Wöhr G - Search Results

1

Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43.

Berthon P, Valeri A, Cohen-Akenine A, Drelon E, Paiss T, Wöhr G, Latil A, Millasseau P, Mellah I, Cohen N, Blanché H, Bellané-Chantelot C, Demenais F, Teillac P, Le Duc A, de Petriconi R, Hautmann R, Chumakov I, Bachner L, Maitland NJ, Lidereau R, Vogel W, Fournier G, Mangin P, Cussenot O, et al. Berthon P, et al. Among authors: wohr g. Am J Hum Genet. 1998 Jun;62(6):1416-24. doi: 10.1086/301879. Am J Hum Genet. 1998. PMID: 9585607 Free PMC article.

2

(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French-German population.

Correa-Cerro L, Wöhr G, Häussler J, Berthon P, Drelon E, Mangin P, Fournier G, Cussenot O, Kraus P, Just W, Paiss T, Cantú JM, Vogel W. Correa-Cerro L, et al. Among authors: wohr g. Eur J Hum Genet. 1999 Apr;7(3):357-62. doi: 10.1038/sj.ejhg.5200298. Eur J Hum Genet. 1999. PMID: 10234512

3

Chromosomal changes during progression of transitional cell carcinoma of the bladder and delineation of the amplified interval on chromosome arm 8q.

Bruch J, Wöhr G, Hautmann R, Mattfeldt T, Brüderlein S, Möller P, Sauter S, Hameister H, Vogel W, Paiss T. Bruch J, et al. Among authors: wohr g. Genes Chromosomes Cancer. 1998 Oct;23(2):167-74. doi: 10.1002/(sici)1098-2264(199810)23:2<167::aid-gcc10>3.0.co;2-l. Genes Chromosomes Cancer. 1998. PMID: 9739020

4

Detailed marker chromosome analysis in cell line U-BLC1, established from transitional-cell carcinoma of the bladder.

Bruch J, Wöhr G, Brüderlein S, Barbi G, Wolter H, Dixkens C, Mattfeldt T, Möller P, Paiss T, Hautmann R, Vogel W, Hameister H. Bruch J, et al. Among authors: wohr g. Int J Cancer. 1999 Mar 15;80(6):903-10. doi: 10.1002/(sici)1097-0215(19990315)80:6<903::aid-ijc17>3.0.co;2-8. Int J Cancer. 1999. PMID: 10074925

5

Some tumors of the bladder are polyclonal in origin.

Paiss T, Wöhr G, Hautmann RE, Mattfeldt T, Müller M, Haeussler J, Vogel W. Paiss T, et al. Among authors: wohr g. J Urol. 2002 Feb;167(2 Pt 1):718-23. doi: 10.1016/S0022-5347(01)69133-X. J Urol. 2002. PMID: 11792960

6

Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype.

Barbi G, Kennerknecht I, Wöhr G, Avramopoulos D, Karadima G, Petersen MB. Barbi G, et al. Among authors: wohr g. Am J Med Genet. 2000 Mar 13;91(2):116-22. doi: 10.1002/(sici)1096-8628(20000313)91:2<116::aid-ajmg7>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10748409

7

Mapping of members of the low-copy-number repetitive DNA sequence family chAB4 within the p arms of human acrocentric chromosomes: characterization of Robertsonian translocations.

Kehrer-Sawatzki H, Wöhr G, Schempp W, Eisenbarth I, Barbi G, Assum G. Kehrer-Sawatzki H, et al. Among authors: wohr g. Chromosome Res. 1998 Sep;6(6):429-35. doi: 10.1023/a:1009287223826. Chromosome Res. 1998. PMID: 9865780

8

Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22.

Eisenbarth I, König-Greger D, Wöhr G, Kehrer-Sawatzki H, Assum G. Eisenbarth I, et al. Among authors: wohr g. Chromosome Res. 1999;7(1):65-9. doi: 10.1023/a:1009279412797. Chromosome Res. 1999. PMID: 10219734

9

Evolution of the chAB4 multisequence family in primates.

Assum G, Gartmann C, Schempp W, Wöhr G. Assum G, et al. Among authors: wohr g. Genomics. 1994 May 1;21(1):34-41. doi: 10.1006/geno.1994.1221. Genomics. 1994. PMID: 8088813

10

A new multisequence family in human.

Assum G, Fink T, Klett C, Lengl B, Schanbacher M, Uhl S, Wöhr G. Assum G, et al. Among authors: wohr g. Genomics. 1991 Oct;11(2):397-409. doi: 10.1016/0888-7543(91)90148-8. Genomics. 1991. PMID: 1769654

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