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8. Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia. Cohen RN; Cohen LE; Botero D; Yu C; Sagar A; Jurkiewicz M; Radovick S J Clin Endocrinol Metab; 2003 Oct; 88(10):4832-9. PubMed ID: 14557462 [TBL] [Abstract][Full Text] [Related]
9. HESX1: a novel gene implicated in a familial form of septo-optic dysplasia. Dattani MT; Martinez-Barbera JP; Thomas PQ; Brickman JM; Gupta R; Wales JK; Hindmarsh PC; Beddington RS; Robinson IC Acta Paediatr Suppl; 1999 Dec; 88(433):49-54. PubMed ID: 10626545 [TBL] [Abstract][Full Text] [Related]
10. Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia. Corneli G; Vivenza D; Prodam F; Di Dio G; Vottero A; Rapa A; Bellone S; Bernasconi S; Bona G J Endocrinol Invest; 2008 Aug; 31(8):689-93. PubMed ID: 18852528 [TBL] [Abstract][Full Text] [Related]
11. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse. Dattani MT; Martinez-Barbera JP; Thomas PQ; Brickman JM; Gupta R; Mårtensson IL; Toresson H; Fox M; Wales JK; Hindmarsh PC; Krauss S; Beddington RS; Robinson IC Nat Genet; 1998 Jun; 19(2):125-33. PubMed ID: 9620767 [TBL] [Abstract][Full Text] [Related]
12. A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes. Takagi M; Takahashi M; Ohtsu Y; Sato T; Narumi S; Arakawa H; Hasegawa T Endocr J; 2016 Apr; 63(4):405-10. PubMed ID: 26781211 [TBL] [Abstract][Full Text] [Related]
13. Septo-optic dysplasia and other midline defects: the role of transcription factors: HESX1 and beyond. McCabe MJ; Alatzoglou KS; Dattani MT Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):115-24. PubMed ID: 21396578 [TBL] [Abstract][Full Text] [Related]
14. Molecular genetics of septo-optic dysplasia. Dattani ML; Martinez-Barbera J; Thomas PQ; Brickman JM; Gupta R; Wales JK; Hindmarsh PC; Beddington RS; Robinson IC Horm Res; 2000; 53 Suppl 1():26-33. PubMed ID: 10895039 [TBL] [Abstract][Full Text] [Related]
15. Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient. Tajima T; Hattorri T; Nakajima T; Okuhara K; Sato K; Abe S; Nakae J; Fujieda K J Clin Endocrinol Metab; 2003 Jan; 88(1):45-50. PubMed ID: 12519827 [TBL] [Abstract][Full Text] [Related]
16. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency. Avbelj Stefanija M; Kotnik P; Bratanič N; Žerjav Tanšek M; Bertok S; Bratina N; Battelino T; Trebušak Podkrajšek K Horm Res Paediatr; 2015; 84(3):153-8. PubMed ID: 26111865 [TBL] [Abstract][Full Text] [Related]
17. Disruption of SoxB1-dependent Sonic hedgehog expression in the hypothalamus causes septo-optic dysplasia. Zhao L; Zevallos SE; Rizzoti K; Jeong Y; Lovell-Badge R; Epstein DJ Dev Cell; 2012 Mar; 22(3):585-96. PubMed ID: 22421044 [TBL] [Abstract][Full Text] [Related]
18. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia. Rainbow LA; Rees SA; Shaikh MG; Shaw NJ; Cole T; Barrett TG; Kirk JM Clin Endocrinol (Oxf); 2005 Feb; 62(2):163-8. PubMed ID: 15670191 [TBL] [Abstract][Full Text] [Related]