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Results: 1-25/30
Authors:
Weng, LP
Gimm, O
Kum, JB
Smith, WM
Zhou, XP
Wynford-Thomas, D
Leone, G
Eng, C
Citation: Lp. Weng et al., Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death, HUM MOL GEN, 10(3), 2001, pp. 251-258
Authors:
Gimm, O
Dziema, H
Brown, J
Cuong, HV
Hinze, R
Dralle, H
Mulligan, LM
Eng, C
Citation: O. Gimm et al., Over-representation of a germline variant in the gene encoding RET co-receptor GFR alpha-1 but not GFR alpha-2 or GFR alpha-3 in cases with sporadic medullary thyroid carcinoma, ONCOGENE, 20(17), 2001, pp. 2161-2170
Authors:
Vanhorne, JB
Gimm, O
Myers, SM
Kaushik, A
von Deimling, A
Eng, C
Mulligan, LM
Citation: Jb. Vanhorne et al., Cloning and characterization of the human GFRA2 locus and investigation ofthe gene in Hirschsprung disease, HUM GENET, 108(5), 2001, pp. 409-415
Authors:
Gimm, O
Citation: O. Gimm, Thyroid cancer, CANCER LETT, 163(2), 2001, pp. 143-156
Authors:
Gimm, O
Citation: O. Gimm, Multiple endocrine neoplasia type 2: Clinical aspects, FRONT HORM, 28, 2001, pp. 103-130
Authors:
Hinze, R
Gimm, O
Brauckhoff, M
Schneyer, U
Dralle, H
Holzhausen, HJ
Citation: R. Hinze et al., Physiological and neoplastic C-cell hyperplasia of the thyroid - morphologically and biologically distinct entities?, PATHOLOGE, 22(4), 2001, pp. 259-265
Authors:
Gimm, O
Sutter, T
Dralle, H
Citation: O. Gimm et al., Diagnosis and therapy of sporadic and familial medullary thyroid carcinoma, J CANC RES, 127(3), 2001, pp. 156-165
Authors:
Gimm, O
Chi, HB
Dahia, PLM
Perren, A
Hinze, R
Komminoth, P
Dralle, H
Reynolds, PR
Eng, C
Citation: O. Gimm et al., Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas, J CLIN END, 86(4), 2001, pp. 1801-1805
Authors:
Machens, A
Gimm, O
Hinze, R
Hoppner, W
Boehm, BO
Dralle, H
Citation: A. Machens et al., Genotype-phenotype correlations in hereditary medullary thyroid carcinoma:Oncological features and biochemical properties, J CLIN END, 86(3), 2001, pp. 1104-1109
Authors:
Gimm, O
Dziema, H
Brown, J
De la Puente, A
Hoang-Vu, C
Dralle, H
Plass, C
Eng, C
Citation: O. Gimm et al., Mutation analysis of NTRK2 and NTRK3, encoding 2 tyrosine kinase receptors, in sporadic human medullary thyroid carcinoma reveals novel sequence variants, INT J CANC, 92(1), 2001, pp. 70-74
Authors:
Gimm, O
Dralle, H
Citation: O. Gimm et H. Dralle, The current surgical approach to non-medullary thyroid cancer, THYROID CANCER, 2001, pp. 81-89
Authors:
Gimm, O
Dralle, H
Citation: O. Gimm et H. Dralle, Therapy for medullary thyroid cancer, THYROID CANCER, 2001, pp. 275-284
Authors:
Zhou, XP
Marsh, DJ
Hampel, H
Mulliken, JB
Gimm, O
Eng, C
Citation: Xp. Zhou et al., Germline and germline mosaic PTEN mutations associated with a Proteus-likesyndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis, HUM MOL GEN, 9(5), 2000, pp. 765-768
Authors:
Gimm, O
Attie-Bitach, T
Lees, JA
Vekemans, M
Eng, C
Citation: O. Gimm et al., Expression of the PTEN tumour suppressor protein during human development, HUM MOL GEN, 9(11), 2000, pp. 1633-1639
Authors:
Hinze, R
Gimm, O
Taubert, H
Bauer, G
Dralle, H
Holzhausen, HJ
Rath, FW
Citation: R. Hinze et al., Regulation of proliferation and apoptosis in sporadic and hereditary medullary thyroid carcinomas and their putative precursor lesions, VIRCHOWS AR, 437(3), 2000, pp. 256-263
Authors:
Dahia, PM
Gimm, O
Chi, HB
Marsh, DJ
Reynolds, PR
Eng, C
Citation: Pm. Dahia et al., Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations, J MED GENET, 37(9), 2000, pp. 715-717
Authors:
Borrego, S
Ruiz, A
Saez, ME
Gimm, O
Gao, X
Lopez-Alonso, M
Hernandez, A
Wright, FA
Antinolo, G
Eng, C
Citation: S. Borrego et al., RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease, J MED GENET, 37(8), 2000, pp. 572-578
Authors:
Zhou, XP
Smith, WM
Gimm, O
Mueller, E
Gao, X
Sarraf, P
Prior, TW
Plass, C
von Deimling, A
Black, PM
Yates, AJ
Eng, C
Citation: Xp. Zhou et al., Over-representation of PPAR gamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population, J MED GENET, 37(6), 2000, pp. 410-414
Authors:
Gimm, O
Armanios, M
Dziema, H
Neumann, HPH
Eng, C
Citation: O. Gimm et al., Somatic and occult germ-line mutations in SDHD, a mitochondrial complex IIgene, in nonfamilial pheochromocytoma, CANCER RES, 60(24), 2000, pp. 6822-6825
Authors:
Machens, A
Gimm, O
Ukkat, J
Hinze, R
Schneyer, U
Dralle, H
Citation: A. Machens et al., Improved prediction of calcitonin normalization in medullary thyroid carcinoma patients by quantitative lymph node analysis, CANCER, 88(8), 2000, pp. 1909-1915
Authors:
Zhou, XP
Gimm, O
Hampel, H
Niemann, T
Walker, MJ
Eng, C
Citation: Xp. Zhou et al., Epigenetic PTEN silencing in malignant melanomas without PTEN mutation, AM J PATH, 157(4), 2000, pp. 1123-1128
Authors:
Gimm, O
Perren, A
Weng, LP
Marsh, DJ
Yeh, JJ
Ziebold, U
Gil, E
Hinze, R
Delbridge, L
Lees, JA
Mutter, GL
Robinson, BG
Komminoth, P
Dralle, H
Eng, C
Citation: O. Gimm et al., Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors, AM J PATH, 156(5), 2000, pp. 1693-1700
Authors:
Machens, A
Gimm, O
Ukkat, J
Sutter, T
Dralle, H
Citation: A. Machens et al., Repeat mediastinal lymph-node dissection for palliation in advanced medullary thyroid carcinoma, LANG ARCH S, 384(3), 1999, pp. 271-276
Authors:
Gimm, O
Dralle, H
Citation: O. Gimm et H. Dralle, C-cell cancer - prevention and treatment, LANG ARCH S, 384(1), 1999, pp. 16-23
Authors:
Gimm, O
Neuberg, DS
Marsh, DJ
Dahia, PLM
Cuong, HV
Raue, F
Hinze, R
Dralle, H
Eng, C
Citation: O. Gimm et al., Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation, ONCOGENE, 18(6), 1999, pp. 1369-1373