Schoch C - Search Results

1

Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease.

Tartaglia M, Martinelli S, Stella L, Bocchinfuso G, Flex E, Cordeddu V, Zampino G, Burgt Iv, Palleschi A, Petrucci TC, Sorcini M, Schoch C, Foa R, Emanuel PD, Gelb BD. Tartaglia M, et al. Among authors: schoch c. Am J Hum Genet. 2006 Feb;78(2):279-90. doi: 10.1086/499925. Epub 2005 Dec 7. Am J Hum Genet. 2006. PMID: 16358218 Free PMC article.

2

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.

Storlazzi CT, Fioretos T, Surace C, Lonoce A, Mastrorilli A, Strömbeck B, D'Addabbo P, Iacovelli F, Minervini C, Aventin A, Dastugue N, Fonatsch C, Hagemeijer A, Jotterand M, Mühlematter D, Lafage-Pochitaloff M, Nguyen-Khac F, Schoch C, Slovak ML, Smith A, Solè F, Van Roy N, Johansson B, Rocchi M. Storlazzi CT, et al. Among authors: schoch c. Hum Mol Genet. 2006 Mar 15;15(6):933-42. doi: 10.1093/hmg/ddl010. Epub 2006 Feb 1. Hum Mol Genet. 2006. PMID: 16452126

3

Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies.

Poppe B, Vandesompele J, Schoch C, Lindvall C, Mrozek K, Bloomfield CD, Beverloo HB, Michaux L, Dastugue N, Herens C, Yigit N, De Paepe A, Hagemeijer A, Speleman F. Poppe B, et al. Among authors: schoch c. Blood. 2004 Jan 1;103(1):229-35. doi: 10.1182/blood-2003-06-2163. Epub 2003 Aug 28. Blood. 2004. PMID: 12946992 Free article.

4

GAB2 is a novel target of 11q amplification in AML/MDS.

Zatkova A, Schoch C, Speleman F, Poppe B, Mannhalter C, Fonatsch C, Wimmer K. Zatkova A, et al. Among authors: schoch c. Genes Chromosomes Cancer. 2006 Sep;45(9):798-807. doi: 10.1002/gcc.20344. Genes Chromosomes Cancer. 2006. PMID: 16736498

5

Fluorescence in situ hybridization characterization of the chromosomal breakpoints in a case with ins(17;3)(q11.2;q21q26.3) and acute monocytic leukemia.

Schnittger S, Joachimmayer E, Schoch C, Fuchs R, Fonatsch C. Schnittger S, et al. Among authors: schoch c. Cancer Genet Cytogenet. 1998 Oct 15;106(2):122-7. doi: 10.1016/s0165-4608(98)00071-5. Cancer Genet Cytogenet. 1998. PMID: 9797776

6

21q22 balanced chromosome aberrations in therapy-related hematopoietic disorders: report from an international workshop.

Slovak ML, Bedell V, Popplewell L, Arber DA, Schoch C, Slater R. Slovak ML, et al. Among authors: schoch c. Genes Chromosomes Cancer. 2002 Apr;33(4):379-94. doi: 10.1002/gcc.10042. Genes Chromosomes Cancer. 2002. PMID: 11921272

7

Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients.

Zatkova A, Ullmann R, Rouillard JM, Lamb BJ, Kuick R, Hanash SM, Schnittger S, Schoch C, Fonatsch C, Wimmer K. Zatkova A, et al. Among authors: schoch c. Genes Chromosomes Cancer. 2004 Apr;39(4):263-76. doi: 10.1002/gcc.20002. Genes Chromosomes Cancer. 2004. PMID: 14978788

8

Computer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notation.

Bradtke J, Balz H, Fonatsch C, Heinze B, Jauch A, Mohr B, Schoch C, Rieder H. Bradtke J, et al. Among authors: schoch c. BMC Bioinformatics. 2003 Jan 28;4:4. doi: 10.1186/1471-2105-4-4. Epub 2003 Jan 28. BMC Bioinformatics. 2003. PMID: 12549981 Free PMC article.

9

Increased risk for therapy-associated hematologic malignancies in patients with carcinoma of the breast and combined homozygous gene deletions of glutathione transferases M1 and T1.

Haase D, Binder C, Bünger J, Fonatsch C, Streubel B, Schnittger S, Griesinger F, Westphal G, Schoch C, Knopp A, Berkovicz D, Krieger O, Wörmann B, Hilgers R, Hallier E, Schulz T. Haase D, et al. Among authors: schoch c. Leuk Res. 2002 Mar;26(3):249-54. doi: 10.1016/s0145-2126(01)00124-2. Leuk Res. 2002. PMID: 11792413

10

A case of atypical myelodysplastic syndrome with micromegakaryocytes, normal platelet count, and t(3;12)(q21;p13) with inv(3)(q21q26).

Schnittger S, Schoch C, Streubel B, Hinrichs HF, Otremba B, Parwaresch R, Fonatsch C. Schnittger S, et al. Among authors: schoch c. Genes Chromosomes Cancer. 1997 Nov;20(3):292-8. Genes Chromosomes Cancer. 1997. PMID: 9365837

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