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Items: 12

1.

Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies.

Stephens K, Weaver M, Leppig KA, Maruyama K, Emanuel PD, Le Beau MM, Shannon KM.

Blood. 2006 Sep 1;108(5):1684-9. Epub 2006 May 11.

2.

Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis.

Shannon KM, Watterson J, Johnson P, O'Connell P, Lange B, Shah N, Steinherz P, Kan YW, Priest JR.

Blood. 1992 Mar 1;79(5):1311-8. Review.

3.
4.

The NF1 translocation breakpoint region.

O'Connell P, Cawthon RM, Viskochil D, White R, Carey JC, Buchberg AM.

Ann N Y Acad Sci. 1991;615:319-31. Review.

PMID:
1903909
5.

A late onset sickle cell disease reveals a mosaic segmental uniparental isodisomy of chromosome 11p15.

Vinatier I, Martin X, Costa JM, Bazin A, Giraudier S, Joly P.

Blood Cells Mol Dis. 2015 Jan;54(1):53-5. doi: 10.1016/j.bcmd.2014.07.021. Epub 2014 Aug 20. Review.

PMID:
25159120
6.

[Deletion of the long arm of chromosome 5 in patients with hematologic malignancies].

Brezinová J, Zemanová Z, Michalová K.

Cas Lek Cesk. 2001 Feb 1;140(2):43-6. Review. Czech.

PMID:
11262906
7.

Inherited predispositions and hyperactive Ras in myeloid leukemogenesis.

Lauchle JO, Braun BS, Loh ML, Shannon K.

Pediatr Blood Cancer. 2006 May 1;46(5):579-85. Review.

PMID:
16261595
8.

Modeling myeloid leukemia tumor suppressor gene inactivation in the mouse.

Shannon KM, Le Beau MM, Largaespada DA, Killeen N.

Semin Cancer Biol. 2001 Jun;11(3):191-200. Review.

PMID:
11407944
9.

Pathogenesis and consequences of uniparental disomy in cancer.

Makishima H, Maciejewski JP.

Clin Cancer Res. 2011 Jun 15;17(12):3913-23. doi: 10.1158/1078-0432.CCR-10-2900. Epub 2011 Apr 25. Review.

10.

Genetic and molecular genetic studies in the diagnosis of myeloid diseases.

Anastasi J.

Hum Pathol. 2003 Apr;34(4):306-13. Review. No abstract available.

PMID:
12733108
11.

The neurofibromatosis type 1 (NF1) tumor suppressor gene and myeloid leukemia.

Largaespada DA, Brannan CI, Shaughnessy JD, Jenkins NA, Copeland NG.

Curr Top Microbiol Immunol. 1996;211:233-9. Review. No abstract available.

PMID:
8585954
12.

Uniparental disomy.

Siegel DH, Slavotinek A.

Pediatr Dermatol. 2005 Sep-Oct;22(5):482-7. Review. No abstract available. Erratum in: Pediatr Dermatol. 2005 Nov-Dec;22(6):589-90.

PMID:
16191008
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