[cite web | title = Entrez Gene: TGFBI transforming growth factor, beta-induced, 68kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7045| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
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*cite journal | author=Schmitt-Bernard CF, Pouliquen Y, Argilès A |title= [BIG-H3 protein: mutation of codon 124 and corneal amyloidosis] |journal=Journal français d'ophtalmologie |volume=27 |issue= 5 |pages= 510–22 |year= 2004 |pmid= 15179309 |doi=
*cite journal | author=Pieramici SF, Afshari NA |title=Genetics of corneal dystrophies: the evolving landscape. |journal=Current opinion in ophthalmology |volume=17 |issue= 4 |pages= 361–6 |year= 2006 |pmid= 16900028 |doi= 10.1097/01.icu.0000233955.94347.84
*cite journal | author=Skonier J, Neubauer M, Madisen L, "et al." |title=cDNA cloning and sequence analysis of beta ig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-beta. |journal=DNA Cell Biol. |volume=11 |issue= 7 |pages= 511–22 |year= 1992 |pmid= 1388724 |doi=
*cite journal | author=LeBaron RG, Bezverkov KI, Zimber MP, "et al." |title=Beta IG-H3, a novel secretory protein inducible by transforming growth factor-beta, is present in normal skin and promotes the adhesion and spreading of dermal fibroblasts in vitro. |journal=J. Invest. Dermatol. |volume=104 |issue= 5 |pages= 844–9 |year= 1995 |pmid= 7738366 |doi=
*cite journal | author=Skonier J, Bennett K, Rothwell V, "et al." |title=beta ig-h3: a transforming growth factor-beta-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice. |journal=DNA Cell Biol. |volume=13 |issue= 6 |pages= 571–84 |year= 1994 |pmid= 8024701 |doi=
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*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Stone EM, Mathers WD, Rosenwasser GO, "et al." |title=Three autosomal dominant corneal dystrophies map to chromosome 5q. |journal=Nat. Genet. |volume=6 |issue= 1 |pages= 47–51 |year= 1994 |pmid= 8136834 |doi= 10.1038/ng0194-47
*cite journal | author=Munier FL, Korvatska E, Djemaï A, "et al." |title=Kerato-epithelin mutations in four 5q31-linked corneal dystrophies. |journal=Nat. Genet. |volume=15 |issue= 3 |pages= 247–51 |year= 1997 |pmid= 9054935 |doi= 10.1038/ng0397-247
*cite journal | author=Hashimoto K, Noshiro M, Ohno S, "et al." |title=Characterization of a cartilage-derived 66-kDa protein (RGD-CAP/beta ig-h3) that binds to collagen. |journal=Biochim. Biophys. Acta |volume=1355 |issue= 3 |pages= 303–14 |year= 1997 |pmid= 9061001 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Korvatska E, Munier FL, Djemaï A, "et al." |title=Mutation hot spots in 5q31-linked corneal dystrophies. |journal=Am. J. Hum. Genet. |volume=62 |issue= 2 |pages= 320–4 |year= 1998 |pmid= 9463327 |doi=
*cite journal | author=Yamamoto S, Okada M, Tsujikawa M, "et al." |title=A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA. |journal=Am. J. Hum. Genet. |volume=62 |issue= 3 |pages= 719–22 |year= 1998 |pmid= 9497262 |doi=
*cite journal | author=Okada M, Yamamoto S, Watanabe H, "et al." |title=Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene. |journal=Am. J. Ophthalmol. |volume=126 |issue= 2 |pages= 169–76 |year= 1998 |pmid= 9727509 |doi=
*cite journal | author=Okada M, Yamamoto S, Tsujikawa M, "et al." |title=Two distinct kerato-epithelin mutations in Reis-Bücklers corneal dystrophy. |journal=Am. J. Ophthalmol. |volume=126 |issue= 4 |pages= 535–42 |year= 1998 |pmid= 9780098 |doi=
*cite journal | author=Fujiki K, Hotta Y, Nakayasu K, "et al." |title=A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities. |journal=Hum. Genet. |volume=103 |issue= 3 |pages= 286–9 |year= 1998 |pmid= 9799082 |doi=
*cite journal | author=Stewart H, Black GC, Donnai D, "et al." |title=A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy. |journal=Ophthalmology |volume=106 |issue= 5 |pages= 964–70 |year= 1999 |pmid= 10328397 |doi= 10.1016/S0161-6420(99)00539-4
*cite journal | author=Stewart HS, Ridgway AE, Dixon MJ, "et al." |title=Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis. |journal=Hum. Mutat. |volume=14 |issue= 2 |pages= 126–32 |year= 1999 |pmid= 10425035 |doi= 10.1002/(SICI)1098-1004(1999)14:2<126::AID-HUMU4>3.0.CO;2-W |doilabel=10.1002/(SICI)1098-1004(1999)14:2126::AID-HUMU43.0.CO;2-W
*cite journal | author=Rozzo C, Fossarello M, Galleri G, "et al." |title=A common beta ig-h3 gene mutation (delta f540) in a large cohort of Sardinian Reis Bücklers corneal dystrophy patients. Mutations in brief no. 180. Online. |journal=Hum. Mutat. |volume=12 |issue= 3 |pages= 215–6 |year= 2000 |pmid= 10660331 |doi=
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