Stuhrmann M - Search Results

1

Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients.

Dörk T, Bendix R, Bremer M, Rades D, Klöpper K, Nicke M, Skawran B, Hector A, Yamini P, Steinmann D, Weise S, Stuhrmann M, Karstens JH. Dörk T, et al. Among authors: stuhrmann m. Cancer Res. 2001 Oct 15;61(20):7608-15. Cancer Res. 2001. PMID: 11606401

2

A frequent polymorphism of the gene mutated in ataxia telangiectasia.

Dörk T, Westermann S, Dittrich O, Twardowski M, Karstens JH, Schmidtke J, Stuhrmann M. Dörk T, et al. Among authors: stuhrmann m. Mol Cell Probes. 1997 Feb;11(1):71-3. doi: 10.1006/mcpr.1996.0079. Mol Cell Probes. 1997. PMID: 9076718

3

Polymorphisms of the human beta-defensin-1 gene.

Dörk T, Stuhrmann M. Dörk T, et al. Among authors: stuhrmann m. Mol Cell Probes. 1998 Jun;12(3):171-3. doi: 10.1006/mcpr.1998.0165. Mol Cell Probes. 1998. PMID: 9664579

4

Characterization of ATM gene mutations in 66 ataxia telangiectasia families.

Sandoval N, Platzer M, Rosenthal A, Dörk T, Bendix R, Skawran B, Stuhrmann M, Wegner RD, Sperling K, Banin S, Shiloh Y, Baumer A, Bernthaler U, Sennefelder H, Brohm M, Weber BH, Schindler D. Sandoval N, et al. Among authors: stuhrmann m. Hum Mol Genet. 1999 Jan;8(1):69-79. doi: 10.1093/hmg/8.1.69. Hum Mol Genet. 1999. PMID: 9887333

5

Frequency of BRCA1 mutation 5382insC in German breast cancer patients.

Backe J, Hofferbert S, Skawran B, Dörk T, Stuhrmann M, Karstens JH, Untch M, Meindl A, Burgemeister R, Chang-Claude J, Weber BH. Backe J, et al. Among authors: stuhrmann m. Gynecol Oncol. 1999 Mar;72(3):402-6. doi: 10.1006/gyno.1998.5270. Gynecol Oncol. 1999. PMID: 10053113

6

CFTR gene mutations and male infertility.

Stuhrmann M, Dörk T. Stuhrmann M, et al. Andrologia. 2000 Mar;32(2):71-83. doi: 10.1046/j.1439-0272.2000.00327.x. Andrologia. 2000. PMID: 10755189 Review.

7

A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis.

Will K, Dörk T, Stuhrmann M, Meitinger T, Bertele-Harms R, Tümmler B, Schmidtke J. Will K, et al. Among authors: stuhrmann m. J Clin Invest. 1994 Apr;93(4):1852-9. doi: 10.1172/JCI117172. J Clin Invest. 1994. PMID: 7512993 Free PMC article.

8

Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosis.

el-Harith EA, Dörk T, Stuhrmann M, Abu-Srair H, al-Shahri A, Keller KM, Lentze MJ, Schmidtke J. el-Harith EA, et al. Among authors: stuhrmann m. J Med Genet. 1997 Dec;34(12):996-9. doi: 10.1136/jmg.34.12.996. J Med Genet. 1997. PMID: 9429141 Free PMC article.

9

Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis.

Ockenga J, Stuhrmann M, Ballmann M, Teich N, Keim V, Dörk T, Manns MP. Ockenga J, et al. Among authors: stuhrmann m. Am J Gastroenterol. 2000 Aug;95(8):2061-7. doi: 10.1111/j.1572-0241.2000.02228.x. Am J Gastroenterol. 2000. PMID: 10950058

10

A termination mutation (2143delT) in the CFTR gene of German cystic fibrosis patients.

Dörk T, Kälin N, Stuhrmann M, Schmidtke J, Tümmler B. Dörk T, et al. Among authors: stuhrmann m. Hum Genet. 1992 Nov;90(3):279-84. doi: 10.1007/BF00220079. Hum Genet. 1992. PMID: 1283149

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

140 results

Search Page