Müller U - Search Results

1

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).

Müller U, Haberhausen G, Wagner T, Fairweather ND, Chelly J, Monaco AP. Müller U, et al. Genomics. 1994 Sep 1;23(1):114-7. doi: 10.1006/geno.1994.1465. Genomics. 1994. PMID: 7829058

2

Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.

Haberhausen G, Schmitt I, Köhler A, Peters U, Rider S, Chelly J, Terwilliger JD, Monaco AP, Müller U. Haberhausen G, et al. Among authors: muller u. Am J Hum Genet. 1995 Sep;57(3):644-50. Am J Hum Genet. 1995. PMID: 7668293 Free PMC article.

3

AFX1 and p54nrb: fine mapping, genomic structure, and exclusion as candidate genes of X-linked dystonia parkinsonism.

Peters U, Haberhausen G, Kostrzewa M, Nolte D, Müller U. Peters U, et al. Among authors: muller u. Hum Genet. 1997 Oct;100(5-6):569-72. doi: 10.1007/s004390050553. Hum Genet. 1997. PMID: 9341872

4

Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3).

Németh AH, Nolte D, Dunne E, Niemann S, Kostrzewa M, Peters U, Fraser E, Bochukova E, Butler R, Brown J, Cox RD, Levy ER, Ropers HH, Monaco AP, Müller U. Németh AH, et al. Among authors: muller u. Genomics. 1999 Sep 15;60(3):320-9. doi: 10.1006/geno.1999.5929. Genomics. 1999. PMID: 10493831

5

A rapid and efficient method for the cloning of cosmid end-pieces.

Haberhausen G, Müller U. Haberhausen G, et al. Among authors: muller u. Nucleic Acids Res. 1995 Apr 25;23(8):1441-2. doi: 10.1093/nar/23.8.1441. Nucleic Acids Res. 1995. PMID: 7753638 Free PMC article.

6

Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12.

Fletcher FA, Huebner K, Shaffer LG, Fairweather ND, Monaco AP, Müller U, Druck T, Simoneaux DK, Chelly J, Belmont JW, et al. Fletcher FA, et al. Among authors: muller u. Genomics. 1995 Jan 1;25(1):334-5. doi: 10.1016/0888-7543(95)80156-g. Genomics. 1995. PMID: 7774950 No abstract available.

7

Fine mapping of the human SCIDX1 locus at Xq12-13.1.

Markiewicz S, DiSanto JP, Chelly J, Fairweather N, Le Marec B, Griscelli C, Graeber MB, Müller U, Fischer A, Monaco AP, et al. Markiewicz S, et al. Among authors: muller u. Hum Mol Genet. 1993 Jun;2(6):651-4. doi: 10.1093/hmg/2.6.651. Hum Mol Genet. 1993. PMID: 8353486

8

Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33.

Kostrzewa M, Köhler A, Eppelt K, Hellam L, Fairweather ND, Levy ER, Monaco AP, Müller U. Kostrzewa M, et al. Among authors: muller u. Eur J Hum Genet. 1996;4(4):199-204. doi: 10.1159/000472199. Eur J Hum Genet. 1996. PMID: 8875185

9

Novel genes mapping to the critical region of the 5q- syndrome.

Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS. Boultwood J, et al. Among authors: muller u. Genomics. 1997 Oct 1;45(1):88-96. doi: 10.1006/geno.1997.4899. Genomics. 1997. PMID: 9339364 Free article.

10

Integrated physical and transcript map of 5q31.3-qter.

Kostrzewa M, Krings BW, Dixon MJ, Eppelt K, Köhler A, Grady DL, Steinberger D, Fairweather ND, Moyzis RK, Monaco AP, Müller U. Kostrzewa M, et al. Among authors: muller u. Eur J Hum Genet. 1998 May-Jun;6(3):266-74. doi: 10.1038/sj.ejhg.5200188. Eur J Hum Genet. 1998. PMID: 9781031

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

2,050 results

Search Page