148 related articles for article (PubMed ID: 11686883)
21. Uncovering Low-Level Maternal Gonosomal Mosaicism in X-Linked Agammaglobulinemia: Implications for Genetic Counseling.
Rivière JG; Franco-Jarava C; Martínez-Gallo M; Aguiló-Cucurull A; Blasco-Pérez L; Paramonov I; Antolín M; Martín-Nalda A; Soler-Palacín P; Colobran R
Front Immunol; 2020; 11():46. PubMed ID: 32117230
[TBL] [Abstract][Full Text] [Related]
22. A novel Bruton's tyrosine kinase gene (BTK) invariant splice site mutation in a Malaysian family with X-linked agammaglobulinemia.
Chear CT; Gill HK; Ramly NH; Dhaliwal JS; Bujang N; Ripen AM; Mohamad SB
Asian Pac J Allergy Immunol; 2013 Dec; 31(4):320-4. PubMed ID: 24383975
[TBL] [Abstract][Full Text] [Related]
23. Discordant phenotype in siblings with X-linked agammaglobulinemia.
Bykowsky MJ; Haire RN; Ohta Y; Tang H; Sung SS; Veksler ES; Greene JM; Fu SM; Litman GW; Sullivan KE
Am J Hum Genet; 1996 Mar; 58(3):477-83. PubMed ID: 8644706
[TBL] [Abstract][Full Text] [Related]
24. Molecular and structural characterization of five novel mutations in the Bruton's tyrosine kinase gene from patients with X-linked agammaglobulinemia.
Saha BK; Curtis SK; Vogler LB; Vihinen M
Mol Med; 1997 Jul; 3(7):477-85. PubMed ID: 9260159
[TBL] [Abstract][Full Text] [Related]
25. Identification of novel Bruton's tyrosine kinase mutations in 10 unrelated subjects with X linked agammaglobulinaemia.
Brooimans RA; van den Berg AJ; Rijkers GT; Sanders LA; van Amstel JK; Tilanus MG; Grubben MJ; Zegers BJ
J Med Genet; 1997 Jun; 34(6):484-8. PubMed ID: 9192269
[TBL] [Abstract][Full Text] [Related]
26. [A retrospective study of one case of X-linked agammaglobulinemia].
Li DX; Wang XC; Tan SY; Lao SH; Chen ZH; Wang YH; Li FZ; Liang YQ; Wang J
Zhonghua Jie He He Hu Xi Za Zhi; 2006 Dec; 29(12):796-800. PubMed ID: 17327079
[TBL] [Abstract][Full Text] [Related]
27. Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivation.
Takada H; Kanegane H; Nomura A; Yamamoto K; Ihara K; Takahashi Y; Tsukada S; Miyawaki T; Hara T
Blood; 2004 Jan; 103(1):185-7. PubMed ID: 12958074
[TBL] [Abstract][Full Text] [Related]
28. Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry.
Kanegane H; Tsukada S; Iwata T; Futatani T; Nomura K; Yamamoto J; Yoshida T; Agematsu K; Komiyama A; Miyawaki T
Clin Exp Immunol; 2000 Jun; 120(3):512-7. PubMed ID: 10844531
[TBL] [Abstract][Full Text] [Related]
29. Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia.
Wang Y; Kanegane H; Sanal O; Ersoy F; Tezcan I; Futatani T; Tsukada S; Miyawaki T
Hum Mutat; 2001 Oct; 18(4):356. PubMed ID: 11668622
[TBL] [Abstract][Full Text] [Related]
30. Characterization of mutations, including a novel regulatory defect in the first intron, in Bruton's tyrosine kinase gene from seven Korean X-linked agammaglobulinemia families.
Jo EK; Kanegane H; Nonoyama S; Tsukada S; Lee JH; Lim K; Shong M; Song CH; Kim HJ; Park JK; Miyawaki T
J Immunol; 2001 Oct; 167(7):4038-45. PubMed ID: 11564824
[TBL] [Abstract][Full Text] [Related]
31. Delayed diagnosis of X-linked agammaglobulinaemia in a boy with recurrent meningitis.
Zhang YN; Gao YY; Yang SD; Cao BB; Zheng KL; Wei P; Chen LF; Chen WX
BMC Neurol; 2019 Dec; 19(1):320. PubMed ID: 31830942
[TBL] [Abstract][Full Text] [Related]
32. Identification of mutations of Bruton's tyrosine kinase gene (BTK) in Brazilian patients with X-linked agammaglobulinemia.
Tani SM; Wang Y; Kanegane H; Futatani T; Pinto J; Vilela MM; Miyawaki T
Hum Mutat; 2002 Sep; 20(3):235-6. PubMed ID: 12204007
[TBL] [Abstract][Full Text] [Related]
33. Detection of a novel mutation in the SRC homology domain 2 (SH2) of Bruton's tyrosine kinase and direct female carrier evaluation in a family with X-linked agammaglobulinemia.
Schuster V; Seidenspinner S; Kreth HW
Am J Med Genet; 1996 May; 63(1):318-22. PubMed ID: 8723128
[TBL] [Abstract][Full Text] [Related]
34. Characterization of germline mutations of the gene encoding Bruton's tyrosine kinase in families with X-linked agammaglobulinemia.
Hagemann TL; Rosen FS; Kwan SP
Hum Mutat; 1995; 5(4):296-302. PubMed ID: 7627183
[TBL] [Abstract][Full Text] [Related]
35. Composition of precursor B-cell compartment in bone marrow from patients with X-linked agammaglobulinemia compared with healthy children.
Noordzij JG; de Bruin-Versteeg S; Comans-Bitter WM; Hartwig NG; Hendriks RW; de Groot R; van Dongen JJ
Pediatr Res; 2002 Feb; 51(2):159-68. PubMed ID: 11809909
[TBL] [Abstract][Full Text] [Related]
36. A novel Bruton's tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia.
Zheng B; Zhang Y; Jin Y; Yu H
BMC Pediatr; 2014 Oct; 14():265. PubMed ID: 25316352
[TBL] [Abstract][Full Text] [Related]
37. De novo mutation in the BTK gene of atypical X-linked agammaglobulinemia in a patient with recurrent pyoderma.
Lin MT; Chien YH; Shyur SD; Huang LH; Chiang YC; Wen DC; Liang PH; Yang HC
Ann Allergy Asthma Immunol; 2006 May; 96(5):744-8. PubMed ID: 16729790
[TBL] [Abstract][Full Text] [Related]
38. Identification of nine novel mutations in the Bruton's tyrosine kinase gene in X-linked agammaglobulinaemia patients.
Orlandi P; Ritis K; Moschese V; Angelini F; Arvanitidis K; Speletas M; Sideras P; Plebani A; Rossi P
Hum Mutat; 2000 Jan; 15(1):117. PubMed ID: 10612838
[TBL] [Abstract][Full Text] [Related]
39. Twin carriers of X-linked agammaglobulinemia (XLA) due to germline mutation in the Btk gene.
Curtis SK; Hebert MD; Saha BK
Am J Med Genet; 2000 Jan; 90(3):229-32. PubMed ID: 10678660
[TBL] [Abstract][Full Text] [Related]
40. Kinase mutant Btk results in atypical X-linked agammaglobulinaemia phenotype.
Gaspar HB; Ferrando M; Caragol I; Hernandez M; Bertran JM; De Gracia X; Lester T; Kinnon C; Ashton E; Espanol T
Clin Exp Immunol; 2000 May; 120(2):346-50. PubMed ID: 10792386
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
