Wolter M - Search Results

1

Rapid and sensitive assessment of the IDH1 and IDH2 mutation status in cerebral gliomas based on DNA pyrosequencing.

Felsberg J, Wolter M, Seul H, Friedensdorf B, Göppert M, Sabel MC, Reifenberger G. Felsberg J, et al. Among authors: wolter m. Acta Neuropathol. 2010 Apr;119(4):501-7. doi: 10.1007/s00401-010-0647-4. Epub 2010 Feb 4. Acta Neuropathol. 2010. PMID: 20131059

2

Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.

Wolter M, Reifenberger J, Sommer C, Ruzicka T, Reifenberger G. Wolter M, et al. Cancer Res. 1997 Jul 1;57(13):2581-5. Cancer Res. 1997. PMID: 9205058

3

Mutation of the PTEN (MMAC1) tumor suppressor gene in a subset of glioblastomas but not in meningiomas with loss of chromosome arm 10q.

Boström J, Cobbers JM, Wolter M, Tabatabai G, Weber RG, Lichter P, Collins VP, Reifenberger G. Boström J, et al. Among authors: wolter m. Cancer Res. 1998 Jan 1;58(1):29-33. Cancer Res. 1998. PMID: 9426052

4

Frequent inactivation of CDKN2A and rare mutation of TP53 in PCNSL.

Cobbers JM, Wolter M, Reifenberger J, Ring GU, Jessen F, An HX, Niederacher D, Schmidt EE, Ichimura K, Floeth F, Kirsch L, Borchard F, Louis DN, Collins VP, Reifenberger G. Cobbers JM, et al. Among authors: wolter m. Brain Pathol. 1998 Apr;8(2):263-76. doi: 10.1111/j.1750-3639.1998.tb00152.x. Brain Pathol. 1998. PMID: 9546285 Free PMC article.

5

Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.

Reifenberger J, Wolter M, Weber RG, Megahed M, Ruzicka T, Lichter P, Reifenberger G. Reifenberger J, et al. Among authors: wolter m. Cancer Res. 1998 May 1;58(9):1798-803. Cancer Res. 1998. PMID: 9581815

6

Expression of Bcl-2 and amplification of c-myc are frequent in basaloid squamous cell carcinomas of the esophagus.

Sarbia M, Loberg C, Wolter M, Arjumand J, Heep H, Reifenberger G, Gabbert HE. Sarbia M, et al. Among authors: wolter m. Am J Pathol. 1999 Oct;155(4):1027-32. doi: 10.1016/S0002-9440(10)65203-0. Am J Pathol. 1999. PMID: 10514383 Free PMC article.

7

Identification of two distinct deleted regions on the short arm of chromosome 1 and rare mutation of the CDKN2C gene from 1p32 in oligodendroglial tumors.

Husemann K, Wolter M, Büschges R, Boström J, Sabel M, Reifenberger G. Husemann K, et al. Among authors: wolter m. J Neuropathol Exp Neurol. 1999 Oct;58(10):1041-50. doi: 10.1097/00005072-199910000-00002. J Neuropathol Exp Neurol. 1999. PMID: 10515227

8

Amplification and overexpression of the MDM4 (MDMX) gene from 1q32 in a subset of malignant gliomas without TP53 mutation or MDM2 amplification.

Riemenschneider MJ, Büschges R, Wolter M, Reifenberger J, Boström J, Kraus JA, Schlegel U, Reifenberger G. Riemenschneider MJ, et al. Among authors: wolter m. Cancer Res. 1999 Dec 15;59(24):6091-6. Cancer Res. 1999. PMID: 10626796

9

Allelic losses on chromosome arm 10q and mutation of the PTEN (MMAC1) tumour suppressor gene in primary and metastatic malignant melanomas.

Reifenberger J, Wolter M, Boström J, Büschges R, Schulte KW, Megahed M, Ruzicka T, Reifenberger G. Reifenberger J, et al. Among authors: wolter m. Virchows Arch. 2000 May;436(5):487-93. doi: 10.1007/s004280050477. Virchows Arch. 2000. PMID: 10881743

10

Molecular genetic alterations in glioblastomas with oligodendroglial component.

Kraus JA, Lamszus K, Glesmann N, Beck M, Wolter M, Sabel M, Krex D, Klockgether T, Reifenberger G, Schlegel U. Kraus JA, et al. Among authors: wolter m. Acta Neuropathol. 2001 Apr;101(4):311-20. doi: 10.1007/s004010000258. Acta Neuropathol. 2001. PMID: 11355302

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