Rácz K - Search Results

1

MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism.

Grolmusz VK, Borka K, Kövesdi A, Németh K, Balogh K, Dékány C, Kiss A, Szentpéteri A, Sármán B, Somogyi A, Csajbók É, Valkusz Z, Tóth M, Igaz P, Rácz K, Patócs A. Grolmusz VK, et al. Among authors: racz k. Virchows Arch. 2017 Sep;471(3):401-411. doi: 10.1007/s00428-017-2158-3. Epub 2017 Jun 8. Virchows Arch. 2017. PMID: 28597079

2

Menin and its interacting proteins: elucidation of menin function.

Balogh K, Rácz K, Patócs A, Hunyady L. Balogh K, et al. Among authors: racz k. Trends Endocrinol Metab. 2006 Nov;17(9):357-64. doi: 10.1016/j.tem.2006.09.004. Epub 2006 Sep 25. Trends Endocrinol Metab. 2006. PMID: 16997566 Review.

3

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.

Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K. Balogh K, et al. Among authors: racz k. Clin Endocrinol (Oxf). 2007 Nov;67(5):727-34. doi: 10.1111/j.1365-2265.2007.02953.x. Clin Endocrinol (Oxf). 2007. PMID: 17953629

4

Adrenal tumors in MEN1 syndrome and the role of menin in adrenal tumorigenesis.

Patocs A, Balogh K, Racz K. Patocs A, et al. Among authors: racz k. Adv Exp Med Biol. 2009;668:97-103. doi: 10.1007/978-1-4419-1664-8_10. Adv Exp Med Biol. 2009. PMID: 20175457 Review. No abstract available.

5

Menin dynamics and functional insight: take your partners.

Balogh K, Patócs A, Hunyady L, Rácz K. Balogh K, et al. Among authors: racz k. Mol Cell Endocrinol. 2010 Sep 15;326(1-2):80-4. doi: 10.1016/j.mce.2010.04.011. Epub 2010 Apr 24. Mol Cell Endocrinol. 2010. PMID: 20399832 Review.

6

Unusual presentation of multiple endocrine neoplasia type 1 in a young woman with a novel mutation of the MEN1 gene.

Balogh K, Patócs A, Majnik J, Varga F, Illyés G, Hunyady L, Rácz K. Balogh K, et al. Among authors: racz k. J Hum Genet. 2004;49(7):380-386. doi: 10.1007/s10038-004-0163-2. Epub 2004 Jun 16. J Hum Genet. 2004. PMID: 15205994

7

Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1.

Balogh K, Patócs A, Majnik J, Rácz K, Hunyady L. Balogh K, et al. Among authors: racz k. Mol Genet Metab. 2004 Sep-Oct;83(1-2):74-81. doi: 10.1016/j.ymgme.2004.08.013. Mol Genet Metab. 2004. PMID: 15464422 Review.

8

Parathyroid hormone-dependent hypercalcemia.

Toke J, Patócs A, Balogh K, Gergics P, Stenczer B, Rácz K, Tóth M. Toke J, et al. Among authors: racz k. Wien Klin Wochenschr. 2009;121(7-8):236-45. doi: 10.1007/s00508-009-1149-z. Wien Klin Wochenschr. 2009. PMID: 19562279 Review.

9

Differences in the expression of histamine-related genes and proteins in normal human adrenal cortex and adrenocortical tumors.

Szabó PM, Wiener Z, Tömböl Z, Kovács A, Pócza P, Horányi J, Kulka J, Riesz P, Tóth M, Patócs A, Gaillard RC, Falus A, Rácz K, Igaz P. Szabó PM, et al. Among authors: racz k. Virchows Arch. 2009 Aug;455(2):133-42. doi: 10.1007/s00428-009-0807-x. Epub 2009 Jul 1. Virchows Arch. 2009. PMID: 19568768

10

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: racz k. 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

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