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Results: 1-10 |
Results: 10
Molecular subtypes of anaplastic oligodendroglioma: Implications for patient management at diagnosis
Authors: Ino, Y Betensky, RA Zlatescu, MC Sasaki, H Macdonald, DR Stemmer-Rachamimov, AO Ramsay, DA Cairncross, JG Louis, DN
Citation: Y. Ino et al., Molecular subtypes of anaplastic oligodendroglioma: Implications for patient management at diagnosis, CLIN CANC R, 7(4), 2001, pp. 839-845
Pattern of self-organization in tumour systems: complex growth dynamics ina novel brain tumour spheroid model
Authors: Deisboeck, TS Berens, ME Kansal, AR Torquato, S Stemmer-Rachamimov, AO Chiocca, EA
Citation: Ts. Deisboeck et al., Pattern of self-organization in tumour systems: complex growth dynamics ina novel brain tumour spheroid model, CELL PROLIF, 34(2), 2001, pp. 115-134
NHE-RF, a merlin-interacting protein, is primarily expressed in luminal epithelia, proliferative endometrium, and estrogen receptor-positive breast carcinomas
Authors: Stemmer-Rachamimov, AO Wiederhold, T Nielsen, GP James, M Pinney-Michalowski, D Roy, JE Cohen, WA Ramesh, V Louis, DN
Citation: Ao. Stemmer-rachamimov et al., NHE-RF, a merlin-interacting protein, is primarily expressed in luminal epithelia, proliferative endometrium, and estrogen receptor-positive breast carcinomas, AM J PATH, 158(1), 2001, pp. 57-62
Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomassuggests different genetic mechanisms for pathogenesis of TSC lesions
Authors: Niida, Y Stemmer-Rachamimov, AO Logrip, M Tapon, D Perez, R Kwiatkowski, DJ Sims, K MacCollin, M Louis, DN Ramesh, V
Citation: Y. Niida et al., Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomassuggests different genetic mechanisms for pathogenesis of TSC lesions, AM J HU GEN, 69(3), 2001, pp. 493-503
Developmental expression of the tuberous sclerosis proteins tuberin and hamartin
Authors: Murthy, V Stemmer-Rachamimov, AO Haddad, LA Roy, JE Cutone, AN Beauchamp, RL Smith, N Louis, DN Ramesh, V
Citation: V. Murthy et al., Developmental expression of the tuberous sclerosis proteins tuberin and hamartin, ACT NEUROP, 101(3), 2001, pp. 202-210
Long survival and therapeutic responses in patients with histologically disparate high-grade gliomas demonstrating chromosome 1p loss
Authors: Ino, Y Zlatescu, MC Sasaki, H MacDonald, DR Stemmer-Rachamimov, AO Jhung, S Ramsay, DA von Deimling, A Louis, DN Cairncross, JG
Citation: Y. Ino et al., Long survival and therapeutic responses in patients with histologically disparate high-grade gliomas demonstrating chromosome 1p loss, J NEUROSURG, 92(6), 2000, pp. 983-990
Immunohistochemical survey of p16(INK4A) expression in normal human adult and infant tissues
Authors: Nielsen, GP Stemmer-Rachamimov, AO Shaw, J Roy, JE Koh, J Louis, DN
Citation: Gp. Nielsen et al., Immunohistochemical survey of p16(INK4A) expression in normal human adult and infant tissues, LAB INV, 79(9), 1999, pp. 1137-1143
The hPMS2 exon 5 mutation and malignant glioma
Authors: Taylor, MD Perry, J Zlatescu, MC Stemmer-Rachamimov, AO Ang, LC Ino, Y Schwartz, M Becker, LE Louis, DN Cairncross, JG
Citation: Md. Taylor et al., The hPMS2 exon 5 mutation and malignant glioma, J NEUROSURG, 90(5), 1999, pp. 946-950
Malignant transformation of neurofibromas in neurofibromatosis 1 is associated with CDKN2A/p16 inactivation
Authors: Nielsen, GP Stemmer-Rachamimov, AO Ino, Y Moller, MB Rosenberg, AE Louis, DN
Citation: Gp. Nielsen et al., Malignant transformation of neurofibromas in neurofibromatosis 1 is associated with CDKN2A/p16 inactivation, AM J PATH, 155(6), 1999, pp. 1879-1884
Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2
Authors: Stemmer-Rachamimov, AO Ino, Y Lim, ZY Jacoby, LB MacCollin, M Gusella, JF Ramesh, V Louis, DN
Citation: Ao. Stemmer-rachamimov et al., Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2, J NE EXP NE, 57(12), 1998, pp. 1164-1167
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