Murken J - Search Results

1

UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2.

Brandau O, Nyakatura G, Jedele KB, Platzer M, Achatz H, Ross M, Murken J, Rosenthal A, Meindl A. Brandau O, et al. Among authors: murken j. Eur J Hum Genet. 1998 Sep-Oct;6(5):459-66. doi: 10.1038/sj.ejhg.5200207. Eur J Hum Genet. 1998. PMID: 9801870

2

Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.

Holinski-Feder E, Chahrockh-Zadeh S, Rittinger O, Jedele KB, Gasteiger M, Lenski C, Murken J, Golla A. Holinski-Feder E, et al. Among authors: murken j. Am J Med Genet. 1999 Sep 10;86(2):102-6. doi: 10.1002/(sici)1096-8628(19990910)86:2<102::aid-ajmg2>3.0.co;2-c. Am J Med Genet. 1999. PMID: 10449641

3

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).

Schuffenhauer S, Lichtner P, Peykar-Derakhshandeh P, Murken J, Haas OA, Back E, Wolff G, Zabel B, Barisic I, Rauch A, Borochowitz Z, Dallapiccola B, Ross M, Meitinger T. Schuffenhauer S, et al. Among authors: murken j. Eur J Hum Genet. 1998 May-Jun;6(3):213-25. doi: 10.1038/sj.ejhg.5200183. Eur J Hum Genet. 1998. PMID: 9781025

4

Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure.

Meitinger T, Meindl A, Bork P, Rost B, Sander C, Haasemann M, Murken J. Meitinger T, et al. Among authors: murken j. Nat Genet. 1993 Dec;5(4):376-80. doi: 10.1038/ng1293-376. Nat Genet. 1993. PMID: 8298646

5

Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissues.

Jedele KB, Wahl D, Chahrokh-Zadeh S, Wirtz A, Murken J, Holinski-Feder E. Jedele KB, et al. Among authors: murken j. Clin Genet. 1998 Aug;54(2):148-51. doi: 10.1111/j.1399-0004.1998.tb03718.x. Clin Genet. 1998. PMID: 9761394

6

A PCR based X-chromosome inactivation assay for carrier detection in X-linked immunodeficiencies using differential methylation of the androgen receptor gene.

Schmucker B, Meindl A, Achatz H, Mittermüller J, Krüger G, Hergersberg M, Spiegel R, Schinzel A, Belohradsky BH, Murken J, et al. Schmucker B, et al. Among authors: murken j. Immunodeficiency. 1995;5(3):187-92. Immunodeficiency. 1995. PMID: 7749438

7

MRX42: two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation.

Golla A, Rost I, Jedele KB, Albert A, Murken J, Holinski-Feder E. Golla A, et al. Among authors: murken j. Am J Med Genet. 2002 Jan 1;107(1):18-25. doi: 10.1002/ajmg.10027. Am J Med Genet. 2002. PMID: 11807862

8

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene.

Coffey AJ, Brooksbank RA, Brandau O, Oohashi T, Howell GR, Bye JM, Cahn AP, Durham J, Heath P, Wray P, Pavitt R, Wilkinson J, Leversha M, Huckle E, Shaw-Smith CJ, Dunham A, Rhodes S, Schuster V, Porta G, Yin L, Serafini P, Sylla B, Zollo M, Franco B, Bolino A, Seri M, Lanyi A, Davis JR, Webster D, Harris A, Lenoir G, de St Basile G, Jones A, Behloradsky BH, Achatz H, Murken J, Fassler R, Sumegi J, Romeo G, Vaudin M, Ross MT, Meindl A, Bentley DR. Coffey AJ, et al. Among authors: murken j. Nat Genet. 1998 Oct;20(2):129-35. doi: 10.1038/2424. Nat Genet. 1998. PMID: 9771704

9

Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Meitinger T, Heye B, Petit C, Levilliers J, Golla A, Moraine C, Dalla Piccola B, Sippell WG, Murken J, Ballabio A. Meitinger T, et al. Among authors: murken j. Am J Hum Genet. 1990 Oct;47(4):664-9. Am J Hum Genet. 1990. PMID: 1977309 Free PMC article.

10

Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.

Jauch A, Daumer C, Lichter P, Murken J, Schroeder-Kurth T, Cremer T. Jauch A, et al. Among authors: murken j. Hum Genet. 1990 Jul;85(2):145-50. doi: 10.1007/BF00193186. Hum Genet. 1990. PMID: 2370043 Free article.

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