메뉴 건너뛰기




Volumn 45, Issue , 1996, Pages 25-28

Pit-1: Clinical aspects

Author keywords

Growth hormone deficiency; Hypothyroidism; Mutation; Pit 1; Pit 1 GHF 1; Pituitary gland; Pituitary hormone deficiency

Indexed keywords

GROWTH HORMONE; HYPOPHYSIS HORMONE; PROLACTIN; THYROTROPIN; TRANSCRIPTION FACTOR PIT 1;

EID: 0029979942     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000184824     Document Type: Article
Times cited : (49)

References (10)
  • 1
    • 0000706712 scopus 로고
    • The pituitary-specific transcription factor GHF-1 is a homcobox-con-taining protein
    • Bodncr M, Castrillo JL, Theill LE, Dccrink T, Ellismann M, Karin M: The pituitary-specific transcription factor GHF-1 is a homcobox-con-taining protein. Cell 1988;55:267-275.
    • (1988) Cell , vol.55 , pp. 267-275
    • Bodncr, M.1    Castrillo, J.L.2    Theill, L.E.3    Dccrink, T.4    Ellismann, M.5    Karin, M.6
  • 4
    • 0026767630 scopus 로고
    • Wein-traub BD, Wondisford FE: A mutation in the POU-homcodomain of Pit-1 responsible for combined pituitary hormone deficienc
    • Radovick S, Nations M. Du Y. Berg LA. Wein-traub BD, Wondisford FE: A mutation in the POU-homcodomain of Pit-1 responsible for combined pituitary hormone deficiency. Science 1992;257:1115-1118.
    • (1992) Science , vol.25 , pp. 1115-2111
    • Radovick, S.1    Nations, M.D.2    Berg, Y.L.A.3
  • 7
    • 0343460423 scopus 로고
    • A genetic cause of familial and sporadic cases with combined pituitary hormone deficiencies for GH, Prl and TSH
    • abstract
    • Pfäffle RW, Olten B, Eiholzcr U, Kim C, Blankenstein O: A genetic cause of familial and sporadic cases with combined pituitary hormone deficiencies for GH, Prl and TSH. Horm Res 1995:44:9 (abstract).
    • (1995) Horm Res , vol.44 , pp. 9
    • Pfäffle, R.W.1    Olten, B.2    Eiholzcr, U.3    Kim, C.4    Blankenstein, O.5
  • 9
    • 0029121819 scopus 로고
    • A novel F.250X mutation of the Pit-1 gene in a patient with combined pituitary hormone deficiency
    • Irie Y, Tatsumi K, Ogawa M, Kamijo T, Precvasombat C, Suprasongsin C, Amin N: A novel F.250X mutation of the Pit-1 gene in a patient with combined pituitary hormone deficiency. EndocrJ 1995;42:351-354.
    • (1995) Endocrj , vol.42 , pp. 351-354
    • Irie, Y.1    Tatsumi, K.2    Ogawa, M.3    Kamijo, T.4    Precvasombat, C.5    Suprasongsin, C.6    Amin, N.7
  • 10
    • 0027980595 scopus 로고
    • Monoallelic expression of normal mRNA in the Pit-1 mutation licterozygotes with normal phenotype and biallclic expression in the abnormal phenotype
    • Okamoto N, Wada Y, Ida S, Koga R, Ozono K, Chiyo H, Hayashi A, Tatsumi K: Monoallelic expression of normal mRNA in the Pit-1 mutation licterozygotes with normal phenotype and biallclic expression in the abnormal phenotype. Hum Mol Genet 1994:3:1565-1568.
    • (1994) Hum Mol Genet , vol.3 , pp. 1565-1568
    • Okamoto, N.1    Wada, Y.2    Ida, S.3    Koga, R.4    Ozono, K.5    Chiyo, H.6    Hayashi, A.7    Tatsumi, K.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.