202 related articles for article (PubMed ID: 28938470)
1. Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia.
Eachus H; Zaucker A; Oakes JA; Griffin A; Weger M; Güran T; Taylor A; Harris A; Greenfield A; Quanson JL; Storbeck KH; Cunliffe VT; Müller F; Krone N
Endocrinology; 2017 Dec; 158(12):4165-4173. PubMed ID: 28938470
[TBL] [Abstract][Full Text] [Related]
2. Genetic Disruption of
Carranza J; Yamada K; Sakae Y; Noh J; Choi MH; Tanaka M
Zoolog Sci; 2024 Jun; 41(3):263-274. PubMed ID: 38809865
[No Abstract] [Full Text] [Related]
3. Ferredoxin 1b (Fdx1b) Is the Essential Mitochondrial Redox Partner for Cortisol Biosynthesis in Zebrafish.
Griffin A; Parajes S; Weger M; Zaucker A; Taylor AE; O'Neil DM; Müller F; Krone N
Endocrinology; 2016 Mar; 157(3):1122-34. PubMed ID: 26650568
[TBL] [Abstract][Full Text] [Related]
4. Redefining the initiation and maintenance of zebrafish interrenal steroidogenesis by characterizing the key enzyme cyp11a2.
Parajes S; Griffin A; Taylor AE; Rose IT; Miguel-Escalada I; Hadzhiev Y; Arlt W; Shackleton C; Müller F; Krone N
Endocrinology; 2013 Aug; 154(8):2702-11. PubMed ID: 23671259
[TBL] [Abstract][Full Text] [Related]
5. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Coeli-Lacchini FB; Turatti W; Elias PC; Elias LL; Martinelli CE; Moreira AC; Antonini SR; de Castro M
Gene; 2013 Sep; 526(2):239-45. PubMed ID: 23570880
[TBL] [Abstract][Full Text] [Related]
6. Identification of CYP21A2 mutant alleles in Czech patients with 21-hydroxylase deficiency.
Vrzalová Z; Hrubá Z; St'ahlová Hrabincová E; Pouchlá S; Votava F; Kolousková S; Fajkusová L
Int J Mol Med; 2010 Oct; 26(4):595-603. PubMed ID: 20818501
[TBL] [Abstract][Full Text] [Related]
7. Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree.
Liu J; Zhang X; Zhang H; Fang L; Xu J; Guan Q; Xu C
Mol Med Rep; 2018 Mar; 17(3):4265-4272. PubMed ID: 29328376
[TBL] [Abstract][Full Text] [Related]
8. Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation.
Toraman B; Ökten A; Kalay E; Karagüzel G; Dinçer T; Açıkgöz EG; Karagüzel A
Gene; 2013 Jan; 513(1):202-8. PubMed ID: 23142378
[TBL] [Abstract][Full Text] [Related]
9. Expression and activity profiling of the steroidogenic enzymes of glucocorticoid biosynthesis and the fdx1 co-factors in zebrafish.
Weger M; Diotel N; Weger BD; Beil T; Zaucker A; Eachus HL; Oakes JA; do Rego JL; Storbeck KH; Gut P; Strähle U; Rastegar S; Müller F; Krone N
J Neuroendocrinol; 2018 Apr; 30(4):e12586. PubMed ID: 29486070
[TBL] [Abstract][Full Text] [Related]
10. Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations.
Concolino P; Mello E; Zuppi C; Capoluongo E
Clin Chem Lab Med; 2010 Aug; 48(8):1057-62. PubMed ID: 20482300
[TBL] [Abstract][Full Text] [Related]
11. Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.
Dumic KK; Grubic Z; Yuen T; Wilson RC; Kusec V; Barisic I; Stingl K; Sansovic I; Skrabic V; Dumic M; New MI
J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):51-56. PubMed ID: 27041116
[TBL] [Abstract][Full Text] [Related]
12. Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.
Lekarev O; Tafuri K; Lane AH; Zhu G; Nakamoto JM; Buller-Burckle AM; Wilson TA; New MI
J Perinatol; 2013 Jan; 33(1):76-8. PubMed ID: 23269230
[TBL] [Abstract][Full Text] [Related]
13. Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia.
Vrzalová Z; Hrubá Z; Hrabincová ES; Vrábelová S; Votava F; Koloušková S; Fajkusová L
Eur J Med Genet; 2011; 54(2):112-7. PubMed ID: 20970527
[TBL] [Abstract][Full Text] [Related]
14. Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene.
Concolino P; Costella A
Mol Diagn Ther; 2018 Jun; 22(3):261-280. PubMed ID: 29450859
[TBL] [Abstract][Full Text] [Related]
15. 21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification.
Turan I; Tastan M; Boga DD; Gurbuz F; Kotan LD; Tuli A; Yüksel B
Eur J Med Genet; 2020 Apr; 63(4):103782. PubMed ID: 31586465
[TBL] [Abstract][Full Text] [Related]
16. Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling.
Kor Y; Zou M; Al-Rijjal RA; Monies D; Meyer BF; Shi Y
BMC Med Genet; 2018 Jul; 19(1):115. PubMed ID: 29996815
[TBL] [Abstract][Full Text] [Related]
17. A simple and robust quantitative PCR assay to determine CYP21A2 gene dose in the diagnosis of 21-hydroxylase deficiency.
Parajes S; Quinterio C; Domínguez F; Loidi L
Clin Chem; 2007 Sep; 53(9):1577-84. PubMed ID: 17634211
[TBL] [Abstract][Full Text] [Related]
18. Aberrant Global and Jagged-Mediated Notch Signaling Disrupts Segregation Between wt1-Expressing and Steroidogenic Tissues in Zebrafish.
Chou CW; Lin J; Jiang YJ; Liu YW
Endocrinology; 2017 Dec; 158(12):4206-4217. PubMed ID: 29029162
[TBL] [Abstract][Full Text] [Related]
19. Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
Parsa AA; New MI
J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):2-11. PubMed ID: 27380651
[TBL] [Abstract][Full Text] [Related]
20. High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.
Parajes S; Quinteiro C; Domínguez F; Loidi L
PLoS One; 2008 May; 3(5):e2138. PubMed ID: 18478071
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]