Hahnen E - Search Results

1

Incorporating Alternative Polygenic Risk Scores into the BOADICEA Breast Cancer Risk Prediction Model.

Mavaddat N, Ficorella L, Carver T, Lee A, Cunningham AP, Lush M, Dennis J, Tischkowitz M, Downes K, Hu D, Hahnen E, Schmutzler RK, Stockley TL, Downs GS, Zhang T, Chiarelli AM, Bojesen SE, Liu C, Chung WK, Pardo M, Feliubadaló L, Balmaña J, Simard J, Antoniou AC, Easton DF. Mavaddat N, et al. Among authors: hahnen e. Cancer Epidemiol Biomarkers Prev. 2023 Mar 6;32(3):422-427. doi: 10.1158/1055-9965.EPI-22-0756. Cancer Epidemiol Biomarkers Prev. 2023. PMID: 36649146 Free PMC article.

2

PPAR Gamma Activators: Off-Target Against Glioma Cell Migration and Brain Invasion.

Seufert S, Coras R, Tränkle C, Zlotos DP, Blümcke I, Tatenhorst L, Heneka MT, Hahnen E. Seufert S, et al. Among authors: hahnen e. PPAR Res. 2008;2008:513943. doi: 10.1155/2008/513943. PPAR Res. 2008. PMID: 18815619 Free PMC article.

3

A novel secreted ribonuclease from Bacillus intermedius: gene structure and regulatory control.

Hahnen E, Znamenskaya L, Koczan D, Leshchinskaya I, Hobom G. Hahnen E, et al. Mol Gen Genet. 2000 May;263(4):571-80. doi: 10.1007/s004380051203. Mol Gen Genet. 2000. PMID: 10852477 Free article.

4

Common mutations of beta-catenin in adamantinomatous craniopharyngiomas but not in other tumours originating from the sellar region.

Buslei R, Nolde M, Hofmann B, Meissner S, Eyupoglu IY, Siebzehnrübl F, Hahnen E, Kreutzer J, Fahlbusch R. Buslei R, et al. Among authors: hahnen e. Acta Neuropathol. 2005 Jun;109(6):589-97. doi: 10.1007/s00401-005-1004-x. Epub 2005 May 13. Acta Neuropathol. 2005. PMID: 15891929

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. Am J Hum Genet. 1996 Nov;59(5):1057-65. Am J Hum Genet. 1996. PMID: 8900234 Free PMC article.

6

Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases.

Wirth B, Rudnik-Schöneborn S, Hahnen E, Röhrig D, Zerres K. Wirth B, et al. Among authors: hahnen e. Prenat Diagn. 1995 May;15(5):407-17. doi: 10.1002/pd.1970150503. Prenat Diagn. 1995. PMID: 7644431

7

De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling.

Wirth B, Schmidt T, Hahnen E, Rudnik-Schöneborn S, Krawczak M, Müller-Myhsok B, Schönling J, Zerres K. Wirth B, et al. Among authors: hahnen e. Am J Hum Genet. 1997 Nov;61(5):1102-11. doi: 10.1086/301608. Am J Hum Genet. 1997. PMID: 9345102 Free PMC article.

8

In vitro and ex vivo evaluation of second-generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy.

Hahnen E, Eyüpoglu IY, Brichta L, Haastert K, Tränkle C, Siebzehnrübl FA, Riessland M, Hölker I, Claus P, Romstöck J, Buslei R, Wirth B, Blümcke I. Hahnen E, et al. J Neurochem. 2006 Jul;98(1):193-202. doi: 10.1111/j.1471-4159.2006.03868.x. J Neurochem. 2006. PMID: 16805808 Free article.

9

Frequent DNA variant in exon 2a of the survival motor neuron gene (SMN): a further possibility for distinguishing the two copies of the gene.

Hahnen ET, Wirth B. Hahnen ET, et al. Hum Genet. 1996 Jul;98(1):122-3. doi: 10.1007/s004390050172. Hum Genet. 1996. PMID: 8682499

10

Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generations.

Rudnik-Schöneborn S, Zerres K, Hahnen E, Meng G, Voit T, Hanefeld F, Wirth B. Rudnik-Schöneborn S, et al. Among authors: hahnen e. Am J Hum Genet. 1996 Nov;59(5):1163-5. Am J Hum Genet. 1996. PMID: 8900246 Free PMC article. No abstract available.

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