Pages that link to "Q81310470"

The following pages link to Amy P Hsu (Q81310470):

Displaying 32 items.

• STAT3 mutations in the hyper-IgE syndrome (Q28249785) (← links)
• GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome (Q28704337) (← links)
• Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome. (Q34192317) (← links)
• Interleukin-12 receptor β1 deficiency predisposing to disseminated Coccidioidomycosis (Q34699215) (← links)
• GATA2 deficiency-associated bone marrow disorder differs from idiopathic aplastic anemia. (Q34802461) (← links)
• GATA2 deficiency. (Q35127953) (← links)
• Clonal Diversification and Changes in Lipid Traits and Colony Morphology in Mycobacterium abscessus Clinical Isolates (Q35751576) (← links)
• IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotype. (Q35858596) (← links)
• Cis-element mutated in GATA2-dependent immunodeficiency governs hematopoiesis and vascular integrity (Q36290255) (← links)
• Reversion mutations in patients with leukocyte adhesion deficiency type-1 (LAD-1) (Q36384593) (← links)
• GATA2 deficiency underlying severe blastomycosis and fatal herpes simplex virus-associated hemophagocytic lymphohistiocytosis (Q36563645) (← links)
• Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset. (Q36743341) (← links)
• Association of GATA2 Deficiency With Severe Primary Epstein-Barr Virus (EBV) Infection and EBV-associated Cancers (Q36991772) (← links)
• Extrapulmonary Aspergillus infection in patients with CARD9 deficiency. (Q37351602) (← links)
• GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity. (Q37564756) (← links)
• Persistent nodal histoplasmosis in nuclear factor kappa B essential modulator deficiency: Report of a case and review of infection in primary immunodeficiencies. (Q38856369) (← links)
• Cytoskeletal abnormalities and neutrophil dysfunction in WDR1 deficiency (Q40480653) (← links)
• Distinct mutations at the same positions of STAT3 cause either loss or gain of function (Q40636507) (← links)
• Adenosine deaminase type 2 deficiency masquerading as GATA2 deficiency: Successful hematopoietic stem cell transplantation. (Q40693114) (← links)
• IKBKG (NEMO) 5' untranslated splice mutations lead to severe, chronic disseminated mycobacterial infections. (Q52657952) (← links)
• (p47)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis (Q60907706) (← links)
• Aspergillosis, eosinophilic esophagitis, and allergic rhinitis in signal transducer and activator of transcription 3 haploinsufficiency (Q88872572) (← links)
• Somatic mutations in children with GATA2-associated myelodysplastic syndrome who lack other features of GATA2 deficiency (Q89777936) (← links)
• A review of innate and adaptive immunity to coccidioidomycosis (Q91252710) (← links)
• Dominant activating RAC2 mutation with lymphopenia, immunodeficiency, and cytoskeletal defects (Q91360570) (← links)
• Donor-derived MDS/AML in families with germline GATA2 mutation (Q91553288) (← links)
• Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections (Q91886016) (← links)
• STAT1 Gain-of-Function Mutations Cause High Total STAT1 Levels With Normal Dephosphorylation (Q92239199) (← links)
• Lymphocyte-driven regional immunopathology in pneumonitis caused by impaired central immune tolerance (Q92547335) (← links)
• Prospective Study of a Novel, Radiation-Free, Reduced-Intensity Bone Marrow Transplantation Platform for Primary Immunodeficiency Diseases (Q93166388) (← links)
• MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation (Q93382514) (← links)
• Autosomal Dominant Hyper IgE Syndrome (Q94995200) (← links)