Hoehn H - Search Results

1

Variable response to the diepoxybutane test in two dizygotic twins with Fanconi's anemia and flow cytometry for diagnosis confirmation.

Toraldo R, Canino G, Tolone C, D'Avanzo M, Porfirio B, Hoehn H, Schroeder-Kurth T, Pistoia V. Toraldo R, et al. Among authors: hoehn h. Pediatr Hematol Oncol. 1998 Jan-Feb;15(1):45-54. doi: 10.3109/08880019809009507. Pediatr Hematol Oncol. 1998. PMID: 9509505

2

Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia.

Seyschab H, Friedl R, Sun Y, Schindler D, Hoehn H, Hentze S, Schroeder-Kurth T. Seyschab H, et al. Among authors: hoehn h. Blood. 1995 Apr 15;85(8):2233-7. Blood. 1995. PMID: 7718895 Free article.

3

Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1Q12-32 triplication) via BrdU/Hoechst flow cytometry.

Schindler D, Kubbies M, Hoehn H, Schinzel A, Rabinovitch PS. Schindler D, et al. Among authors: hoehn h. Am J Pediatr Hematol Oncol. 1987 Summer;9(2):172-7. doi: 10.1097/00043426-198722000-00014. Am J Pediatr Hematol Oncol. 1987. PMID: 3592130

4

Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot study.

Bechtold A, Friedl R, Kalb R, Gottwald B, Neveling K, Gavvovidis I, Herterich S, Schindler D, Hoehn H. Bechtold A, et al. Among authors: hoehn h. Fetal Diagn Ther. 2006;21(1):118-24. doi: 10.1159/000089061. Fetal Diagn Ther. 2006. PMID: 16354989

5

Cell cycle effects of the DNA topoisomerase inhibitors camptothecin and m-AMSA in lymphoblastoid cell lines from patients with Fanconi anemia.

Poot M, Epe B, Hoehn H. Poot M, et al. Among authors: hoehn h. Mutat Res. 1992 Nov 16;270(2):185-9. doi: 10.1016/0027-5107(92)90129-p. Mutat Res. 1992. PMID: 1383735

6

Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells.

Kubbies M, Schindler D, Hoehn H, Schinzel A, Rabinovitch PS. Kubbies M, et al. Among authors: hoehn h. Am J Hum Genet. 1985 Sep;37(5):1022-30. Am J Hum Genet. 1985. PMID: 4050789 Free PMC article.

7

Confounding factors in the diagnosis of Fanconi anaemia.

Joenje H, Arwert F, Kwee ML, Madan K, Hoehn H. Joenje H, et al. Among authors: hoehn h. Am J Med Genet. 1998 Oct 12;79(5):403-5. doi: 10.1002/(sici)1096-8628(19981012)79:5<403::aid-ajmg16>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9779812 No abstract available.

8

Localisation of a Fanconi anaemia gene to chromosome 9p.

Saar K, Schindler D, Wegner RD, Reis A, Wienker TF, Hoehn H, Joenje H, Sperling K, Digweed M. Saar K, et al. Among authors: hoehn h. Eur J Hum Genet. 1998 Sep-Oct;6(5):501-8. doi: 10.1038/sj.ejhg.5200241. Eur J Hum Genet. 1998. PMID: 9801875

9

Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.

Gross M, Hanenberg H, Lobitz S, Friedl R, Herterich S, Dietrich R, Gruhn B, Schindler D, Hoehn H. Gross M, et al. Among authors: hoehn h. Cytogenet Genome Res. 2002;98(2-3):126-35. doi: 10.1159/000069805. Cytogenet Genome Res. 2002. PMID: 12697994

10

Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay.

Djuzenova CS, Rothfuss A, Oppitz U, Spelt G, Schindler D, Hoehn H, Flentje M. Djuzenova CS, et al. Among authors: hoehn h. Lab Invest. 2001 Feb;81(2):185-92. doi: 10.1038/labinvest.3780226. Lab Invest. 2001. PMID: 11232640 Free article.

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