Literature DB >> 9497262

A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.

S Yamamoto, M Okada, M Tsujikawa, Y Shimomura, K Nishida, Y Inoue, H Watanabe, N Maeda, H Kurahashi, S Kinoshita, Y Nakamura, Y Tano.   

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Year:  1998        PMID： 9497262      PMCID： PMC1376959          DOI： 10.1086/301765

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  21 in total

1.  Corneal amyloidosis caused by Leu518Pro mutation of betaig-h3 gene.

Authors:  K Hirano; Y Hotta; K Fujiki; A Kanai
Journal:  Br J Ophthalmol       Date:  2000-06       Impact factor: 4.638

2.  Homozygous mutation (L527R) of TGFBI in an individual with lattice corneal dystrophy.

Authors:  N Yamada; T-I Chikama; N Morishige; R Yanai; T Nishida; M Inui; K Seki
Journal:  Br J Ophthalmol       Date:  2005-06       Impact factor: 4.638

3.  A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.

Authors:  Ping Yu; Yangshun Gu; Yuehong Yang; Xiaoyi Yan; Lili Chen; Zhen Ge; Ming Qi; Jianmin Si; Lei Guo
Journal:  J Genet       Date:  2006-04       Impact factor: 1.166

4.  Keratoepithelin in secondary corneal amyloidosis.

Authors:  D Suesskind; C Auw-Haedrich; D F Schorderet; F L Munier; K U Loeffler
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2005-12-06       Impact factor: 3.117

5.  Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.

Authors:  H S Stewart; R Parveen; A E Ridgway; R Bonshek; G C Black
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

6.  H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people.

Authors:  H M Chau; N T Ha; L X Cung; T K Thanh; K Fujiki; A Murakami; A Kanai
Journal:  Br J Ophthalmol       Date:  2003-06       Impact factor: 4.638

7.  Purification, characterization and N-terminal sequences alignment of a mannose specific protein purified from Potca fish, Tetraodon patoca.

Authors:  Nurul Absar; Sohel Hasan; F Arisaka
Journal:  Protein J       Date:  2008-02       Impact factor: 2.371

8.  A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.

Authors:  Anthony J Aldave; Vivek S Yellore; Baris Sonmez; Nirit Bourla; Andrew K Salem; M Ali Khan; Sylvia A Rayner; Ben J Glasgow
Journal:  Arch Ophthalmol       Date:  2008-03

Review 9.  The IC3D classification of the corneal dystrophies.

Authors:  Jayne S Weiss; H U Møller; Walter Lisch; Shigeru Kinoshita; Anthony J Aldave; Michael W Belin; Tero Kivelä; Massimo Busin; Francis L Munier; Berthold Seitz; John Sutphin; Cecilie Bredrup; Mark J Mannis; Christopher J Rapuano; Gabriel Van Rij; Eung Kweon Kim; Gordon K Klintworth
Journal:  Cornea       Date:  2008-12       Impact factor: 2.651

10.  Denaturation and solvent effect on the conformation and fibril formation of TGFBIp.

Authors:  Heather L Grothe; Morgan R Little; Angela S Cho; Andrew J W Huang; Ching Yuan
Journal:  Mol Vis       Date:  2009-12-08       Impact factor: 2.367
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