Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia.
about
Recurrent pneumonia with mild hypogammaglobulinemia diagnosed as X-linked agammaglobulinemia in adultsCompeting modes of self-association in the regulatory domains of Bruton's tyrosine kinase: intramolecular contact versus asymmetric homodimerizationMolecular and structural characterization of five novel mutations in the Bruton's tyrosine kinase gene from patients with X-linked agammaglobulinemiaBTKbase, mutation database for X-linked agammaglobulinemia (XLA)BTKbase, mutation database for X-linked agammaglobulinemia (XLA).Src family protein tyrosine kinases induce autoactivation of Bruton's tyrosine kinase.A novel mutation (Cys145-->Stop) in Bruton's tyrosine kinase is associated with newly diagnosed X-linked agammaglobulinemia in a 51-year-old male.Discordant phenotype in siblings with X-linked agammaglobulinemia.Discovering cancer genes by integrating network and functional properties.Identification of novel Bruton's tyrosine kinase mutations in 10 unrelated subjects with X linked agammaglobulinaemiaEarly B cell defects.Immunodeficiency due to a unique protracted developmental delay in the B-cell lineageMutations in btk in patients with presumed X-linked agammaglobulinemia.Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains.Splice-correction strategies for treatment of X-linked agammaglobulinemia.Unusual patterns of exon skipping in Bruton tyrosine kinase are associated with mutations involving the intron 17 3' splice site.Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015).X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.BTK mutations selectively regulate BTK expression and upregulate monocyte XBP1 mRNA in XLA patientsOrganization and development of the immune system. Relation to its reconstruction.Interactions between protein kinase C and pleckstrin homology domains. Inhibition by phosphatidylinositol 4,5-bisphosphate and phorbol 12-myristate 13-acetate.A case of Fabry's disease with congenital agammaglobulinemia.Defective expression of Bruton's tyrosine kinase in acute lymphoblastic leukemia.Mutations of Bruton's tyrosine kinase gene in Brazilian patients with X-linked agammaglobulinemia.
P2860
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P2860
Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia.
description
1994 nî lūn-bûn
@nan
1994 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@ast
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@en
type
label
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@ast
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@en
prefLabel
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@ast
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@en
P2093
P2860
P356
P1476
Genomic organization and struc ...... ome-linked agammaglobulinemia.
@en
P2093
G W Litman
M de la Morena
R P Nelson
R T Litman
S J Kornfeld
P2860
P304
P356
10.1073/PNAS.91.19.9062
P407
P577
1994-09-01T00:00:00Z