About: Jennifer M Puck

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	Forscher (de) researcher (en) investigador (es) chercheur (fr) wetenschapper (nl) дослідниця (uk) 研究者 (zh) 研究員 (ja)
rdfs:label	Jennifer M Puck (en) Jennifer M Puck (nl) Jennifer Puck (cs)
skos:prefLabel	Jennifer M Puck (en) Jennifer M Puck (nl) Jennifer Puck (cs)
name	Jennifer M Puck (en) Jennifer M Puck (nl) Jennifer Puck (cs)
given name	wds:Q96203363-6718EF98-807A-40B9-9877-474FC9A78323
given name	Jennifer
instance of	wds:Q96203363-86F75671-8AFF-4EB3-8049-8237F50B16C6
NL CR AUT ID	wds:Q96203363-131684ED-76F5-4E25-9235-BA3E9E493880
instance of	Homo sapiens
NL CR AUT ID	uk2007369606
skos:altLabel	Jennifer Puck (en)
occupation	wds:Q96203363-4576D708-53A7-4EBD-A027-0CA3453BACB8
sex or gender	wds:Q96203363-9DB84B3F-CBBA-43D3-A0A4-D8E89570E8AB
ISNI	wds:Q96203363-E7D03983-F8EA-47A2-A6B5-39F922BDC655
VIAF ID	wds:Q96203363-85F4749F-AC1F-4A7D-976F-F097D034376B
Library of Congress authority ID	wds:Q96203363-5163B6B9-36AD-461F-AEC0-2EBDDF1ADF1B
IdRef ID	wds:Q96203363-804B531D-5E45-432F-A753-6A39E668364A
date of birth	wds:Q96203363-3C1B51E2-E87E-4DD7-8271-85FF47FF7012
National Library of Israel J9U ID	wds:Q96203363-E3AA99A0-3ED8-4F1A-AE71-7C2CD48A53C7
VIAF ID	http://viaf.org/viaf/69099794
Library of Congress authority ID	http://id.loc.gov/authorities/names/n97803609
IdRef ID	http://www.idref.fr/050509071/id
occupation	researcher
sex or gender	female organism
ISNI	0000000114930936
VIAF ID	69099794
Library of Congress authority ID	n97803609
IdRef ID	050509071
date of birth	1949-01-01 00:00:00Z (xsd:dateTime)
National Library of Israel J9U ID	987007314844605171
ORCID iD	wds:Q96203363-1CA9125C-8FA1-496F-9228-02531BA10752
ORCID iD	https://orcid.org/0000-0001-6623-6276
ORCID iD	0000-0001-6623-6276
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q96203363
is author of	STAT3 mutations in the hyper-IgE syndrome Bone density and fractures in autosomal dominant hyper IgE syndrome Dermatitis and the newborn rash of hyper-IgE syndrome Brain abnormalities in patients with hyperimmunoglobulin E syndrome. Causes of death in hyper-IgE syndrome. Coronin-1A: immune deficiency in humans and mice Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Perspectives of gene therapy for primary immunodeficiencies Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations Primary immunodeficiencies: 2009 update Newborn screening for SCID identifies patients with ataxia telangiectasia Development of population-based newborn screening for severe combined immunodeficiency Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency Population-based newborn screening for severe combined immunodeficiency: steps toward implementation Laboratory technology for population-based screening for severe combined immunodeficiency in neonates: the winner is T-cell receptor excision circles Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation The hyper-IgE syndrome is not caused by a microdeletion syndrome. Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a Coronin-1A mutation and a chromosome 16p11.2 deletion Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005 The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity The case for newborn screening for severe combined immunodeficiency and related disorders Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency Use of rituximab for refractory cytopenias associated with autoimmune lymphoproliferative syndrome (ALPS) Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency Pyrimethamine treatment does not ameliorate lymphoproliferation or autoimmune disease in MRL/lpr-/- mice or in patients with autoimmune lymphoproliferative syndrome Use of mycophenolate mofetil for chronic, refractory immune cytopenias in children with autoimmune lymphoproliferative syndrome NRAS mutation causes a human autoimmune lymphoproliferative syndrome. Fluorodeoxyglucose positron emission tomography (FDG-PET) for monitoring lymphadenopathy in the autoimmune lymphoproliferative syndrome (ALPS). Biotechnology. A prudent path forward for genomic engineering and germline gene modification Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome Successes and risks of gene therapy in primary immunodeficiencies Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015. Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome Histologic features of sinus histiocytosis with massive lymphadenopathy in patients with autoimmune lymphoproliferative syndrome A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID). Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome Improving cellular therapy for primary immune deficiency diseases: recognition, diagnosis, and management Cellular calibrators to quantitate T-cell receptor excision circles (TRECs) in clinical samples B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients. X Inactivation in Females with X-Linked Disease Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency Induction of apoptosis and activation of NF-kappaB by CD95 require different signalling thresholds IL-21 is the primary common γ chain-binding cytokine required for human B-cell differentiation in vivo Recombinant human hyaluronidase-facilitated subcutaneous infusion of human immunoglobulins for primary immunodeficiency

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