Horsthemke B - Search Results

1

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.

Martin M, Maßhöfer L, Temming P, Rahmann S, Metz C, Bornfeld N, van de Nes J, Klein-Hitpass L, Hinnebusch AG, Horsthemke B, Lohmann DR, Zeschnigk M. Martin M, et al. Among authors: horsthemke b. Nat Genet. 2013 Aug;45(8):933-6. doi: 10.1038/ng.2674. Epub 2013 Jun 23. Nat Genet. 2013. PMID: 23793026 Free PMC article.

2

Chromosomal aberrations defining uveal melanoma of poor prognosis.

Prescher G, Bornfeld N, Horsthemke B, Becher R. Prescher G, et al. Among authors: horsthemke b. Lancet. 1992 Mar 14;339(8794):691-2. Lancet. 1992. PMID: 1347396 No abstract available.

3

Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanoma.

Horsthemke B, Prescher G, Bornfeld N, Becher R. Horsthemke B, et al. Genes Chromosomes Cancer. 1992 Apr;4(3):217-21. doi: 10.1002/gcc.2870040305. Genes Chromosomes Cancer. 1992. PMID: 1382562

4

Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis.

Lohmann D, Horsthemke B, Gillessen-Kaesbach G, Stefani FH, Höfler H. Lohmann D, et al. Among authors: horsthemke b. Hum Genet. 1992 Apr;89(1):49-53. doi: 10.1007/BF00207041. Hum Genet. 1992. PMID: 1577465

5

Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma.

Szijan I, Lohmann DR, Parma DL, Brandt B, Horsthemke B. Szijan I, et al. Among authors: horsthemke b. J Med Genet. 1995 Jun;32(6):475-9. doi: 10.1136/jmg.32.6.475. J Med Genet. 1995. PMID: 7666401 Free PMC article.

6

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B. Buiting K, et al. Among authors: horsthemke b. Nat Genet. 1995 Apr;9(4):395-400. doi: 10.1038/ng0495-395. Nat Genet. 1995. PMID: 7795645

7

Spectrum of small length germline mutations in the RB1 gene.

Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: horsthemke b. Hum Mol Genet. 1994 Dec;3(12):2187-93. doi: 10.1093/hmg/3.12.2187. Hum Mol Genet. 1994. PMID: 7881418

8

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.

Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Among authors: horsthemke b. Hum Genet. 1994 Oct;94(4):349-54. doi: 10.1007/BF00201591. Hum Genet. 1994. PMID: 7927327

9

Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma.

Greger V, Debus N, Lohmann D, Höpping W, Passarge E, Horsthemke B. Greger V, et al. Among authors: horsthemke b. Hum Genet. 1994 Nov;94(5):491-6. doi: 10.1007/BF00211013. Hum Genet. 1994. PMID: 7959682

10

Chromosomal gains and losses in uveal melanomas detected by comparative genomic hybridization.

Speicher MR, Prescher G, du Manoir S, Jauch A, Horsthemke B, Bornfeld N, Becher R, Cremer T. Speicher MR, et al. Among authors: horsthemke b. Cancer Res. 1994 Jul 15;54(14):3817-23. Cancer Res. 1994. PMID: 8033101

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