Likó I - Search Results

1

Germline BRCA1 Mutation Detected in a Multiple Endocrine Neoplasia Type 2 Case With RET Codon 634 Mutation.

Sarkadi B, Baghy K, Sápi Z, Nyirő G, Likó I, Patócs A. Sarkadi B, et al. Among authors: liko i. Front Genet. 2019 Jun 11;10:544. doi: 10.3389/fgene.2019.00544. eCollection 2019. Front Genet. 2019. PMID: 31263477 Free PMC article.

2

Sequence variants of the ligand-binding domain of the glucocorticoid receptor gene and their functional consequences on the three-dimensional protein structure.

Likó I, Igaz P, Patócs A, Tóth S, Pázmány T, Tóth M, Rácz K. Likó I, et al. Curr Med Chem. 2004 Dec;11(24):3229-37. doi: 10.2174/0929867043363749. Curr Med Chem. 2004. PMID: 15579010 Review.

3

Gene symbol: CYP17A1. Disease: Steroid 17-alpha-hydrolylase deficiency.

Patocs AP, Liko I, Racz K. Patocs AP, et al. Among authors: liko i. Hum Genet. 2005 May;116(6):539. Hum Genet. 2005. PMID: 15991317 No abstract available.

4

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

Patocs A, Liko I, Varga I, Gergics P, Boros A, Futo L, Kun I, Bertalan R, Toth S, Pazmany T, Toth M, Szücs N, Horanyi J, Glaz E, Racz K. Patocs A, et al. Among authors: liko i. J Steroid Biochem Mol Biol. 2005 Nov;97(3):257-65. doi: 10.1016/j.jsbmb.2005.06.035. Epub 2005 Sep 19. J Steroid Biochem Mol Biol. 2005. PMID: 16176874

5

Polymorphisms of the glucocorticoid receptor gene in Graves ophthalmopathy.

Boyle B, Korányi K, Patocs A, Liko I, Szappanos A, Bertalan R, Racz K, Balazs C. Boyle B, et al. Among authors: liko i. Br J Ophthalmol. 2008 Jan;92(1):131-4. doi: 10.1136/bjo.2007.126789. Br J Ophthalmol. 2008. PMID: 18156379

6

Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family.

Patocs A, Gergics P, Balogh K, Toth M, Fazakas F, Liko I, Racz K. Patocs A, et al. Among authors: liko i. BMC Med Genet. 2008 Apr 16;9:29. doi: 10.1186/1471-2350-9-29. BMC Med Genet. 2008. PMID: 18416845 Free PMC article.

7

BclI polymorphism of the glucocorticoid receptor gene is associated with decreased bone mineral density in patients with endogenous hypercortisolism.

Szappanos A, Patócs A, Tõke J, Boyle B, Sereg M, Majnik J, Borgulya G, Varga I, Likó I, Rácz K, Tóth M. Szappanos A, et al. Among authors: liko i. Clin Endocrinol (Oxf). 2009 Nov;71(5):636-43. doi: 10.1111/j.1365-2265.2009.03528.x. Epub 2009 Jan 22. Clin Endocrinol (Oxf). 2009. PMID: 19207316

8

Integrative molecular bioinformatics study of human adrenocortical tumors: microRNA, tissue-specific target prediction, and pathway analysis.

Tömböl Z, Szabó PM, Molnár V, Wiener Z, Tölgyesi G, Horányi J, Riesz P, Reismann P, Patócs A, Likó I, Gaillard RC, Falus A, Rácz K, Igaz P. Tömböl Z, et al. Among authors: liko i. Endocr Relat Cancer. 2009 Sep;16(3):895-906. doi: 10.1677/ERC-09-0096. Epub 2009 Jun 22. Endocr Relat Cancer. 2009. PMID: 19546168

9

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I, Fazakas F, Szabo I, Kovacs B, Glaz E, Racz K. Gergics P, et al. Among authors: liko i. Eur J Endocrinol. 2009 Sep;161(3):495-502. doi: 10.1530/EJE-09-0399. Epub 2009 Jul 2. Eur J Endocrinol. 2009. PMID: 19574279

10

Pharmacological options for treatment of hyperandrogenic disorders.

Reismann P, Likó I, Igaz P, Patócs A, Rácz K. Reismann P, et al. Among authors: liko i. Mini Rev Med Chem. 2009 Aug;9(9):1113-26. doi: 10.2174/138955709788922692. Mini Rev Med Chem. 2009. PMID: 19689407 Review.

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