Gimm O - Search Results

1

RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.

Borrego S, Ruiz A, Saez ME, Gimm O, Gao X, López-Alonso M, Hernández A, Wright FA, Antiñolo G, Eng C. Borrego S, et al. Among authors: gimm o. J Med Genet. 2000 Aug;37(8):572-8. doi: 10.1136/jmg.37.8.572. J Med Genet. 2000. PMID: 10922382 Free PMC article.

2

Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression.

Borrego S, Sáez ME, Ruiz A, Gimm O, López-Alonso M, Antiñolo G, Eng C. Borrego S, et al. Among authors: gimm o. J Med Genet. 1999 Oct;36(10):771-4. doi: 10.1136/jmg.36.10.771. J Med Genet. 1999. PMID: 10528857 Free PMC article.

3

Over-representation of PPARgamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population.

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. Zhou XP, et al. Among authors: gimm o. J Med Genet. 2000 Jun;37(6):410-4. doi: 10.1136/jmg.37.6.410. J Med Genet. 2000. PMID: 10851250 Free PMC article.

4

Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease.

Vanhorne JB, Gimm O, Myers SM, Kaushik A, von Deimling A, Eng C, Mulligan LM. Vanhorne JB, et al. Among authors: gimm o. Hum Genet. 2001 May;108(5):409-15. doi: 10.1007/s004390100506. Hum Genet. 2001. PMID: 11409869

5

Mutation analysis reveals novel sequence variants in NTRK1 in sporadic human medullary thyroid carcinoma.

Gimm O, Greco A, Hoang-Vu C, Dralle H, Pierotti MA, Eng C. Gimm O, et al. J Clin Endocrinol Metab. 1999 Aug;84(8):2784-7. doi: 10.1210/jcem.84.8.5901. J Clin Endocrinol Metab. 1999. PMID: 10443680

6

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.

Dahia PM, Gimm O, Chi H, Marsh DJ, Reynolds PR, Eng C. Dahia PM, et al. Among authors: gimm o. J Med Genet. 2000 Sep;37(9):715-7. doi: 10.1136/jmg.37.9.715. J Med Genet. 2000. PMID: 11182934 Free PMC article. No abstract available.

7

Over-representation of a germline variant in the gene encoding RET co-receptor GFRalpha-1 but not GFRalpha-2 or GFRalpha-3 in cases with sporadic medullary thyroid carcinoma.

Gimm O, Dziema H, Brown J, Hoang-Vu C, Hinze R, Dralle H, Mulligan LM, Eng C. Gimm O, et al. Oncogene. 2001 Apr 19;20(17):2161-70. doi: 10.1038/sj.onc.1204289. Oncogene. 2001. PMID: 11360200

8

Mutation and deletion analysis of GFR alpha-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumours.

Gimm O, Gössling A, Marsh DJ, Dahia PL, Mulligan LM, von Deimling A, Eng C. Gimm O, et al. Br J Cancer. 1999 May;80(3-4):383-6. doi: 10.1038/sj.bjc.6690367. Br J Cancer. 1999. PMID: 10408842 Free PMC article.

9

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation.

Gimm O, Marsh DJ, Andrew SD, Frilling A, Dahia PL, Mulligan LM, Zajac JD, Robinson BG, Eng C. Gimm O, et al. J Clin Endocrinol Metab. 1997 Nov;82(11):3902-4. doi: 10.1210/jcem.82.11.4508. J Clin Endocrinol Metab. 1997. PMID: 9360560

10

Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation.

Gimm O, Neuberg DS, Marsh DJ, Dahia PL, Hoang-Vu C, Raue F, Hinze R, Dralle H, Eng C. Gimm O, et al. Oncogene. 1999 Feb 11;18(6):1369-73. doi: 10.1038/sj.onc.1202418. Oncogene. 1999. PMID: 10022819

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