نتایج جستجو برای: lyp

تعداد نتایج: 229  

Journal: :The Journal of clinical investigation 2013
Xuezhi Dai Richard G James Tania Habib Swati Singh Shaun Jackson Socheath Khim Randall T Moon Denny Liggitt Alejandro Wolf-Yadlin Jane H Buckner David J Rawlings

Multiple autoimmune diseases, including type 1 diabetes, rheumatoid arthritis, Graves disease, and systemic lupus erythematosus, are associated with an allelic variant of protein tyrosine phosphatase nonreceptor 22 (PTPN22), which encodes the protein LYP. To model the human disease-linked variant LYP-R620W, we generated knockin mice expressing the analogous mutation, R619W, in the murine orthol...

Journal: :Diabetes 2002
Sheela Ramanathan Marie-Therese Bihoreau Andrew D Paterson Leili Marandi Dominique Gauguier Philippe Poussier

Spontaneous type 1 diabetes in BB rats is dependent on the RT1(u) MHC haplotype and homozygosity for an allele at the Lyp locus, which is responsible for a peripheral T-lymphopenia. Genetic studies have shown that there are other, as yet unidentified, genetic loci contributing to diabetes susceptibility in this strain. BB rats carrying wild-type Lyp alleles are not lymphopenic and are resistant...

Journal: :Journal of immunology 2009
Julie Zikherman Michelle Hermiston David Steiner Kiminori Hasegawa Andrew Chan Arthur Weiss

Pep and CD45 are tyrosine phosphatases whose targets include the Src-family kinases, critical mediators of Ag receptor signaling. A polymorphism in PTPN22, the gene that encodes the human Pep orthologue Lyp, confers susceptibility to multiple human autoimmune diseases in the context of complex genetic backgrounds. However, the functional significance of the R620W risk allele is not clear. We re...

2005
Weipeng Zheng Jin-Xiong She

The lymphoid-specific phosphatase (LYP) encoded by PTPN22 is involved in preventing spontaneous T-cell activation by dephosphorylating and inactivating T-cell receptor–associated Csk kinase. We have genotyped 396 type 1 diabetic patients and 1,178 control subjects of Caucasian descent from north central Florida and report a strong association between type 1 diabetes and a polymorphism (R620W) i...

Journal: :Blood 1998
M Beylot-Barry A Groppi B Vergier K Pulford J P Merlio

NPM-ALK chimeric transcripts, encoded by the t(2;5), lead to an aberrant expression of ALK by CD30+ systemic lymphomas. To determine if t(2;5) is involved in cutaneous lymphoproliferative disorders, we studied 37 CD30+ cutaneous lymphoproliferations, 27 mycosis fungoides (MF), and 16 benign inflammatory disorders (BID). NPM-ALK transcripts were detected by nested reverse transcription-polymeras...

2017
Kerasia-Maria Plachouri Carsten Weishaupt Dieter Metze Georg Evers Wolfgang E. Berdel Werner Kempf Cord Sunderkötter Matthias Stelljes

CHOEP: chemotherapy with cyclophosphamide doxorubicin, etoposide, vincristine, and prednisone CTCL: cutaneous T-cell lymphoma HLA: human leukocyte antigen HSCT: hematopoietic stem cell transplantation LyP: lymphomatoid papulosis INTRODUCTION We report a case of a fulminant cutaneous cytotoxic T-cell lymphoma nonresponsive to chemotherapy but showing durable complete response to a fast sequence ...

Journal: :Journal of immunology 1999
S Ramanathan P Poussier

One of the diabetes susceptibility genes of the BB/W (Biobreeding/Worcester) rat maps to the lyp locus on chromosome 4. The BB/W lyp allele is responsible for a severe peripheral T lymphopenia. Correction of this lymphopenia by transfer of normal, histocompatible T cells prevents diabetes, providing T cell reconstitution is initiated before insulitis. We have analyzed this time-dependent regula...

Journal: :Clinical and Developmental Immunology 2005
Sabine Oertelt Thomas P. Kenny Carlo Selmi Pietro Invernizzi Mauro Podda M. Eric Gershwin

Previous studies on primary biliary cirrhosis (PBC) have focused on the role of T lymphocytes as potential effectors of tissue injury. We hypothesized that single nucleotide polymorphisms (SNPs) of genes involved in lymphocyte proliferation would be responsible for uncontrolled expansion of T cells and autoreactivity. To address this, we genotyped DNA from 154 patients with PBC and 166 ethnical...

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