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Volumn 17, Issue 4, 2008, Pages 353-356

The development of the parathyroid gland: From fish to human

Author keywords

Fish; GATA3; Gcm2; Hypoparathyroidism; Parathyroid; Pax; Tbx1

Indexed keywords

CALCIUM; CHAPERONE; PAIRED BOX TRANSCRIPTION FACTOR; PARATHYROID HORMONE; T BOX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GATA 3; TUBULIN;

EID: 51949103456     PISSN: 10624821     EISSN: None     Source Type: Journal    
DOI: 10.1097/MNH.0b013e328304651c     Document Type: Review
Times cited : (33)

References (31)
  • 1
    • 0142027606 scopus 로고    scopus 로고
    • Identification of a parathyroid hormone in the fish Fugu rubripes
    • Danks JA, HoPM, Notini AJ, et al. Identification of a parathyroid hormone in the fish Fugu rubripes. J Bone Miner Res 2003; 18:1326-1331.
    • (2003) J Bone Miner Res , vol.18 , pp. 1326-1331
    • Danks, J.A.1    Ho, P.M.2    Notini, A.J.3
  • 2
    • 43149105569 scopus 로고    scopus 로고
    • McManus JF, Davey RA, MacLean HE. Intermittent Fugu parathyroid hormone 1 (1-34) is an anabolic bone agent in young male rats and osteopenic ovariectomized rats. Bone 2008; 13 Feb [Epub ahead of print].
    • McManus JF, Davey RA, MacLean HE. Intermittent Fugu parathyroid hormone 1 (1-34) is an anabolic bone agent in young male rats and osteopenic ovariectomized rats. Bone 2008; 13 Feb [Epub ahead of print].
  • 3
    • 33750842701 scopus 로고    scopus 로고
    • DiGeorge syndrome and pharyngeal apparatus development
    • Wurdak H, Ittner LM, Sommer L DiGeorge syndrome and pharyngeal apparatus development. Bioessays 2006; 28:1078-1086.
    • (2006) Bioessays , vol.28 , pp. 1078-1086
    • Wurdak, H.1    Ittner, L.M.2    Sommer, L.3
  • 4
    • 0842291537 scopus 로고    scopus 로고
    • GCMB: Another serendipitous gift from evolution to clinical investigators
    • Kronenberg HM. GCMB: another serendipitous gift from evolution to clinical investigators. J Clin Endocrinol Metab 2004; 89:6-7.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 6-7
    • Kronenberg, H.M.1
  • 5
    • 0034644149 scopus 로고    scopus 로고
    • Genetic ablation of parathyroid glands reveals another source of parathyroid hormone
    • Gunther T, Chen ZF, Kim J, et al. Genetic ablation of parathyroid glands reveals another source of parathyroid hormone. Nature 2000; 406:199-203.
    • (2000) Nature , vol.406 , pp. 199-203
    • Gunther, T.1    Chen, Z.F.2    Kim, J.3
  • 6
    • 34247149887 scopus 로고    scopus 로고
    • Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia
    • Liu Z, Yu S, Manley NR. Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordia. Dev Biol 2007; 305:333-346.
    • (2007) Dev Biol , vol.305 , pp. 333-346
    • Liu, Z.1    Yu, S.2    Manley, N.R.3
  • 7
    • 11144234118 scopus 로고    scopus 로고
    • The origin of the parathyroid gland
    • Okabe M, Graham A. The origin of the parathyroid gland. Proc Natl Acad Sci U S A 2004; 101:17716-17719.
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 17716-17719
    • Okabe, M.1    Graham, A.2
  • 8
    • 9944221652 scopus 로고    scopus 로고
    • Zebrafish gcm2 is required for gill filament budding from pharyngeal ectoderm
    • Hogan BM, Hunter MP, Oates AC, et al. Zebrafish gcm2 is required for gill filament budding from pharyngeal ectoderm. Dev Biol 2004; 276:508-522.
    • (2004) Dev Biol , vol.276 , pp. 508-522
    • Hogan, B.M.1    Hunter, M.P.2    Oates, A.C.3
  • 9
    • 4344689967 scopus 로고    scopus 로고
    • Zebrafish gcmb is required for pharyngeal cartilage formation
    • Hanaoka R, Ohmori Y, Uyemura K, et al. Zebrafish gcmb is required for pharyngeal cartilage formation. Mech Dev 2004; 121:1235-1247.
    • (2004) Mech Dev , vol.121 , pp. 1235-1247
    • Hanaoka, R.1    Ohmori, Y.2    Uyemura, K.3
  • 10
    • 0034772381 scopus 로고    scopus 로고
    • Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB
    • Ding C, Buckingham B, Levine MA. Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB. J Clin Invest 2001; 108:1215-1220.
    • (2001) J Clin Invest , vol.108 , pp. 1215-1220
    • Ding, C.1    Buckingham, B.2    Levine, M.A.3
  • 11
    • 19844366553 scopus 로고    scopus 로고
    • GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone
    • Thomee C, Schubert SW, Parma J, et al. GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone. J Clin Endocrinol Metab 2005; 90:2487-2492.
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 2487-2492
    • Thomee, C.1    Schubert, S.W.2    Parma, J.3
  • 12
    • 42049115231 scopus 로고    scopus 로고
    • Analysis of the GCM2 gene in isolated hypoparathyroidism: A molecular and biochemical study
    • Maret A, Ding C, Kornfield SL, Levine MA. Analysis of the GCM2 gene in isolated hypoparathyroidism: a molecular and biochemical study. J Clin Endocrinol Metab 2008; 93:1426-1432.
    • (2008) J Clin Endocrinol Metab , vol.93 , pp. 1426-1432
    • Maret, A.1    Ding, C.2    Kornfield, S.L.3    Levine, M.A.4
  • 13
    • 10644230307 scopus 로고    scopus 로고
    • GCMB gene, a master regulator of parathyroid gland development, expression, and regulation in hyperparathyroidism
    • Kebebew E, Peng M, Wong MG, et al. GCMB gene, a master regulator of parathyroid gland development, expression, and regulation in hyperparathyroidism. Surgery 2004; 136:1261-1266.
    • (2004) Surgery , vol.136 , pp. 1261-1266
    • Kebebew, E.1    Peng, M.2    Wong, M.G.3
  • 14
    • 0029153727 scopus 로고
    • Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1
    • Neubuser A, Koseki H, Balling R. Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1. Dev Biol 1995; 170:701-716.
    • (1995) Dev Biol , vol.170 , pp. 701-716
    • Neubuser, A.1    Koseki, H.2    Balling, R.3
  • 15
    • 0032169255 scopus 로고    scopus 로고
    • Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities
    • Peters H, Neubuser A, Kratochwil K, Balling R. Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev 1998; 12:2735-2747.
    • (1998) Genes Dev , vol.12 , pp. 2735-2747
    • Peters, H.1    Neubuser, A.2    Kratochwil, K.3    Balling, R.4
  • 16
    • 0035881214 scopus 로고    scopus 로고
    • Hoxa3 and pax1 regulate epithelial cell death and proliferation during thymus and parathyroid organogenesis
    • Su D, Ellis S, Napier A, et al. Hoxa3 and pax1 regulate epithelial cell death and proliferation during thymus and parathyroid organogenesis. Dev Biol 2001; 236:316-329.
    • (2001) Dev Biol , vol.236 , pp. 316-329
    • Su, D.1    Ellis, S.2    Napier, A.3
  • 17
    • 33646185393 scopus 로고    scopus 로고
    • Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1
    • Zou D, Silvius D, Davenport J, et al. Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1. Dev Biol 2006; 293:499-512.
    • (2006) Dev Biol , vol.293 , pp. 499-512
    • Zou, D.1    Silvius, D.2    Davenport, J.3
  • 18
    • 0029030722 scopus 로고
    • The role of Hoxa-3 in mouse thymus and thyroid development
    • Manley NR, Capecchi MR. The role of Hoxa-3 in mouse thymus and thyroid development. Development 1995; 121:1989-2003.
    • (1995) Development , vol.121 , pp. 1989-2003
    • Manley, N.R.1    Capecchi, M.R.2
  • 19
    • 2442642680 scopus 로고    scopus 로고
    • The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse
    • Kameda Y, Arai Y, Nishimaki T, Chisaka O. The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse. J HistochemCytochem 2004; 52:641-651.
    • (2004) J HistochemCytochem , vol.52 , pp. 641-651
    • Kameda, Y.1    Arai, Y.2    Nishimaki, T.3    Chisaka, O.4
  • 20
    • 0031887992 scopus 로고    scopus 로고
    • Zebrafish hox genes: Genomic organization and modified colinear expression patterns in the trunk
    • Prince VE, Joly L, Ekker M, Ho RK. Zebrafish hox genes: genomic organization and modified colinear expression patterns in the trunk. Development 1998; 125:407-420.
    • (1998) Development , vol.125 , pp. 407-420
    • Prince, V.E.1    Joly, L.2    Ekker, M.3    Ho, R.K.4
  • 21
    • 25844503071 scopus 로고    scopus 로고
    • Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1
    • Ivins S, Lammerts van Beuren K, Roberts C, et al. Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. Dev Biol 2005; 285:554-569.
    • (2005) Dev Biol , vol.285 , pp. 554-569
    • Ivins, S.1    Lammerts van Beuren, K.2    Roberts, C.3
  • 22
    • 0142149329 scopus 로고    scopus 로고
    • The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans
    • Piotrowski T, Ahn DG, Schilling TF, et al. The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans. Development 2003; 130:5043-5052.
    • (2003) Development , vol.130 , pp. 5043-5052
    • Piotrowski, T.1    Ahn, D.G.2    Schilling, T.F.3
  • 23
    • 0034721115 scopus 로고    scopus 로고
    • GATA3 haplo-insufficiency causes human HDR syndrome
    • Van Esch H, Groenen P, Nesbit MA, et al. GATA3 haplo-insufficiency causes human HDR syndrome. Nature 2000; 406:419-422.
    • (2000) Nature , vol.406 , pp. 419-422
    • Van Esch, H.1    Groenen, P.2    Nesbit, M.A.3
  • 24
    • 0029087975 scopus 로고
    • Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis
    • Pandolfi PP, Roth ME, Karis A, et al. Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis. Nat Genet 1995; 11:40-44.
    • (1995) Nat Genet , vol.11 , pp. 40-44
    • Pandolfi, P.P.1    Roth, M.E.2    Karis, A.3
  • 25
    • 0029014815 scopus 로고
    • Expression of zebrafish GATA 3 (gta3) during gastrulation and neurulation suggests a role in the specification of cell fate
    • Neave B, Rodaway A, Wilson SW, et al. Expression of zebrafish GATA 3 (gta3) during gastrulation and neurulation suggests a role in the specification of cell fate. Mech Dev 1995; 51:169-182.
    • (1995) Mech Dev , vol.51 , pp. 169-182
    • Neave, B.1    Rodaway, A.2    Wilson, S.W.3
  • 26
    • 26444453686 scopus 로고    scopus 로고
    • An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism
    • Bowl MR, Nesbit MA, Harding B, et al. An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism. J Clin Invest 2005; 115:2822-2831.
    • (2005) J Clin Invest , vol.115 , pp. 2822-2831
    • Bowl, M.R.1    Nesbit, M.A.2    Harding, B.3
  • 27
    • 33644902045 scopus 로고    scopus 로고
    • Comparative genomic and expression analysis of group B1 sox genes in zebrafish indicates their diversification during vertebrate evolution
    • Okuda Y, Yoda H, Uchikawa M, et al. Comparative genomic and expression analysis of group B1 sox genes in zebrafish indicates their diversification during vertebrate evolution. Dev Dyn 2006; 235:811-825.
    • (2006) Dev Dyn , vol.235 , pp. 811-825
    • Okuda, Y.1    Yoda, H.2    Uchikawa, M.3
  • 28
    • 0032842838 scopus 로고    scopus 로고
    • Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
    • Xu PX, Adams J, Peters H, et al. Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat Genet 1999; 23:113-117.
    • (1999) Nat Genet , vol.23 , pp. 113-117
    • Xu, P.X.1    Adams, J.2    Peters, H.3
  • 29
    • 0036333792 scopus 로고    scopus 로고
    • Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid
    • Xu PX, Zheng W, Laclef C, et al. Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid. Development 2002; 129:3033-3044.
    • (2002) Development , vol.129 , pp. 3033-3044
    • Xu, P.X.1    Zheng, W.2    Laclef, C.3
  • 30
    • 10344262883 scopus 로고    scopus 로고
    • Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes
    • Zou D, Silvius D, Fritzsch B, Xu PX. Eya1 and Six1 are essential for early steps of sensory neurogenesis in mammalian cranial placodes. Development 2004; 131:5561-5572.
    • (2004) Development , vol.131 , pp. 5561-5572
    • Zou, D.1    Silvius, D.2    Fritzsch, B.3    Xu, P.X.4
  • 31
    • 0036800398 scopus 로고    scopus 로고
    • An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome
    • Frank DU, Fotheringham LK, Brewer JA, et al. An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome. Development 2002; 129:4591-4603.
    • (2002) Development , vol.129 , pp. 4591-4603
    • Frank, D.U.1    Fotheringham, L.K.2    Brewer, J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.