Herterich S - Search Results

1

Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.

Gross M, Hanenberg H, Lobitz S, Friedl R, Herterich S, Dietrich R, Gruhn B, Schindler D, Hoehn H. Gross M, et al. Among authors: herterich s. Cytogenet Genome Res. 2002;98(2-3):126-35. doi: 10.1159/000069805. Cytogenet Genome Res. 2002. PMID: 12697994

2

Disruption of the FA/BRCA pathway in bladder cancer.

Neveling K, Kalb R, Florl AR, Herterich S, Friedl R, Hoehn H, Hader C, Hartmann FH, Nanda I, Steinlein C, Schmid M, Tonnies H, Hurst CD, Knowles MA, Hanenberg H, Schulz WA, Schindler D. Neveling K, et al. Among authors: herterich s. Cytogenet Genome Res. 2007;118(2-4):166-76. doi: 10.1159/000108297. Cytogenet Genome Res. 2007. PMID: 18000367

3

Lack of sensitivity of primary Fanconi's anemia fibroblasts to UV and ionizing radiation.

Kalb R, Duerr M, Wagner M, Herterich S, Gross M, Digweed M, Joenje H, Hoehn H, Schindler D. Kalb R, et al. Among authors: herterich s. Radiat Res. 2004 Mar;161(3):318-25. doi: 10.1667/rr3138. Radiat Res. 2004. PMID: 14982482 Free article.

4

Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot study.

Bechtold A, Friedl R, Kalb R, Gottwald B, Neveling K, Gavvovidis I, Herterich S, Schindler D, Hoehn H. Bechtold A, et al. Among authors: herterich s. Fetal Diagn Ther. 2006;21(1):118-24. doi: 10.1159/000089061. Fetal Diagn Ther. 2006. PMID: 16354989

5

Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system.

Reuter T, Herterich S, Bernhard O, Hoehn H, Gross HJ. Reuter T, et al. Among authors: herterich s. Blood. 2000 Jan 15;95(2):719-20. Blood. 2000. PMID: 10627486 Free article.

6

Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport.

Reuter TY, Medhurst AL, Waisfisz Q, Zhi Y, Herterich S, Hoehn H, Gross HJ, Joenje H, Hoatlin ME, Mathew CG, Huber PA. Reuter TY, et al. Among authors: herterich s. Exp Cell Res. 2003 Oct 1;289(2):211-21. doi: 10.1016/s0014-4827(03)00261-1. Exp Cell Res. 2003. PMID: 14499622

7

Exclusion/confirmation of ataxia-telangiectasia via cell-cycle testing.

Heinrich T, Prowald C, Friedl R, Gottwald B, Kalb R, Neveling K, Herterich S, Hoehn H, Schindler D. Heinrich T, et al. Among authors: herterich s. Eur J Pediatr. 2006 Apr;165(4):250-7. doi: 10.1007/s00431-005-0037-4. Epub 2006 Jan 13. Eur J Pediatr. 2006. PMID: 16411093

8

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.

Wijker M, Morgan NV, Herterich S, van Berkel CG, Tipping AJ, Gross HJ, Gille JJ, Pals G, Savino M, Altay C, Mohan S, Dokal I, Cavenagh J, Marsh J, van Weel M, Ortega JJ, Schuler D, Samochatova E, Karwacki M, Bekassy AN, Abecasis M, Ebell W, Kwee ML, de Ravel T, CG Mathew, et al. Wijker M, et al. Among authors: herterich s. Eur J Hum Genet. 1999 Jan;7(1):52-9. doi: 10.1038/sj.ejhg.5200248. Eur J Hum Genet. 1999. PMID: 10094191

9

A novel patient-derived cell line of adrenocortical carcinoma shows a pathogenic role of germline MUTYH mutation and high tumour mutational burden.

Landwehr LS, Schreiner J, Appenzeller S, Kircher S, Herterich S, Sbiera S, Fassnacht M, Kroiss M, Weigand I. Landwehr LS, et al. Among authors: herterich s. Eur J Endocrinol. 2021 May 4;184(6):823-835. doi: 10.1530/EJE-20-1423. Eur J Endocrinol. 2021. PMID: 33830941

10

A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.

Reif A, Herterich S, Strobel A, Ehlis AC, Saur D, Jacob CP, Wienker T, Töpner T, Fritzen S, Walter U, Schmitt A, Fallgatter AJ, Lesch KP. Reif A, et al. Among authors: herterich s. Mol Psychiatry. 2006 Mar;11(3):286-300. doi: 10.1038/sj.mp.4001779. Mol Psychiatry. 2006. PMID: 16389274

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