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Items: 1 to 20 of 52

1.

Agammaglobulinemia.

BRUTON OC.

Pediatrics. 1952 Jun;9(6):722-8. No abstract available.

PMID:
14929630
2.
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4.

Flow cytometric analysis of Wiskott-Aldrich syndrome (WAS) protein in lymphocytes from WAS patients and their familial carriers.

Yamada M, Ohtsu M, Kobayashi I, Kawamura N, Kobayashi K, Ariga T, Sakiyama Y, Nelson DL, Tsuruta S, Anakura M, Ishikawa N.

Blood. 1999 Jan 15;93(2):756-7. No abstract available.

5.

Waltzing with WASP.

Ramesh N, Antón IM, Martínez-Quiles N, Geha RS.

Trends Cell Biol. 1999 Jan;9(1):15-9. Review.

PMID:
10087612
6.

Intrinsic dendritic cell abnormalities in Wiskott-Aldrich syndrome.

Binks M, Jones GE, Brickell PM, Kinnon C, Katz DR, Thrasher AJ.

Eur J Immunol. 1998 Oct;28(10):3259-67.

7.

The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM.

Sayos J, Wu C, Morra M, Wang N, Zhang X, Allen D, van Schaik S, Notarangelo L, Geha R, Roncarolo MG, Oettgen H, De Vries JE, Aversa G, Terhorst C.

Nature. 1998 Oct 1;395(6701):462-9.

PMID:
9774102
8.

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene.

Coffey AJ, Brooksbank RA, Brandau O, Oohashi T, Howell GR, Bye JM, Cahn AP, Durham J, Heath P, Wray P, Pavitt R, Wilkinson J, Leversha M, Huckle E, Shaw-Smith CJ, Dunham A, Rhodes S, Schuster V, Porta G, Yin L, Serafini P, Sylla B, Zollo M, Franco B, Bolino A, Seri M, Lanyi A, Davis JR, Webster D, Harris A, Lenoir G, de St Basile G, Jones A, Behloradsky BH, Achatz H, Murken J, Fassler R, Sumegi J, Romeo G, Vaudin M, Ross MT, Meindl A, Bentley DR.

Nat Genet. 1998 Oct;20(2):129-35.

PMID:
9771704
9.

Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients.

MacCarthy-Morrogh L, Gaspar HB, Wang YC, Katz F, Thompson L, Layton M, Jones AM, Kinnon C.

Clin Immunol Immunopathol. 1998 Jul;88(1):22-7.

PMID:
9683546
10.

Chemotaxis of macrophages is abolished in the Wiskott-Aldrich syndrome.

Zicha D, Allen WE, Brickell PM, Kinnon C, Dunn GA, Jones GE, Thrasher AJ.

Br J Haematol. 1998 Jun;101(4):659-65.

PMID:
9674738
11.

T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates.

Kohn DB, Hershfield MS, Carbonaro D, Shigeoka A, Brooks J, Smogorzewska EM, Barsky LW, Chan R, Burotto F, Annett G, Nolta JA, Crooks G, Kapoor N, Elder M, Wara D, Bowen T, Madsen E, Snyder FF, Bastian J, Muul L, Blaese RM, Weinberg K, Parkman R.

Nat Med. 1998 Jul;4(7):775-80.

13.

Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection.

Futatani T, Miyawaki T, Tsukada S, Hashimoto S, Kunikata T, Arai S, Kurimoto M, Niida Y, Matsuoka H, Sakiyama Y, Iwata T, Tsuchiya S, Tatsuzawa O, Yoshizaki K, Kishimoto T.

Blood. 1998 Jan 15;91(2):595-602.

14.

Restoration of lymphocyte function in Janus kinase 3-deficient mice by retroviral-mediated gene transfer.

Bunting KD, Sangster MY, Ihle JN, Sorrentino BP.

Nat Med. 1998 Jan;4(1):58-64.

PMID:
9427607
15.

Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia.

Minegishi Y, Coustan-Smith E, Wang YH, Cooper MD, Campana D, Conley ME.

J Exp Med. 1998 Jan 5;187(1):71-7.

16.
17.

Defective antigen-induced lymphocyte proliferation in the X-linked hyper-IgM syndrome.

Ameratunga R, Lederman HM, Sullivan KE, Ochs HD, Seyama K, French JK, Prestidge R, Marbrook J, Fanslow WC, Winkelstein JA.

J Pediatr. 1997 Jul;131(1 Pt 1):147-50.

PMID:
9255207
18.

Clinical spectrum of X-linked hyper-IgM syndrome.

Levy J, Espanol-Boren T, Thomas C, Fischer A, Tovo P, Bordigoni P, Resnick I, Fasth A, Baer M, Gomez L, Sanders EA, Tabone MD, Plantaz D, Etzioni A, Monafo V, Abinun M, Hammarstrom L, Abrahamsen T, Jones A, Finn A, Klemola T, DeVries E, Sanal O, Peitsch MC, Notarangelo LD.

J Pediatr. 1997 Jul;131(1 Pt 1):47-54.

PMID:
9255191
19.

Molecular mechanisms in B cell antigen receptor signaling.

Kurosaki T.

Curr Opin Immunol. 1997 Jun;9(3):309-18. Review.

PMID:
9203415
20.

Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency.

Puck JM, Pepper AE, Henthorn PS, Candotti F, Isakov J, Whitwam T, Conley ME, Fischer RE, Rosenblatt HM, Small TN, Buckley RH.

Blood. 1997 Mar 15;89(6):1968-77.

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