syndrome study include Fas ligand, Lymphoma and Lymphocyte homeostasis.
Jennifer M. Puck mainly investigates Immunology, Severe combined immunodeficiency, Primary immunodeficiency, Genetics and Newborn screening. Her research integrates issues of Mutation and Autoimmune lymphoproliferative syndrome in her study of Immunology. Her work investigates the relationship between Autoimmune lymphoproliferative syndrome and topics such as Autoimmune disease that intersect with problems in Autoimmunity.
Her Severe combined immunodeficiency study incorporates themes from Hematopoietic stem cell transplantation, Transplantation, Genetic enhancement and T-cell receptor excision circles. Her Primary immunodeficiency research incorporates elements of Recombinant Human Hyaluronidase, Immunologic Deficiency Syndromes and Intensive care medicine. Within one scientific family, Jennifer M. Puck focuses on topics pertaining to Molecular biology under Genetics, and may sometimes address concerns connected to Mutant and Lymphocyte.
Jennifer M. Puck mainly investigates Severe combined immunodeficiency, Immunology, Newborn screening, Immune system and Transplantation. The concepts of her Severe combined immunodeficiency study are interwoven with issues in Hematopoietic stem cell transplantation, Busulfan, DCLRE1C, B cell and Genetic enhancement. She applies her multidisciplinary studies on Immunology and In patient in her research.
She works mostly in the field of Newborn screening, limiting it down to topics relating to Exome sequencing and, in certain cases, DNA sequencing. Her research in Transplantation intersects with topics in Hematopoietic cell, Omenn syndrome and Rituximab. Her Primary immunodeficiency study integrates concerns from other disciplines, such as Antibody and Intensive care medicine.
Her main research concerns Severe combined immunodeficiency, Transplantation, Newborn screening, Hematopoietic stem cell transplantation and Immunology. Her work deals with themes such as Immune system, Genetic enhancement and Pediatrics, which intersect with Severe combined immunodeficiency. Her study looks at the relationship between Newborn screening and fields such as T-cell receptor excision circles, as well as how they intersect with chemical problems.
Her Hematopoietic stem cell transplantation study combines topics from a wide range of disciplines, such as DCLRE1C and Oncology. Her Immunology research incorporates themes from Transplantation Conditioning and Busulfan. Her Primary immunodeficiency study combines topics in areas such as Immunologic Deficiency Syndromes and Family medicine.
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Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome
Galen H Fisher;Fredric J Rosenberg;Stephen E Straus;Janet K Dale.
Cell (1995)
STAT3 Mutations in the Hyper-IgE Syndrome
Steven M. Holland;Frank R. DeLeo;Houda Z. Elloumi;Amy P. Hsu.
The New England Journal of Medicine (2007)
Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem Disorder
Bodo Grimbacher;Steven M. Holland;John I. Gallin;Frank Greenberg.
The New England Journal of Medicine (1999)
A prudent path forward for genomic engineering and germline gene modification
David Baltimore;Paul Berg;Michael Botchan;Dana Carroll.
Science (2015)
Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency
Hyung J. Chun;Lixin Zheng;Manzoor Ahmad;Jin Wang;Jin Wang.
Nature (2002)
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.
Rebecca H. Buckley;Richard I. Schiff;Sherrie E. Schiff;M.Louise Markert.
The Journal of Pediatrics (1997)
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015
Capucine Picard;Waleed Al-Herz;Aziz Bousfiha;Jean Laurent Casanova.
Journal of Clinical Immunology (2015)
Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II
Jin Wang;Lixin Zheng;Adrian Lobito;Francis Ka Ming Chan.
Cell (1999)
Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel.
Frontiers in Immunology (2014)
Primary immunodeficiencies: 2009 update
Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova.
The Journal of Allergy and Clinical Immunology (2009)
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