von Deimling A - Search Results

1

Somatic mitochondrial mutations in pilocytic astrocytoma.

Lueth M, Wronski L, Giese A, Kirschner-Schwabe R, Pietsch T, von Deimling A, Henze G, Kurtz A, Driever PH. Lueth M, et al. Among authors: von deimling a. Cancer Genet Cytogenet. 2009 Jul;192(1):30-5. doi: 10.1016/j.cancergencyto.2009.03.002. Cancer Genet Cytogenet. 2009. PMID: 19480934

2

p53 mutations are associated with 17p allelic loss in grade II and grade III astrocytoma.

von Deimling A, Eibl RH, Ohgaki H, Louis DN, von Ammon K, Petersen I, Kleihues P, Chung RY, Wiestler OD, Seizinger BR. von Deimling A, et al. Among authors: von ammon k. Cancer Res. 1992 May 15;52(10):2987-90. Cancer Res. 1992. PMID: 1349850

3

Loss of maternal alleles on chromosome arm 11p in hepatoblastoma.

Albrecht S, von Schweinitz D, Waha A, Kraus JA, von Deimling A, Pietsch T. Albrecht S, et al. Among authors: von deimling a, von schweinitz d. Cancer Res. 1994 Oct 1;54(19):5041-4. Cancer Res. 1994. PMID: 7923113

4

Loss of heterozygosity at locus F13B on chromosome 1q in human medulloblastoma.

Kraus JA, Koch A, Albrecht S, Von Deimling A, Wiestler OD, Pietsch T. Kraus JA, et al. Among authors: von deimling a. Int J Cancer. 1996 Jul 3;67(1):11-5. doi: 10.1002/(SICI)1097-0215(19960703)67:1<11::AID-IJC3>3.0.CO;2-2. Int J Cancer. 1996. PMID: 8690510

5

Expression and distribution of vascular endothelial growth factor protein in human brain tumors.

Pietsch T, Valter MM, Wolf HK, von Deimling A, Huang HJ, Cavenee WK, Wiestler OD. Pietsch T, et al. Among authors: von deimling a. Acta Neuropathol. 1997 Feb;93(2):109-17. doi: 10.1007/s004010050591. Acta Neuropathol. 1997. PMID: 9039457

6

Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched.

Pietsch T, Waha A, Koch A, Kraus J, Albrecht S, Tonn J, Sörensen N, Berthold F, Henk B, Schmandt N, Wolf HK, von Deimling A, Wainwright B, Chenevix-Trench G, Wiestler OD, Wicking C. Pietsch T, et al. Among authors: von deimling a. Cancer Res. 1997 Jun 1;57(11):2085-8. Cancer Res. 1997. PMID: 9187099

7

Molecular genetic analysis of ependymal tumors. NF2 mutations and chromosome 22q loss occur preferentially in intramedullary spinal ependymomas.

Ebert C, von Haken M, Meyer-Puttlitz B, Wiestler OD, Reifenberger G, Pietsch T, von Deimling A. Ebert C, et al. Among authors: von deimling a, von haken m. Am J Pathol. 1999 Aug;155(2):627-32. doi: 10.1016/S0002-9440(10)65158-9. Am J Pathol. 1999. PMID: 10433955 Free PMC article.

8

Low frequency of SV40, JC and BK polyomavirus sequences in human medulloblastomas, meningiomas and ependymomas.

Weggen S, Bayer TA, von Deimling A, Reifenberger G, von Schweinitz D, Wiestler OD, Pietsch T. Weggen S, et al. Among authors: von deimling a, von schweinitz d. Brain Pathol. 2000 Jan;10(1):85-92. doi: 10.1111/j.1750-3639.2000.tb00245.x. Brain Pathol. 2000. PMID: 10668898 Free PMC article.

9

INI1 mutations in meningiomas at a potential hotspot in exon 9.

Schmitz U, Mueller W, Weber M, Sévenet N, Delattre O, von Deimling A. Schmitz U, et al. Among authors: von deimling a. Br J Cancer. 2001 Jan;84(2):199-201. doi: 10.1054/bjoc.2000.1583. Br J Cancer. 2001. PMID: 11161377 Free PMC article.

10

Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.

Kraus JA, de Millas W, Sörensen N, Herbold C, Schichor C, Tonn JC, Wiestler OD, von Deimling A, Pietsch T. Kraus JA, et al. Among authors: von deimling a. Acta Neuropathol. 2001 Jul;102(1):69-74. doi: 10.1007/s004010000353. Acta Neuropathol. 2001. PMID: 11547953

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

839 results

Search Page

Filters