Wirth B - Search Results

1

Comparative sequence analysis of the mouse and human Lgn1/SMA interval.

Endrizzi M, Huang S, Scharf JM, Kelter AR, Wirth B, Kunkel LM, Miller W, Dietrich WF. Endrizzi M, et al. Among authors: wirth b. Genomics. 1999 Sep 1;60(2):137-51. doi: 10.1006/geno.1999.5910. Genomics. 1999. PMID: 10486205

2

Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellites.

Wirth B, el-Agwany A, Baasner A, Burghes A, Koch A, Dadze A, Piechaczeck-Wappenschmidt B, Rudnik-Schöneborn S, Zerres K, Schönling J. Wirth B, et al. Eur J Hum Genet. 1995;3(1):56-60. doi: 10.1159/000472274. Eur J Hum Genet. 1995. PMID: 7767657

3

Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.

Wirth B, Pick E, Leutner A, Dadze A, Voosen B, Knapp M, Piechaczek-Wappenschmidt B, Rudnik-Schöneborn S, Schönling J, Cox S, et al. Wirth B, et al. Genomics. 1994 Mar 1;20(1):84-93. doi: 10.1006/geno.1994.1130. Genomics. 1994. PMID: 7912691

4

Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies.

Wirth B, Voosen B, Röhrig D, Knapp M, Piechaczek B, Rudnik-Schöneborn S, Zerres K. Wirth B, et al. Genomics. 1993 Jan;15(1):113-8. doi: 10.1006/geno.1993.1018. Genomics. 1993. PMID: 8432521

5

Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease.

Hahnen E, Schönling J, Rudnik-Schöneborn S, Zerres K, Wirth B. Hahnen E, et al. Among authors: wirth b. Am J Hum Genet. 1996 Nov;59(5):1057-65. Am J Hum Genet. 1996. PMID: 8900234 Free PMC article.

6

Missense mutations in exon 6 of the survival motor neuron gene in patients with spinal muscular atrophy (SMA).

Hahnen E, Schönling J, Rudnik-Schöneborn S, Raschke H, Zerres K, Wirth B. Hahnen E, et al. Among authors: wirth b. Hum Mol Genet. 1997 May;6(5):821-5. doi: 10.1093/hmg/6.5.821. Hum Mol Genet. 1997. PMID: 9158159

7

Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics.

Scharf JM, Endrizzi MG, Wetter A, Huang S, Thompson TG, Zerres K, Dietrich WF, Wirth B, Kunkel LM. Scharf JM, et al. Among authors: wirth b. Nat Genet. 1998 Sep;20(1):83-6. doi: 10.1038/1753. Nat Genet. 1998. PMID: 9731538

8

Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma.

von Deimling F, Scharf JM, Liehr T, Rothe M, Kelter AR, Albers P, Dietrich WF, Kunkel LM, Wernert N, Wirth B. von Deimling F, et al. Among authors: wirth b. Hum Genet. 1999 Jul-Aug;105(1-2):17-27. doi: 10.1007/s004399900067. Hum Genet. 1999. PMID: 10480350

9

The transcription factor-like nuclear regulator (TFNR) contains a novel 55-amino-acid motif repeated nine times and maps closely to SMN1.

Kelter AR, Herchenbach J, Wirth B. Kelter AR, et al. Among authors: wirth b. Genomics. 2000 Dec 15;70(3):315-26. doi: 10.1006/geno.2000.6396. Genomics. 2000. PMID: 11161782

10

Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markers.

Somlo S, Wirth B, Germino GG, Weinstat-Saslow D, Gillespie GA, Himmelbauer H, Steevens L, Coucke P, Willems P, Bachner L, et al. Somlo S, et al. Among authors: wirth b. Genomics. 1992 May;13(1):152-8. doi: 10.1016/0888-7543(92)90215-e. Genomics. 1992. PMID: 1349570

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