Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Catherina Pan"'
Autor:
Katharina Shaw, Catherina Pan, Stephanie Sanchez‐Melendez, Dustin Taylor, Neda Shahriari, Lyn Duncan, Avery LaChance, Ruth Ann Vleugels
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 3, Pp 566-570 (2023)
Abstract Background Palmoplantar discoid lupus erythematosus (ppDLE) is a rare manifestation of chronic cutaneous lupus erythematosus that can result in painful, hyperkeratotic, and/or erosive lesions on the palms and soles. Despite this penchant to
Externí odkaz:
https://doaj.org/article/cc7b9922f78647dcbcfdd75865dde1ae
Publikováno v:
mBio, Vol 10, Iss 4 (2019)
ABSTRACT The formation of multimerized protein assemblies has emerged as a core component of immune signal amplification, yet the biochemical basis of this phenomenon remains unclear for many mammalian proteins within host defense pathways. The inter
Externí odkaz:
https://doaj.org/article/80cf4c532bf4458f95d35ee1f2e48a2c
Autor:
Qian Liu, Lizbeeth Lopez, Sandra Anaya-O'Brien, Jean Ulrick, Catherina Pan, Harry L. Malech, John S. Corns, Donald T. Ellenburg, Philip M. Murphy, Patricia Littel, Daniel Velez, David H. McDermott, Ji-Liang Gao
Publikováno v:
Journal of Clinical Immunology. 36:397-405
WHIM syndrome is an autosomal dominant immunodeficiency disease caused by mutations affecting the carboxy-terminus of CXCR4. To characterize novel genetic causes of the syndrome, we recruited a pediatric patient with possible WHIM syndrome, performed
Autor:
Daniel Velez, Donald T. Ellenburg, David H. McDermott, Harry L. Malech, Catherina Pan, Qian Liu, Philip M. Murphy, John S. Corns, Lizbeeth Lopez
Publikováno v:
Blood. 126:1003-1003
Introduction: WHIM syndrome is a rare autosomal dominant, primary immunodeficiency disease characterized by warts, hypogammaglobulinemia, infections and myelokathexis (impaired neutrophil egress from bone marrow resulting in neutropenia). Mutations i