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Items: 1 to 20 of 24

1.

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses.

Ou Z, Kang SH, Shaw CA, Carmack CE, White LD, Patel A, Beaudet AL, Cheung SW, Chinault AC.

Genet Med. 2008 Apr;10(4):278-89. doi: 10.1097/GIM.0b013e31816b4420.

2.

HOX gene regulation in acute myeloid leukemia: CDX marks the spot?

Fröhling S, Scholl C, Bansal D, Huntly BJ.

Cell Cycle. 2007 Sep 15;6(18):2241-5. Epub 2007 Jun 29. Review.

PMID:
17881901
3.

Trisomy of chromosome 21 in leukemogenesis.

Izraeli S, Rainis L, Hertzberg L, Smooha G, Birger Y.

Blood Cells Mol Dis. 2007 Sep-Oct;39(2):156-9. Epub 2007 May 29. Review.

PMID:
17532652
4.

Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.

Matheny CJ, Speck ME, Cushing PR, Zhou Y, Corpora T, Regan M, Newman M, Roudaia L, Speck CL, Gu TL, Griffey SM, Bushweller JH, Speck NA.

EMBO J. 2007 Feb 21;26(4):1163-75. Epub 2007 Feb 8.

5.

Hematological abnormalities during the first week of life among neonates with Down syndrome: data from a multihospital healthcare system.

Henry E, Walker D, Wiedmeier SE, Christensen RD.

Am J Med Genet A. 2007 Jan 1;143A(1):42-50.

PMID:
17163522
6.

Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21.

Strefford JC, van Delft FW, Robinson HM, Worley H, Yiannikouris O, Selzer R, Richmond T, Hann I, Bellotti T, Raghavan M, Young BD, Saha V, Harrison CJ.

Proc Natl Acad Sci U S A. 2006 May 23;103(21):8167-72. Epub 2006 May 15.

7.

Deletion of chromosome 21 disturbs human brain morphogenesis.

Yao G, Chen XN, Flores-Sarnat L, Barlow GM, Palka G, Moeschler JB, McGillivray B, Morse RP, Korenberg JR.

Genet Med. 2006 Jan;8(1):1-7.

PMID:
16418593
8.

Development and validation of a CGH microarray for clinical cytogenetic diagnosis.

Cheung SW, Shaw CA, Yu W, Li J, Ou Z, Patel A, Yatsenko SA, Cooper ML, Furman P, Stankiewicz P, Lupski JR, Chinault AC, Beaudet AL.

Genet Med. 2005 Jul-Aug;7(6):422-32. Erratum in: Genet Med. 2005 Sep;7(7):478. Stankiewicz, Pawal [corrected to Stankiewicz, Pawel].

PMID:
16024975
9.

HOXB6 overexpression in murine bone marrow immortalizes a myelomonocytic precursor in vitro and causes hematopoietic stem cell expansion and acute myeloid leukemia in vivo.

Fischbach NA, Rozenfeld S, Shen W, Fong S, Chrobak D, Ginzinger D, Kogan SC, Radhakrishnan A, Le Beau MM, Largman C, Lawrence HJ.

Blood. 2005 Feb 15;105(4):1456-66. Epub 2004 Nov 2.

11.

Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia.

Osato M.

Oncogene. 2004 May 24;23(24):4284-96. Review.

PMID:
15156185
12.

High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia.

Harada H, Harada Y, Niimi H, Kyo T, Kimura A, Inaba T.

Blood. 2004 Mar 15;103(6):2316-24. Epub 2003 Nov 13.

13.

Inherited thrombocytopenias: from genes to therapy.

Balduini CL, Iolascon A, Savoia A.

Haematologica. 2002 Aug;87(8):860-80. Review.

14.

Risks of leukaemia and solid tumours in individuals with Down's syndrome.

Hasle H, Clemmensen IH, Mikkelsen M.

Lancet. 2000 Jan 15;355(9199):165-9.

PMID:
10675114
15.

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.

Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D, Ratajczak J, Resende IC, Haworth C, Hock R, Loh M, Felix C, Roy DC, Busque L, Kurnit D, Willman C, Gewirtz AM, Speck NA, Bushweller JH, Li FP, Gardiner K, Poncz M, Maris JM, Gilliland DG.

Nat Genet. 1999 Oct;23(2):166-75.

PMID:
10508512
16.

Molecular genetics of childhood leukemias.

Rubnitz JE, Look AT.

J Pediatr Hematol Oncol. 1998 Jan-Feb;20(1):1-11.

PMID:
9482406
17.

Mutations in the hminK gene cause long QT syndrome and suppress IKs function.

Splawski I, Tristani-Firouzi M, Lehmann MH, Sanguinetti MC, Keating MT.

Nat Genet. 1997 Nov;17(3):338-40.

PMID:
9354802
18.

KCNE1 mutations cause jervell and Lange-Nielsen syndrome.

Schulze-Bahr E, Wang Q, Wedekind H, Haverkamp W, Chen Q, Sun Y, Rubie C, Hördt M, Towbin JA, Borggrefe M, Assmann G, Qu X, Somberg JC, Breithardt G, Oberti C, Funke H.

Nat Genet. 1997 Nov;17(3):267-8. No abstract available.

PMID:
9354783
19.

Oncogenic transcription factors in the human acute leukemias.

Look AT.

Science. 1997 Nov 7;278(5340):1059-64. Review.

PMID:
9353180
20.

Acute lymphoblastic leukemia and chromosome 21.

Berger R.

Cancer Genet Cytogenet. 1997 Mar;94(1):8-12. Review.

PMID:
9078285

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