Nothwang HG - Search Results

1

Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13.

Hildebrandt F, Cybulla M, Strahm B, Nothwang HG, Singh-Sawhney I, Berz K, Nicklin M, Reiner O, Brandis M. Hildebrandt F, et al. Among authors: nothwang hg. Cytogenet Cell Genet. 1996;73(3):235-9. doi: 10.1159/000134346. Cytogenet Cell Genet. 1996. PMID: 8697815

2

Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Hildebrandt F, Strahm B, Nothwang HG, Gretz N, Schnieders B, Singh-Sawhney I, Kutt R, Vollmer M, Brandis M. Hildebrandt F, et al. Among authors: nothwang hg. Kidney Int. 1997 Jan;51(1):261-9. doi: 10.1038/ki.1997.31. Kidney Int. 1997. PMID: 8995741 Free article.

3

Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13.

Nothwang HG, Strahm B, Denich D, Kübler M, Schwabe J, Gingrich JC, Jauch A, Cox A, Nicklin MJ, Kurnit DM, Hildebrandt F. Nothwang HG, et al. Genomics. 1997 May 1;41(3):370-8. doi: 10.1006/geno.1997.4654. Genomics. 1997. PMID: 9169134

4

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.

Hildebrandt F, Otto E, Rensing C, Nothwang HG, Vollmer M, Adolphs J, Hanusch H, Brandis M. Hildebrandt F, et al. Among authors: nothwang hg. Nat Genet. 1997 Oct;17(2):149-53. doi: 10.1038/ng1097-149. Nat Genet. 1997. PMID: 9326933

5

Construction of a gene map of the nephronophthisis type 1 (NPHP1) region on human chromosome 2q12-q13.

Nothwang HG, Stubanus M, Adolphs J, Hanusch H, Vossmerbäumer U, Denich D, Kübler M, Mincheva A, Lichter P, Hildebrandt F. Nothwang HG, et al. Genomics. 1998 Jan 15;47(2):276-85. doi: 10.1006/geno.1997.5102. Genomics. 1998. PMID: 9479500

6

Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Hildebrandt F, Nothwang HG, Vossmerbäumer U, Springer C, Strahm B, Hoppe B, Keuth B, Fuchshuber A, Querfeld U, Neuhaus TJ, Brandis M. Hildebrandt F, et al. Among authors: nothwang hg. Pediatr Nephrol. 1998 Jan;12(1):16-9. doi: 10.1007/s004670050394. Pediatr Nephrol. 1998. PMID: 9502560

7

Human adolescent nephronophthisis: gene locus synteny with polycystic kidney disease in pcy mice.

Omran H, Häffner K, Burth S, Fernandez C, Fargier B, Villaquiran A, Nothwang HG, Schnittger S, Lehrach H, Woo D, Brandis M, Sudbrak R, Hildebrandt F. Omran H, et al. Among authors: nothwang hg. J Am Soc Nephrol. 2001 Jan;12(1):107-113. doi: 10.1681/ASN.V121107. J Am Soc Nephrol. 2001. PMID: 11134256

8

Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996.

Spur NK, Bashir R, Bushby K, Cox A, Cox S, Hilde Brandt F, Hill N, Kao FT, Krols L, Marzella R, Miller N, Nothwang HG, Rocchi M, Sarfarazi M, Stratakis CA, Wallgren-Petterson C, Naylor S. Spur NK, et al. Among authors: nothwang hg. Cytogenet Cell Genet. 1996;73(4):255-73. doi: 10.1159/000134352. Cytogenet Cell Genet. 1996. PMID: 8751373 No abstract available.

9

Identification of a novel Ran binding protein 2 related gene (RANBP2L1) and detection of a gene cluster on human chromosome 2q11-q12.

Nothwang HG, Rensing C, Kübler M, Denich D, Brandl B, Stubanus M, Haaf T, Kurnit D, Hildebrandt F. Nothwang HG, et al. Genomics. 1998 Feb 1;47(3):383-92. doi: 10.1006/geno.1997.5119. Genomics. 1998. PMID: 9480752

10

Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes.

Vollmer M, Kremer M, Ruf R, Miot S, Nothwang HG, Wirth J, Otto E, Krapf R, Hildebrandt F. Vollmer M, et al. Among authors: nothwang hg. Genomics. 2000 Sep 1;68(2):127-35. doi: 10.1006/geno.2000.6292. Genomics. 2000. PMID: 10964510

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