Clinical, pathological, and molecular studies of two families with lodide organification defect-Reference-Cited by-同舟云学术

Clinical, pathological, and molecular studies of two families with lodide organification defect

Published:1997-03 Issue:1 Volume:8 Page:37-47
ISSN:1046-3976
Container-title:Endocrine Pathology
language:en
Short-container-title:Endocr Pathol

Author:

Rego Katia G. M.,Billerbeck Ana Elisa C.,Targovnik Hector M.,Santos Cecília L. S.,Alkmin Maria G.,Barbosa Sonia,Camargo Rosalinda,Medeiros-Neto Geraldo

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF02739706.pdf

Reference28 articles.

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2. Kimura S, Hong Y-S, Kotani T, Ohtaki S, Kikkawa F. Structure of the human thyroid peroxidase gene: comparison and relationship to the human myeloperoxidase gene. Biochemistry 28:4481–4489, 1989.

3. de Vijlder JJM, Dinsart C, Libert F, van Kessel AG, Bikker H, Bolhuis PA, Vassart G. Regional localization of the gene for thyroid peroxidase to human chromosome 2pter-p12. Cytogenet Cell Genet 47:170–172, 1988.

4. Barnett PS, Jones TA, McGregor AM, Banga JP, Sheer D. Regional sublocalization of the human peroxidase gene (TPO) by tritium and fluorescence in situ hybridization to chromosome 2p25→p24. Cytogenet Cell Genet 62:188,189, 1993.

5. Kimura S, Kotani T, McBride OW, Umeki K, Hirai K, Nakayama T, Ohtaki S. Human thyroid peroxidase: complete cDNA and protein sequence, chromosome mapping and identification of two alternatively spliced mRNAs. Proc Nat Acad Sci USA 84:5555–5559, 1987.

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