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2. OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary. Tajima T, Ohtake A, Hoshino M, Amemiya S, Sasaki N, Ishizu K, Fujieda K. J Clin Endocrinol Metab; 2009 Jan; 94(1):314-9. PubMed ID: 18854396 [Abstract] [Full Text] [Related]
3. Congenital pituitary hypoplasia model demonstrates hypothalamic OTX2 regulation of pituitary progenitor cells. Matsumoto R, Suga H, Aoi T, Bando H, Fukuoka H, Iguchi G, Narumi S, Hasegawa T, Muguruma K, Ogawa W, Takahashi Y. J Clin Invest; 2020 Feb 03; 130(2):641-654. PubMed ID: 31845906 [Abstract] [Full Text] [Related]
13. A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency. Diaczok D, Romero C, Zunich J, Marshall I, Radovick S. J Clin Endocrinol Metab; 2008 Nov 03; 93(11):4351-9. PubMed ID: 18728160 [Abstract] [Full Text] [Related]
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16. OTX1 compensates for OTX2 requirement in regionalisation of anterior neuroectoderm. Acampora D, Annino A, Puelles E, Alfano I, Tuorto F, Simeone A. Gene Expr Patterns; 2003 Aug 03; 3(4):497-501. PubMed ID: 12915318 [Abstract] [Full Text] [Related]
17. The phenotypic spectrum associated with OTX2 mutations in humans. Gregory LC, Gergics P, Nakaguma M, Bando H, Patti G, McCabe MJ, Fang Q, Ma Q, Ozel AB, Li JZ, Poina MM, Jorge AAL, Benedetti AFF, Lerario AM, Arnhold IJP, Mendonca BB, Maghnie M, Camper SA, Carvalho LRS, Dattani MT. Eur J Endocrinol; 2021 May 25; 185(1):121-135. PubMed ID: 33950863 [Abstract] [Full Text] [Related]
18. Regulation of Otx2 expression and its functions in mouse epiblast and anterior neuroectoderm. Kurokawa D, Takasaki N, Kiyonari H, Nakayama R, Kimura-Yoshida C, Matsuo I, Aizawa S. Development; 2004 Jul 25; 131(14):3307-17. PubMed ID: 15201223 [Abstract] [Full Text] [Related]