Karoly Racz
Affiliations: | Semmelweis Egyetem, Hungary |
Area:
Physiology Biology, BiochemistryGoogle:
"Karoly Racz"Mean distance: (not calculated yet)
Children
Sign in to add trainee| Attila Patocs | grad student | 2004 | Semmelweis Egyetem |
| Nikolette Szucs | grad student | 2005 | Semmelweis Egyetem |
| Zita Halasz | grad student | 2007 | Semmelweis Egyetem |
| Rita Bertalan | grad student | 2009 | Semmelweis Egyetem |
| Agnes E. Sallai | grad student | 2009 | Semmelweis Egyetem |
| Henriett Butz | grad student | 2010 | Semmelweis Egyetem |
| Zsofia Tombol | grad student | 2011 | Semmelweis Egyetem |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Marczell I, Balogh P, Nyiro G, et al. (2018) Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells. European Journal of Medical Research. 23: 31 |
| Molnár Á, Patócs A, Likó I, et al. (2018) An unexpected, mild phenotype of glucocorticoid resistance associated with glucocorticoid receptor gene mutation case report and review of the literature. Bmc Medical Genetics. 19: 37 |
| Darvasi O, Szabo PM, Nemeth K, et al. (2017) Limitations of high throughput methods for miRNA expression profiles in non-functioning pituitary adenomas. Pathology Oncology Research : Por |
| Mészáros K, Karvaly G, Márta Z, et al. (2017) Diagnostic performance of a newly developed salivary cortisol and cortisone measurement using an LC-MS/MS method with simple and rapid sample preparation. Journal of Endocrinological Investigation |
| Grolmusz VK, Borka K, Kövesdi A, et al. (2017) MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism. Virchows Archiv : An International Journal of Pathology |
| Doleschall M, Luczay A, Koncz K, et al. (2017) A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics. European Journal of Human Genetics : Ejhg |
| Bausch B, Schiavi F, Ni Y, et al. (2017) Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention. Jama Oncology |
| Butz H, Németh K, Czenke D, et al. (2016) Systematic Investigation of Expression of G2/M Transition Genes Reveals CDC25 Alteration in Nonfunctioning Pituitary Adenomas. Pathology Oncology Research : Por |
| Grolmusz VK, Karászi K, Micsik T, et al. (2016) Cell cycle dependent RRM2 may serve as proliferation marker and pharmaceutical target in adrenocortical cancer. American Journal of Cancer Research. 6: 2041-2053 |
| Nagy Z, Marta A, Butz H, et al. (2016) Modulation of the circadian clock by glucocorticoid receptor isoforms in the H295R cell line. Steroids |