메뉴 건너뛰기




Volumn 152, Issue 12, 2011, Pages 4478-4480

Hear, hear! thyroid hormone transporters in cochlear development

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID TRANSPORTER; COTRANSPORTER; LAT1 PROTEIN; LAT2 PROTEIN; LIOTHYRONINE; MONOCARBOYXLATE TRANSPORTER 10; MONOCARBOYXLATE TRANSPORTER 8; ORGANIC ANION TRANSPORTER 1; OXIDOREDUCTASE; THYROID HORMONE; THYROID HORMONE RECEPTOR; THYROXINE; TYPE 2 DEIODINASE; TYPE 3 DEIODINASE; UNCLASSIFIED DRUG;

EID: 82355188238     PISSN: 00137227     EISSN: 19457170     Source Type: Journal    
DOI: 10.1210/en.2011-1722     Document Type: Short Survey
Times cited : (9)

References (29)
  • 1
    • 82355188204 scopus 로고    scopus 로고
    • Developmental and cell-specific expression of thyroid hormone transporters in the mouse cochlea
    • Sharlin DS, Visser TJ, Forrest D 2011 Developmental and cell-specific expression of thyroid hormone transporters in the mouse cochlea. Endocrinology 152:5053-5064
    • (2011) Endocrinology , vol.152 , pp. 5053-5064
    • Sharlin, D.S.1    Visser, T.J.2    Forrest, D.3
  • 3
    • 0029892866 scopus 로고    scopus 로고
    • Long-term sequelae of hearing impairment in congenital hypothyroidism
    • DOI 10.1016/S0022-3476(96)70329-3
    • Rovet J, Walker W, Bliss B, Buchanan L, Ehrlich R 1996 Long-term sequelae of hearing impairment in congenital hypothyroidism. J Pediatr 128:776-783 (Pubitemid 26181374)
    • (1996) Journal of Pediatrics , vol.128 , Issue.6 , pp. 776-783
    • Rovet, J.1    Walker, W.2    Bliss, B.3    Buchanan, L.4    Ehrlich, R.5
  • 5
    • 0014055213 scopus 로고
    • Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: Possible target organ refractoriness to thyroid hormone
    • Refetoff S, DeWind LT, DeGroot LJ 1967 Familial syndrome combining deaf-mutism, stuppled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone. J Clin Endocrinol Metab 27:279-294
    • (1967) J Clin Endocrinol Metab , vol.27 , pp. 279-294
    • Refetoff, S.1    DeWind, L.T.2    DeGroot, L.J.3
  • 8
    • 63849159901 scopus 로고    scopus 로고
    • A protective role for type 3 deiodinase, a thyroid hormone-inactivating enzyme, in cochlear development and auditory function
    • Ng L, Hernandez A, He W, Ren T, Srinivas M, Ma M, Galton VA, St Germain DL, Forrest D 2009 A protective role for type 3 deiodinase, a thyroid hormone-inactivating enzyme, in cochlear development and auditory function. Endocrinology 150:1952-1960
    • (2009) Endocrinology , vol.150 , pp. 1952-1960
    • Ng, L.1    Hernandez, A.2    He, W.3    Ren, T.4    Srinivas, M.5    Ma, M.6    Galton, V.A.7    St Germain, D.L.8    Forrest, D.9
  • 10
    • 0029947835 scopus 로고    scopus 로고
    • Thyroid hormone receptor beta is essential for development of auditory function
    • DOI 10.1038/ng0796-354
    • Forrest D, Erway LC, Ng L, Altschuler R, Curran T 1996 Thyroid hormone receptor beta is essential for development of auditory function. Nat Genet 13:354-357 (Pubitemid 26230504)
    • (1996) Nature Genetics , vol.13 , Issue.3 , pp. 354-357
    • Forrest, D.1    Erway, L.C.2    Ng, L.3    Altschuler, R.4    Curran, T.5
  • 12
    • 33747590148 scopus 로고    scopus 로고
    • Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (Mct) 8-deficient mice
    • DOI 10.1210/en.2006-0390
    • Dumitrescu AM, Liao XH, Weiss RE, Millen K, Refetoff S 2006 Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice. Endocrinology 147:4036-4043 (Pubitemid 44268357)
    • (2006) Endocrinology , vol.147 , Issue.9 , pp. 4036-4043
    • Dumitrescu, A.M.1    Liao, X.-H.2    Weiss, R.E.3    Millen, K.4    Refetoff, S.5
  • 15
    • 0347634343 scopus 로고    scopus 로고
    • A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene
    • DOI 10.1086/380999
    • Dumitrescu AM, Liao XH, Best TB, Brockmann K, Refetoff S 2004 A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene. Am J Hum Genet 74:168-175 (Pubitemid 38085248)
    • (2004) American Journal of Human Genetics , vol.74 , Issue.1 , pp. 168-175
    • Dumitrescu, A.M.1    Liao, X.-H.2    Best, T.B.3    Brockmann, K.4    Refetoff, S.5
  • 18
    • 0242384851 scopus 로고    scopus 로고
    • Functional Characterization of Rat Brain-specific Organic Anion Transporter (Oatp14) at the Blood-Brain Barrier: High affinity transporter for thyroxine
    • DOI 10.1074/jbc.M306933200
    • Sugiyama D, Kusuhara H, Taniguchi H, Ishikawa S, Nozaki Y, Aburatani H, Sugiyama Y 2003 Functional characterization of rat brain-specific organic anion transporter (Oatp14) at the bloodbrain barrier: high affinity transporter for thyroxine. J Biol Chem 278:43489-43495 (Pubitemid 37345972)
    • (2003) Journal of Biological Chemistry , vol.278 , Issue.44 , pp. 43489-43495
    • Sugiyama, D.1    Kusuhara, H.2    Taniguchi, H.3    Ishikawa, S.4    Nozaki, Y.5    Aburatani, H.6    Sugiyama, Y.7
  • 20
    • 78650916392 scopus 로고    scopus 로고
    • Thyroid hormone transporters: The knowns and the unknowns
    • Visser WE, Friesema EC, Visser TJ 2011 Thyroid hormone transporters: the knowns and the unknowns. Mol Endocrinol 25:1-14
    • (2011) Mol Endocrinol , vol.25 , pp. 1-14
    • Visser, W.E.1    Friesema, E.C.2    Visser, T.J.3
  • 21
    • 0030786397 scopus 로고    scopus 로고
    • Regional distribution of type 2 thyroxine deiodinase messenger ribonucleic acid in rat hypothalamus and pituitary and its regulation by thyroid hormone
    • DOI 10.1210/en.138.8.3359
    • Tu HM, Kim SW, Salvatore D, Bartha T, Legradi G, Larsen PR, Lechan RM 1997 Regional distribution of type 2 thyroxine deiodinase messenger ribonucleic acid in rat hypothalamus and pituitary and its regulation by thyroid hormone. Endocrinology 138:3359-3368 (Pubitemid 27345689)
    • (1997) Endocrinology , vol.138 , Issue.8 , pp. 3359-3368
    • Tu, H.M.1    Kim, S.-W.2    Salvatore, D.3    Bartha, T.4    Legradi, G.5    Larsen, P.R.6    Lechan, R.M.7
  • 26
  • 29
    • 33646162906 scopus 로고    scopus 로고
    • The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23
    • Ali G, Santos RL, John P, Wambangco MA, Lee K, Ahmad W, Leal S 2006 The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23. Clin Genet 69:429-433
    • (2006) Clin Genet , vol.69 , pp. 429-433
    • Ali, G.1    Santos, R.L.2    John, P.3    Wambangco, M.A.4    Lee, K.5    Ahmad, W.6    Leal, S.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.