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Items: 19


Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP.

Palendira U, Low C, Chan A, Hislop AD, Ho E, Phan TG, Deenick E, Cook MC, Riminton DS, Choo S, Loh R, Alvaro F, Booth C, Gaspar HB, Moretta A, Khanna R, Rickinson AB, Tangye SG.

PLoS Biol. 2011 Nov;9(11):e1001187. doi: 10.1371/journal.pbio.1001187. Epub 2011 Nov 1.


Hematopoiesis is not clonal in healthy elderly women.

Swierczek SI, Agarwal N, Nussenzveig RH, Rothstein G, Wilson A, Artz A, Prchal JT.

Blood. 2008 Oct 15;112(8):3186-93. doi: 10.1182/blood-2008-03-143925. Epub 2008 Jul 18.


X-linked clonality testing: interpretation and limitations.

Chen GL, Prchal JT.

Blood. 2007 Sep 1;110(5):1411-9. Epub 2007 Apr 13. Review.


Antigen receptor-induced activation and cytoskeletal rearrangement are impaired in Wiskott-Aldrich syndrome protein-deficient lymphocytes.

Zhang J, Shehabeldin A, da Cruz LA, Butler J, Somani AK, McGavin M, Kozieradzki I, dos Santos AO, Nagy A, Grinstein S, Penninger JM, Siminovitch KA.

J Exp Med. 1999 Nov 1;190(9):1329-42.


An X chromosome gene regulates hematopoietic stem cell kinetics.

Abkowitz JL, Taboada M, Shelton GH, Catlin SN, Guttorp P, Kiklevich JV.

Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3862-6.


Clonal hematopoiesis and acquired thalassemia in common variable immunodeficiency.

Belickova M, Schroeder HW Jr, Guan YL, Brierre J, Berney S, Cooper MD, Prchal JT.

Mol Med. 1994 Nov;1(1):56-61.


Linkage studies in carriers of Lowe oculo-cerebro-renal syndrome.

Hittner HM, Carroll AJ, Prchal JT.

Am J Hum Genet. 1982 Nov;34(6):966-71.


Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

Migeon BR, Moser HW, Moser AB, Axelman J, Sillence D, Norum RA.

Proc Natl Acad Sci U S A. 1981 Aug;78(8):5066-70.


Unbalanced X chromosome mosaicism in B cells of mice with X-linked immunodeficiency.

Nahm MH, Paslay JW, Davie JM.

J Exp Med. 1983 Sep 1;158(3):920-31.


Treatment of acute myeloid leukemia cells in vitro with a monoclonal antibody recognizing a myeloid differentiation antigen allows normal progenitor cells to be expressed.

Bernstein ID, Singer JW, Andrews RG, Keating A, Powell JS, Bjornson BH, Cuttner J, Najfeld V, Reaman G, Raskind W, et al.

J Clin Invest. 1987 Apr;79(4):1153-9.


Selection against lethal alleles in females heterozygous for incontinentia pigmenti.

Migeon BR, Axelman J, Jan de Beur S, Valle D, Mitchell GA, Rosenbaum KN.

Am J Hum Genet. 1989 Jan;44(1):100-6.


Genetics of human X-linked immunodeficiency diseases.

Hendriks RW, Schuurman RK.

Clin Exp Immunol. 1991 Aug;85(2):182-92. Review. No abstract available.


Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus.

Hendriks RW, De Weers M, Mensink RG, Kraakman ME, Mollee-Versteegde IF, Veerman AJ, Sandkuyl LA, Schuurman RK.

Clin Exp Immunol. 1991 May;84(2):219-22.


Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl.

Clarke JT, Greer WL, Strasberg PM, Pearce RD, Skomorowski MA, Ray PN.

Am J Hum Genet. 1991 Aug;49(2):289-97.


Evidence for defective transmembrane signaling in B cells from patients with Wiskott-Aldrich syndrome.

Simon HU, Mills GB, Hashimoto S, Siminovitch KA.

J Clin Invest. 1992 Oct;90(4):1396-405.

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