Holtgreve-Grez H - Search Results

1

Genetic characterization of a human skin carcinoma progression model: from primary tumor to metastasis.

Popp S, Waltering S, Holtgreve-Grez H, Jauch A, Proby C, Leigh IM, Boukamp P. Popp S, et al. J Invest Dermatol. 2000 Dec;115(6):1095-103. doi: 10.1046/j.1523-1747.2000.00173.x. J Invest Dermatol. 2000. PMID: 11121147 Free article.

2

Comparison of DNA gains and losses in primary renal clear cell carcinomas and metastatic sites: importance of 1q and 3p copy number changes in metastatic events.

Gronwald J, Störkel S, Holtgreve-Grez H, Hadaczek P, Brinkschmidt C, Jauch A, Lubinski J, Cremer T. Gronwald J, et al. Cancer Res. 1997 Feb 1;57(3):481-7. Cancer Res. 1997. PMID: 9012478

3

Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics.

Granzow M, Popp S, Weber S, Schoell B, Holtgreve-Grez H, Senf L, Hager D, Boschert J, Scheurlen W, Jauch A. Granzow M, et al. Cancer Genet Cytogenet. 2001 Oct 1;130(1):79-83. doi: 10.1016/s0165-4608(01)00465-4. Cancer Genet Cytogenet. 2001. PMID: 11672779

4

The telomere profile distinguishes two classes of genetically distinct cutaneous squamous cell carcinomas.

Leufke C, Leykauf J, Krunic D, Jauch A, Holtgreve-Grez H, Böhm-Steuer B, Bröcker EB, Mauch C, Utikal J, Hartschuh W, Purdie KJ, Boukamp P. Leufke C, et al. Among authors: holtgreve grez h. Oncogene. 2014 Jul 3;33(27):3506-18. doi: 10.1038/onc.2013.323. Epub 2013 Aug 19. Oncogene. 2014. PMID: 23955078

5

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.

Popp S, Schulze B, Granzow M, Keller M, Holtgreve-Grez H, Schoell B, Brough M, Hager HD, Tariverdian G, Brown J, Kearney L, Jauch A. Popp S, et al. Among authors: holtgreve grez h. Hum Genet. 2002 Jul;111(1):31-9. doi: 10.1007/s00439-002-0739-x. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136233

6

Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals.

Granzow M, Popp S, Keller M, Holtgreve-Grez H, Brough M, Schoell B, Rauterberg-Ruland I, Hager HD, Tariverdian G, Jauch A. Granzow M, et al. Hum Genet. 2000 Jul;107(1):51-7. doi: 10.1007/s004390000321. Hum Genet. 2000. PMID: 10982035

7

Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis.

Scholz I, Popp S, Granzow M, Schoell B, Holtgreve-Grez H, Takeuchi S, Schrappe M, Harbott J, Teigler-Schlegel A, Zimmermann M, Fischer C, Koeffler HP, Bartram CR, Jauch A. Scholz I, et al. Cancer Genet Cytogenet. 2001 Jan 15;124(2):89-97. doi: 10.1016/s0165-4608(00)00330-7. Cancer Genet Cytogenet. 2001. PMID: 11172898

8

Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.

Joos S, Granzow M, Holtgreve-Grez H, Siebert R, Harder L, Martín-Subero JI, Wolf J, Adamowicz M, Barth TF, Lichter P, Jauch A. Joos S, et al. Among authors: holtgreve grez h. Int J Cancer. 2003 Feb 10;103(4):489-95. doi: 10.1002/ijc.10845. Int J Cancer. 2003. PMID: 12478664

9

Chromosomal abnormalities in renal cell neoplasms associated with acquired renal cystic disease. A series studied by comparative genomic hybridization and fluorescence in situ hybridization.

Gronwald J, Baur AS, Holtgreve-Grez H, Jauch A, Mosimann F, Jichlinski P, Wauters JP, Cremer T, Guillou L. Gronwald J, et al. J Pathol. 1999 Feb;187(3):308-12. doi: 10.1002/(SICI)1096-9896(199902)187:3<308::AID-PATH256>3.0.CO;2-E. J Pathol. 1999. PMID: 10398084

10

Separate and variably shaped chromosome arm domains are disclosed by chromosome arm painting in human cell nuclei.

Dietzel S, Jauch A, Kienle D, Qu G, Holtgreve-Grez H, Eils R, Münkel C, Bittner M, Meltzer PS, Trent JM, Cremer T. Dietzel S, et al. Chromosome Res. 1998 Jan;6(1):25-33. doi: 10.1023/a:1009262223693. Chromosome Res. 1998. PMID: 9510507

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