Marton Doleschall
Marton Doleschall
Molecular Medicine Research Group, HAS-SE, Hungary
Verified email at med.semmelweis-univ.hu
Title
Cited by
Cited by
Year
Lipopolysaccharide induces type 2 iodothyronine deiodinase in the mediobasal hypothalamus: implications for the nonthyroidal illness syndrome
C Fekete, B Gereben, M Doleschall, JW Harney, JM Dora, AC Bianco, ...
Endocrinology 145 (4), 1649-1655, 2004
1762004
Characterization of the Nuclear Factor-κB Responsiveness of the Human dio2 Gene
A Zeöld, M Doleschall, MC Haffner, LP Capelo, J Menyhért, Z Liposits, ...
Endocrinology 147 (9), 4419-4429, 2006
782006
Expression of the neonatal Fc receptor (FcRn) in the bovine mammary gland
B Mayer, M Doleschall, B Bender, J Bartyik, Z Bősze, LV Frenyó, ...
Journal of dairy research 72 (S1), 107-112, 2005
752005
Regulation of thyroid hormone activation via the liver X-receptor/retinoid X-receptor pathway
MA Christoffolete, M Doleschall, P Egri, Z Liposits, AM Zavacki, AC Bianco, ...
The Journal of endocrinology 205 (2), 179, 2010
352010
Cloning, expression and characterization of the bovine p65 subunit of NFκB
M Doleschall, B Mayer, J Cervenak, L Cervenak, I Kacskovics
Developmental & Comparative Immunology 31 (9), 945-961, 2007
292007
Fine-tuned characterization of RCCX copy number variants and their relationship with extended MHC haplotypes
Z Banlaki, M Doleschall, K Rajczy, G Fust, A Szilagyi
Genes & Immunity 13 (7), 530-535, 2012
252012
Isolation of the gene encoding the bovine neonatal Fc receptor
M Doleschall, Y Zhao, B Mayer, L Hammarström, I Kacskovics
Veterinary immunology and immunopathology 108 (1-2), 145-150, 2005
202005
ACTH‐induced cortisol release is related to the copy number of the C4B gene encoding the fourth component of complement in patients with non‐functional …
Z Bánlaki, G Raizer, B Ács, J Majnik, M Doleschall, Á Szilágyi, K Rácz, ...
Clinical endocrinology 76 (4), 478-484, 2012
132012
Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels
M Doleschall, JA Szabo, J Pazmandi, A Szilagyi, K Koncz, H Farkas, ...
PLoS One 9 (9), e107244, 2014
122014
Both positive and negative selection pressures contribute to the polymorphism pattern of the duplicated human CYP21A2 gene
JA Szabó, Á Szilágyi, Z Doleschall, A Patócs, H Farkas, Z Prohászka, ...
PloS one 8 (11), e81977, 2013
122013
Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene
Z Bánlaki, JA Szabó, Á Szilágyi, A Patócs, Z Prohászka, G Füst, ...
Genome biology and evolution 5 (1), 98-112, 2013
102013
NFκB induces overexpression of bovine FcRn: a novel mechanism that further contributes to the enhanced immune response in genetically modified animals carrying extra copies of FcRn
J Cervenak, M Doleschall, B Bender, B Mayer, Z Schneider, Z Doleschall, ...
mabs 5 (6), 860-871, 2013
92013
Increased thyroid hormone activation accompanies the formation of thyroid hormone-dependent negative feedback in developing chicken hypothalamus
P Mohácsik, T Füzesi, M Doleschall, A Szilvásy-Szabó, P Vancamp, ...
Endocrinology 157 (3), 1211-1221, 2016
62016
A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics
M Doleschall, A Luczay, K Koncz, K Hadzsiev, É Erhardt, Á Szilágyi, ...
European Journal of Human Genetics 25 (6), 702-710, 2017
42017
Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia
M Doleschall, D Török, K Mészáros, A Luczay, Z Halász, K Németh, ...
Orvosi hetilap 159 (7), 269, 2018
32018
Chromogranin A and its role in the pathogenesis of diabetes mellitus
Z Herold, M Doleschall, A Kovesdi, A Patocs, A Somogyi
Endokrynologia Polska 69 (5), 598-610, 2018
32018
Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin‐like cell hyperplasia and autoimmune …
Z Herold, M Herold, P Nagy, A Patocs, M Doleschall, A Somogyi
Journal of Diabetes Investigation, 2019
12019
Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka
M Doleschall, D Török, K Mészáros, A Luczay, Z Halász, K Németh, ...
Orvosi Hetilap 159 (7), 269-277, 2018
2018
Effects of the copy number of complement component 4 gene and the haplotypes of steroid 21-hydroxylase gene on hormone levels in patients with non-functioning adrenal adenoma: 219
M Doleschall, J Szabó, Z Bánlaki, Á Szilágyi, E Gláz, Z Prohászka, K Rácz, ...
European Journal of Clinical Investigation 42, 2012
2012
A központi idegrendszeri pajzsmirigyhormon aktiváció szabályozásának molekuláris biológiája= Molecular biology of the regulation of thyroid hormone activation in the central …
B Gereben, Z Bardóczi, M Doleschall, C Fekete, A Zeöld
OTKA Kutatási Jelentések| OTKA Research Reports, 2010
2010
The system can't perform the operation now. Try again later.
Articles 1–20