Ramesh V - Search Results

1

NHE-RF, a merlin-interacting protein, is primarily expressed in luminal epithelia, proliferative endometrium, and estrogen receptor-positive breast carcinomas.

Stemmer-Rachamimov AO, Wiederhold T, Nielsen GP, James M, Pinney-Michalowski D, Roy JE, Cohen WA, Ramesh V, Louis DN. Stemmer-Rachamimov AO, et al. Among authors: ramesh v. Am J Pathol. 2001 Jan;158(1):57-62. doi: 10.1016/S0002-9440(10)63944-2. Am J Pathol. 2001. PMID: 11141479 Free PMC article.

2

Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.

Louis DN, Ramesh V, Gusella JF. Louis DN, et al. Among authors: ramesh v. Brain Pathol. 1995 Apr;5(2):163-72. doi: 10.1111/j.1750-3639.1995.tb00590.x. Brain Pathol. 1995. PMID: 7670657 Review.

3

Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.

Wellenreuther R, Kraus JA, Lenartz D, Menon AG, Schramm J, Louis DN, Ramesh V, Gusella JF, Wiestler OD, von Deimling A. Wellenreuther R, et al. Among authors: ramesh v. Am J Pathol. 1995 Apr;146(4):827-32. Am J Pathol. 1995. PMID: 7717450 Free PMC article.

4

Evidence for subarachnoid spread in the development of multiple meningiomas.

von Deimling A, Kraus JA, Stangl AP, Wellenreuther R, Lenartz D, Schramm J, Louis DN, Ramesh V, Gusella JF, Wiestler OD. von Deimling A, et al. Among authors: ramesh v. Brain Pathol. 1995 Jan;5(1):11-4. doi: 10.1111/j.1750-3639.1995.tb00571.x. Brain Pathol. 1995. PMID: 7767486

5

MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p.

Ueki K, Rubio MP, Ramesh V, Correa KM, Rutter JL, von Deimling A, Buckler AJ, Gusella JF, Louis DN. Ueki K, et al. Among authors: ramesh v. Hum Mol Genet. 1994 Oct;3(10):1841-5. doi: 10.1093/hmg/3.10.1841. Hum Mol Genet. 1994. PMID: 7849711

6

Mutational analysis of patients with neurofibromatosis 2.

MacCollin M, Ramesh V, Jacoby LB, Louis DN, Rubio MP, Pulaski K, Trofatter JA, Short MP, Bove C, Eldridge R, et al. MacCollin M, et al. Among authors: ramesh v. Am J Hum Genet. 1994 Aug;55(2):314-20. Am J Hum Genet. 1994. PMID: 7913580 Free PMC article.

7

Exon scanning for mutation of the NF2 gene in schwannomas.

Jacoby LB, MacCollin M, Louis DN, Mohney T, Rubio MP, Pulaski K, Trofatter JA, Kley N, Seizinger B, Ramesh V, et al. Jacoby LB, et al. Among authors: ramesh v. Hum Mol Genet. 1994 Mar;3(3):413-9. doi: 10.1093/hmg/3.3.413. Hum Mol Genet. 1994. PMID: 8012353

8

Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas.

Rubio MP, Correa KM, Ramesh V, MacCollin MM, Jacoby LB, von Deimling A, Gusella JF, Louis DN. Rubio MP, et al. Among authors: ramesh v. Cancer Res. 1994 Jan 1;54(1):45-7. Cancer Res. 1994. PMID: 8261460

9

The merlin tumor suppressor localizes preferentially in membrane ruffles.

Gonzalez-Agosti C, Xu L, Pinney D, Beauchamp R, Hobbs W, Gusella J, Ramesh V. Gonzalez-Agosti C, et al. Among authors: ramesh v. Oncogene. 1996 Sep 19;13(6):1239-47. Oncogene. 1996. PMID: 8808698

10

Expression of NF2-encoded merlin and related ERM family proteins in the human central nervous system.

Stemmer-Rachamimov AO, Gonzalez-Agosti C, Xu L, Burwick JA, Beauchamp R, Pinney D, Louis DN, Ramesh V. Stemmer-Rachamimov AO, et al. Among authors: ramesh v. J Neuropathol Exp Neurol. 1997 Jun;56(6):735-42. J Neuropathol Exp Neurol. 1997. PMID: 9184664

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