Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rita Bertalan"'
Autor:
Caroline Eozenou, David Rodriguez-Buritica, Zita Halász, Jean-Pierre Siffroi, Joelle Bignon-Topalovic, Anne Jorgensen, Sophie Lambert, Rajpert-De Meyts E, János Sólyom, Anu Bashamboo, Ken McElreavey, Paye-Jaouen A, Rita Bertalan, Attila Tar, Capucine Hyon, John C. Achermann, Peter Nagy, Laetitia Martinerie
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2018, 102 (3), pp.487-493. ⟨10.1016/j.ajhg.2018.01.021⟩
American Journal of Human Genetics, 2018, 102 (3), pp.487-493. ⟨10.1016/j.ajhg.2018.01.021⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2018, 102 (3), pp.487-493. ⟨10.1016/j.ajhg.2018.01.021⟩
American Journal of Human Genetics, 2018, 102 (3), pp.487-493. ⟨10.1016/j.ajhg.2018.01.021⟩
International audience; Emerging evidence from murine studies suggests that mammalian sex determination is the outcome of an imbalance between mutually antagonistic male and female regulatory networks that canalize development down one pathway while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e91d6a53f3d8867c6d02692f0689a27
https://hal-pasteur.archives-ouvertes.fr/pasteur-02872425
https://hal-pasteur.archives-ouvertes.fr/pasteur-02872425
Autor:
Imre Zoltan Kun, Károly Rácz, Ibolya Varga, Tamas Pazmany, László Futo, Andras Boros, Szilvia Toth, Rita Bertalan, István Likó, Nikolette Szücs, Edit Gláz, Peter Gergics, Attila Patócs, Miklós Tóth, János Horányi
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 97:257-265
The CYP17 gene, located on chromosome 10q24-q25, encodes the cytochrome P450c17 enzyme. Mutations of this gene cause the 17alpha-hydroxylase/17,20-lyase deficiency, which is a rare, autosomal recessive form of congenital adrenal hyperplasia. Approxim
Autor:
Attila Patócs, Miklós Tóth, Judit Toke, Rita Bertalan, Zsolt Tulassay, Károly Rácz, Peter Gergics
Publikováno v:
Orvosi hetilap. 150(17)
Ionic calcium has been known as an important intracellular second messenger for many decades. In addition, a whole series of experimental and clinical studies from the past fifteen years have provided evidence that extracellular ionic calcium itself
Autor:
Zita Halász, Attila Patócs, Rita Bertalan, Judit Tőke, János Sólyom, László Kovács, Ágnes Sallai, Károly Rácz, Ágota Muzsnai, Zsófia Tömböl, Éva Hosszú, György Fekete
Publikováno v:
Endocrine. 30(3)
Combined pituitary hormone deficiency is characterized by the impaired production of pituitary hormones, commonly including growth hormone. The pathomechanism of the childhood-onset form of this disorder may involve germline mutations of genes encodi