SCOPUS 정보 검색 플랫폼

Journal of Clinical Endocrinology and Metabolism

Volumn 84, Issue 7, 1999, Pages 2574-2576

Sulfate transport is not impaired in pendred syndrome thyrocytes

(7) Kraiem, Z a,b Heinrich, R a Sadeh, O a Shiloni, E a,b Nassir, E c Hazani, E c Glaser, Benjamin d,e

a CARMEL MEDICAL CENTER (Israel)

b TECHNION ISRAEL INSTITUTE OF TECHNOLOGY (Israel)

c Nahariya Hospital Israel (Israel)

d HEBREW UNIVERSITY (Israel)

e HADASSAH HEBREW UNIVERSITY MEDICAL CENTER (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; IODIDE; PENDRIN; SULFATE; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CONTROLLED STUDY; GENE FUNCTION; GOITER; HUMAN; HUMAN CELL; ION TRANSPORT; PENDRED SYNDROME; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROTEIN ANALYSIS; THYROID CELL;

EID: 0033306085 PISSN: 0021972X EISSN: None Source Type: Journal
DOI: 10.1210/jcem.84.7.5973 Document Type: Article

Times cited : (30)

References (12)

1
- 0001385507
- Deaf mutism and goitre
- (1896) Lancet , vol.2 , pp. 523
- Pendred, V.¹

2
- 0000570814
- Deafness with sporadic goiter: Pendred syndrome
- (1962) Arch Otolaryng , vol.76 , pp. 401-406
- Batsakis, J.G.¹ Nishiyama, R.H.²

3
- 0028086199
- Clinical and molecular genetics studies in Pendred's syndrome
- (1994) Thyroid , vol.4 , pp. 279-284
- Billerbeck, A.E.C.¹ Cavaliere, H.² Goldberg, A.C.³ Kalil, J.⁴ Medeiros-Neto, G.⁵

4
- 0029963073
- Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification
- (1996) Nat Genet , vol.12 , pp. 424-426
- Sheffield, V.C.¹ Kraiem, Z.² Beck, J.C.³ Nishimura, D.⁴ Stone, E.M.⁵ Salameh, M.⁶ Sadeh, O.⁷ Glaser, B.⁸

5
- 16944366606
- Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
- (1997) Nat Genet , vol.17 , pp. 411-422
- Everett, L.A.¹ Glaser, B.² Beck, J.C.³ Idol, J.R.⁴ Buchs, A.⁵ Heyman, M.⁶ Adawi, F.⁷ Hazani, E.⁸ Nassir, E.⁹ Baxevanis, A.D.¹⁰ Sheffield, V.C.¹¹ Green, E.D.¹²

6
- 0031565089
- Sounds from the cochlea
- (1997) Nature , vol.390 , pp. 559-560
- Avraham, K.B.¹

7
- 0008290326
- A new type of gene associated with hereditary deafness?
- (1998) Mol. Med. Today , vol.4 , pp. 52
- Coffey, A.¹

8
- 0031810527
- Surprising news: A putative sulfate transporter is defective in Pendred's syndrome
- (1998) Eur J Endocrinol , vol.138 , pp. 623-624
- Rutishauser, J.¹ Kopp, P.²

9
- 0030698825
- Sounding out a novel sulphate transporter
- (1997) Nat Genet , vol.17 , pp. 370
- Morton, C.C.¹

10
- 0008289877
- The Pendred syndrome (PDS) gene product functions as an iodide, chloride transporter
- In Press
- (1999) Nat Genet
- Scott, D.A.¹ Wang, R.² Kerman, T.M.³ Sheffield, V.C.⁴ Karniski, L.P.⁵

11
- 0025789657
- Iodide uptake and organification, tri-iodothyronine secretion, cyclic AMP accumulation and cell proliferation in an optimized system of human thyroid follicles cultured in collagen gel suspended in serum-free medium
- (1991) J Endocrinol , vol.131 , pp. 499-506
- Kraiem, Z.¹ Sadeh, O.² Yosef, M.³

12
- 0028898547
- Mutual antagonistic interactions between the thyrotropin (adenosine 3',5'-monophosphate) and protein kinase C/epidermal growth factor (tyrosine kinase) pathways in cell proliferation and differentiation of cultured human thyroid follicles
- (1995) Endocrinology , vol.136 , pp. 585-590
- Kraiem, Z.¹ Sadeh, O.² Yosef, M.³ Aharon, A.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.