Rosenthal A - Search Results

1

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Schwahn U, Lenzner S, Dong J, Feil S, Hinzmann B, van Duijnhoven G, Kirschner R, Hemberger M, Bergen AA, Rosenberg T, Pinckers AJ, Fundele R, Rosenthal A, Cremers FP, Ropers HH, Berger W. Schwahn U, et al. Among authors: rosenthal a. Nat Genet. 1998 Aug;19(4):327-32. doi: 10.1038/1214. Nat Genet. 1998. PMID: 9697692

2

Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP).

Roepman R, Bauer D, Rosenberg T, van Duijnhoven G, van de Vosse E, Platzer M, Rosenthal A, Ropers HH, Cremers FP, Berger W. Roepman R, et al. Among authors: rosenthal a. Hum Mol Genet. 1996 Jun;5(6):827-33. doi: 10.1093/hmg/5.6.827. Hum Mol Genet. 1996. PMID: 8776599 Free article.

3

Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.

Nothwang HG, Schröer A, van der Maarel S, Kübart S, Schneider S, Riesselmann L, Menzel C, Hinzmann B, Vogt D, Rosenthal A, Fryns J, Tommerup N, Haaf T, Ropers HH, Wirth J. Nothwang HG, et al. Among authors: rosenthal a. Cytogenet Cell Genet. 2000;90(1-2):126-33. doi: 10.1159/000015647. Cytogenet Cell Genet. 2000. PMID: 11060462

4

A genome-wide survey of RAS transformation targets.

Zuber J, Tchernitsa OI, Hinzmann B, Schmitz AC, Grips M, Hellriegel M, Sers C, Rosenthal A, Schäfer R. Zuber J, et al. Among authors: rosenthal a. Nat Genet. 2000 Feb;24(2):144-52. doi: 10.1038/72799. Nat Genet. 2000. PMID: 10655059

5

Genomic structure of a novel LIM domain gene (ZNF185) in Xq28 and comparisons with the orthologous murine transcript.

Heiss NS, Gloeckner G, Bächner D, Kioschis P, Klauck SM, Hinzmann B, Rosenthal A, Herman GE, Poustka A. Heiss NS, et al. Among authors: rosenthal a. Genomics. 1997 Aug 1;43(3):329-38. doi: 10.1006/geno.1997.4810. Genomics. 1997. PMID: 9268636

6

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Rao E, Weiss B, Fukami M, Rump A, Niesler B, Mertz A, Muroya K, Binder G, Kirsch S, Winkelmann M, Nordsiek G, Heinrich U, Breuning MH, Ranke MB, Rosenthal A, Ogata T, Rappold GA. Rao E, et al. Among authors: rosenthal a. Nat Genet. 1997 May;16(1):54-63. doi: 10.1038/ng0597-54. Nat Genet. 1997. PMID: 9140395

7

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.

Strom TM, Nyakatura G, Apfelstedt-Sylla E, Hellebrand H, Lorenz B, Weber BH, Wutz K, Gutwillinger N, Rüther K, Drescher B, Sauer C, Zrenner E, Meitinger T, Rosenthal A, Meindl A. Strom TM, et al. Among authors: rosenthal a. Nat Genet. 1998 Jul;19(3):260-3. doi: 10.1038/940. Nat Genet. 1998. PMID: 9662399

8

A novel repeat in the melanoma-associated chondroitin sulfate proteoglycan defines a new protein family.

Staub E, Hinzmann B, Rosenthal A. Staub E, et al. Among authors: rosenthal a. FEBS Lett. 2002 Sep 11;527(1-3):114-8. doi: 10.1016/s0014-5793(02)03195-2. FEBS Lett. 2002. PMID: 12220645 Free article.

9

A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer.

Staub E, Gröne J, Mennerich D, Röpcke S, Klamann I, Hinzmann B, Castanos-Velez E, Mann B, Pilarsky C, Brümmendorf T, Weber B, Buhr HJ, Rosenthal A. Staub E, et al. Among authors: rosenthal a. Mol Cancer. 2006 Sep 18;5:37. doi: 10.1186/1476-4598-5-37. Mol Cancer. 2006. PMID: 16982006 Free PMC article.

10

Exhaustive mining of EST libraries for genes differentially expressed in normal and tumour tissues.

Schmitt AO, Specht T, Beckmann G, Dahl E, Pilarsky CP, Hinzmann B, Rosenthal A. Schmitt AO, et al. Among authors: rosenthal a. Nucleic Acids Res. 1999 Nov 1;27(21):4251-60. doi: 10.1093/nar/27.21.4251. Nucleic Acids Res. 1999. PMID: 10518618 Free PMC article.

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