Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Edward Caparelli"'
1
Distinctive Clinicopathologic Features of Monomorphic B-cell Post-transplant Lymphoproliferative Disorders in Children
Autor: Michelle Gong, Rachel A. Mariani, Dawn A. Kirschmann, Edward Caparelli, Shunyou Gong, Nneka Wallace, Xinyan Lu, Rebekah Turner, Juehua Gao, Yanmin Zhang, Kai Lee Yap
Publikováno v: Pediatric and Developmental Pathology. 24:318-326
Introduction Post-transplant lymphoproliferative disorders (PTLDs) comprise a heterogeneous group of Epstein-Barr virus (EBV)-positive or negative lymphoid or plasmacytic lesions in solid organ or hematopoietic stem cell (HSC) transplant recipients.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a67c7a26aefa2569201b9798d63429d5
https://doi.org/10.1177/10935266211007254
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2
Detailed Phenotypic and Functional Characterization of a Rare, Antibody-Dependent SLAM-Associated Protein Expression Pattern
Autor: Michelle De Moura, Edward Caparelli, Wei Huang, Kai Lee Yap, Aaruni Khanolkar, Sabah Kadri, Asma Mustafa, Xiaotian T. Zheng, Jeffrey D. Wilks, Guorong Liu
Publikováno v: ImmunoHorizons. 4:153-164
SLAM-associated protein (SAP) is an adaptor molecule that facilitates critical effector functions in immune cells, and its deficiency causes X-linked lymphoproliferative disease type 1 in which effector responses directed against EBV are severely com
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc409e67c3f8da1a2fa581524c1605fa
https://doi.org/10.4049/immunohorizons.1900060
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3
A case of aberrant CD8 T cell-restricted IL-7 signaling with a Janus kinase 3 defect-associated atypical severe combined immunodeficiency
Autor: Guorong Liu, Ramsay L. Fuleihan, Jenna R.E. Bergerson, Bridget M. Simpson, Aaruni Khanolkar, Jeffrey D. Wilks, Edward Caparelli, Dawn A. Kirschmann
Publikováno v: Immunologic research. 68(1)
Severe combined immunodeficiency (SCID) disorders compromise lymphocyte numbers and/or function. One subset of SCID typically affects T cell and Natural Killer (NK) cell development in tandem (T-B+NK-) due to mutations arising in the genes encoding t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8d918e4128ff73615a69dffb7ab3baf
https://pubmed.ncbi.nlm.nih.gov/32215810
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4
Inv(11)(q21q23); KMT2A-MAML2, a Recurrent Genetic Abnormality in T-Cell Therapy-related Acute Lymphoblastic Leukemia
Autor: Joanna Weinstein, Rachel A. Mariani, Kai Lee Yap, Shunyou Gong, Edward Caparelli, Lawrence J. Jennings, Katrin M. Leuer, Mercedes Silva
Publikováno v: Journal of pediatric hematology/oncology. 42(4)
T-cell therapy-related acute lymphoblastic leukemia (T-t-ALL) is a rare condition associated with previous cytotoxic therapy for another disease. Here we report T-t-ALL with inv(11)(q21q23), which involves KMT2A and MAML2, a transcriptional coactivat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec00121a0c055876a8effe36e4136d73
https://pubmed.ncbi.nlm.nih.gov/31343482
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7
A novel HLA-A*30 allele, HLA-A*30:36
Autor: Edward Caparelli, J. E. Hall, Lawrence J. Jennings, Mercedes Silva, Min Yu
Publikováno v: Tissue antigens. 79(2)
A novel HLA allele, HLA-A*30:36, is found in a donor from the Central German Bone Marrow Donor Registry.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f73d9aa24b0bce3ab556dbeed6fd3c
https://pubmed.ncbi.nlm.nih.gov/22035629
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