"Structure and expression in breast tumors of human TIMP-3, a new member of the metalloproteinase inhibitor family."
Uria J.A. , Ferrando A.A. , Velasco G. , Freije J.M. , Lopez-Otin C.
Cancer Res.54:2091-2094(1994) [PubMed] [Europe PMC] [Abstract]

"Cloning and characterization of human tissue inhibitor of metalloproteinases-3."
Wilde C.G. , Hawkins P.R. , Coleman R.T. , Levine W.B. , Delegeane A.M. , Okamoto P.M. , Ito L.Y. , Scott R.W. , Seilhamer J.J.
DNA Cell Biol.13:711-718(1994) [PubMed] [Europe PMC] [Abstract]

"Cloning of cDNAs encoding human TIMP-3, a novel member of the tissue inhibitor of metalloproteinase family."
Silbiger S.M. , Jacobsen V.L. , Cupples R.L. , Koski R.A.
Gene141:293-297(1994) [PubMed] [Europe PMC] [Abstract]

"A novel member of human tissue inhibitor of metalloproteinases (TIMP) gene family is regulated during G1 progression, mitogenic stimulation, differentiation, and senescence."
Wick M. , Buerger C. , Bruesselbach S. , Lucibello F. , Mueller R.
J. Biol. Chem.269:18953-18960(1994) [PubMed] [Europe PMC] [Abstract]

"Genomic organization of the human tissue inhibitor of metalloproteinases-3 (TIMP3)."
Stoehr H. , Roomp K. , Felbor U. , Weber B.H.F.
Genome Res.5:483-487(1995) [PubMed] [Europe PMC] [Abstract]

"TIMP-3 is expressed in the human retinal pigment epithelium."
Ruiz A.C. , Brett P. , Bok D.
Biochem. Biophys. Res. Commun.226:467-474(1996) [PubMed] [Europe PMC] [Abstract]

"A genome annotation-driven approach to cloning the human ORFeome."
Collins J.E. , Wright C.L. , Edwards C.A. , Davis M.P. , Grinham J.A. , Cole C.G. , Goward M.E. , Aguado B. , Mallya M. , Mokrab Y. , Huckle E.J. , Beare D.M. , Dunham I.
Genome Biol.5:R84.1-R84.11(2004) [PubMed] [Europe PMC] [Abstract]

"Cloning of human full-length CDSs in BD Creator(TM) system donor vector."
Kalnine N. , Chen X. , Rolfs A. , Halleck A. , Hines L. , Eisenstein S. , Koundinya M. , Raphael J. , Moreira D. , Kelley T. , LaBaer J. , Lin Y. , Phelan M. , Farmer A.
Submitted (2003-05) to the EMBL/GenBank/DDBJ databases

"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T. , Suzuki Y. , Nishikawa T. , Otsuki T. , Sugiyama T. , Irie R. , Wakamatsu A. , Hayashi K. , Sato H. , Nagai K. , Kimura K. , Makita H. , Sekine M. , Obayashi M. , Nishi T. , Shibahara T. , Tanaka T. , Ishii S. , Yamamoto J. , Saito K. , Kawai Y. , Isono Y. , Nakamura Y. , Nagahari K. , Murakami K. , Yasuda T. , Iwayanagi T. , Wagatsuma M. , Shiratori A. , Sudo H. , Hosoiri T. , Kaku Y. , Kodaira H. , Kondo H. , Sugawara M. , Takahashi M. , Kanda K. , Yokoi T. , Furuya T. , Kikkawa E. , Omura Y. , Abe K. , Kamihara K. , Katsuta N. , Sato K. , Tanikawa M. , Yamazaki M. , Ninomiya K. , Ishibashi T. , Yamashita H. , Murakawa K. , Fujimori K. , Tanai H. , Kimata M. , Watanabe M. , Hiraoka S. , Chiba Y. , Ishida S. , Ono Y. , Takiguchi S. , Watanabe S. , Yosida M. , Hotuta T. , Kusano J. , Kanehori K. , Takahashi-Fujii A. , Hara H. , Tanase T.-O. , Nomura Y. , Togiya S. , Komai F. , Hara R. , Takeuchi K. , Arita M. , Imose N. , Musashino K. , Yuuki H. , Oshima A. , Sasaki N. , Aotsuka S. , Yoshikawa Y. , Matsunawa H. , Ichihara T. , Shiohata N. , Sano S. , Moriya S. , Momiyama H. , Satoh N. , Takami S. , Terashima Y. , Suzuki O. , Nakagawa S. , Senoh A. , Mizoguchi H. , Goto Y. , Shimizu F. , Wakebe H. , Hishigaki H. , Watanabe T. , Sugiyama A. , Takemoto M. , Kawakami B. , Yamazaki M. , Watanabe K. , Kumagai A. , Itakura S. , Fukuzumi Y. , Fujimori Y. , Komiyama M. , Tashiro H. , Tanigami A. , Fujiwara T. , Ono T. , Yamada K. , Fujii Y. , Ozaki K. , Hirao M. , Ohmori Y. , Kawabata A. , Hikiji T. , Kobatake N. , Inagaki H. , Ikema Y. , Okamoto S. , Okitani R. , Kawakami T. , Noguchi S. , Itoh T. , Shigeta K. , Senba T. , Matsumura K. , Nakajima Y. , Mizuno T. , Morinaga M. , Sasaki M. , Togashi T. , Oyama M. , Hata H. , Watanabe M. , Komatsu T. , Mizushima-Sugano J. , Satoh T. , Shirai Y. , Takahashi Y. , Nakagawa K. , Okumura K. , Nagase T. , Nomura N. , Kikuchi H. , Masuho Y. , Yamashita R. , Nakai K. , Yada T. , Nakamura Y. , Ohara O. , Isogai T. , Sugano S. more...
Nat. Genet.36:40-45(2004) [PubMed] [Europe PMC] [Abstract]

"The DNA sequence of human chromosome 22."
Dunham I. , Hunt A.R. , Collins J.E. , Bruskiewich R. , Beare D.M. , Clamp M. , Smink L.J. , Ainscough R. , Almeida J.P. , Babbage A.K. , Bagguley C. , Bailey J. , Barlow K.F. , Bates K.N. , Beasley O.P. , Bird C.P. , Blakey S.E. , Bridgeman A.M. , Buck D. , Burgess J. , Burrill W.D. , Burton J. , Carder C. , Carter N.P. , Chen Y. , Clark G. , Clegg S.M. , Cobley V.E. , Cole C.G. , Collier R.E. , Connor R. , Conroy D. , Corby N.R. , Coville G.J. , Cox A.V. , Davis J. , Dawson E. , Dhami P.D. , Dockree C. , Dodsworth S.J. , Durbin R.M. , Ellington A.G. , Evans K.L. , Fey J.M. , Fleming K. , French L. , Garner A.A. , Gilbert J.G.R. , Goward M.E. , Grafham D.V. , Griffiths M.N.D. , Hall C. , Hall R.E. , Hall-Tamlyn G. , Heathcott R.W. , Ho S. , Holmes S. , Hunt S.E. , Jones M.C. , Kershaw J. , Kimberley A.M. , King A. , Laird G.K. , Langford C.F. , Leversha M.A. , Lloyd C. , Lloyd D.M. , Martyn I.D. , Mashreghi-Mohammadi M. , Matthews L.H. , Mccann O.T. , Mcclay J. , Mclaren S. , McMurray A.A. , Milne S.A. , Mortimore B.J. , Odell C.N. , Pavitt R. , Pearce A.V. , Pearson D. , Phillimore B.J.C.T. , Phillips S.H. , Plumb R.W. , Ramsay H. , Ramsey Y. , Rogers L. , Ross M.T. , Scott C.E. , Sehra H.K. , Skuce C.D. , Smalley S. , Smith M.L. , Soderlund C. , Spragon L. , Steward C.A. , Sulston J.E. , Swann R.M. , Vaudin M. , Wall M. , Wallis J.M. , Whiteley M.N. , Willey D.L. , Williams L. , Williams S.A. , Williamson H. , Wilmer T.E. , Wilming L. , Wright C.L. , Hubbard T. , Bentley D.R. , Beck S. , Rogers J. , Shimizu N. , Minoshima S. , Kawasaki K. , Sasaki T. , Asakawa S. , Kudoh J. , Shintani A. , Shibuya K. , Yoshizaki Y. , Aoki N. , Mitsuyama S. , Roe B.A. , Chen F. , Chu L. , Crabtree J. , Deschamps S. , Do A. , Do T. , Dorman A. , Fang F. , Fu Y. , Hu P. , Hua A. , Kenton S. , Lai H. , Lao H.I. , Lewis J. , Lewis S. , Lin S.-P. , Loh P. , Malaj E. , Nguyen T. , Pan H. , Phan S. , Qi S. , Qian Y. , Ray L. , Ren Q. , Shaull S. , Sloan D. , Song L. , Wang Q. , Wang Y. , Wang Z. , White J. , Willingham D. , Wu H. , Yao Z. , Zhan M. , Zhang G. , Chissoe S. , Murray J. , Miller N. , Minx P. , Fulton R. , Johnson D. , Bemis G. , Bentley D. , Bradshaw H. , Bourne S. , Cordes M. , Du Z. , Fulton L. , Goela D. , Graves T. , Hawkins J. , Hinds K. , Kemp K. , Latreille P. , Layman D. , Ozersky P. , Rohlfing T. , Scheet P. , Walker C. , Wamsley A. , Wohldmann P. , Pepin K. , Nelson J. , Korf I. , Bedell J.A. , Hillier L.W. , Mardis E. , Waterston R. , Wilson R. , Emanuel B.S. , Shaikh T. , Kurahashi H. , Saitta S. , Budarf M.L. , McDermid H.E. , Johnson A. , Wong A.C.C. , Morrow B.E. , Edelmann L. , Kim U.J. , Shizuya H. , Simon M.I. , Dumanski J.P. , Peyrard M. , Kedra D. , Seroussi E. , Fransson I. , Tapia I. , Bruder C.E. , O'Brien K.P. , Wilkinson P. , Bodenteich A. , Hartman K. , Hu X. , Khan A.S. , Lane L. , Tilahun Y. , Wright H. more...
Nature402:489-495(1999) [PubMed] [Europe PMC] [Abstract]

Mural R.J. , Istrail S. , Sutton G.G. , Florea L. , Halpern A.L. , Mobarry C.M. , Lippert R. , Walenz B. , Shatkay H. , Dew I. , Miller J.R. , Flanigan M.J. , Edwards N.J. , Bolanos R. , Fasulo D. , Halldorsson B.V. , Hannenhalli S. , Turner R. , Yooseph S. , Lu F. , Nusskern D.R. , Shue B.C. , Zheng X.H. , Zhong F. , Delcher A.L. , Huson D.H. , Kravitz S.A. , Mouchard L. , Reinert K. , Remington K.A. , Clark A.G. , Waterman M.S. , Eichler E.E. , Adams M.D. , Hunkapiller M.W. , Myers E.W. , Venter J.C. more...
Submitted (2005-07) to the EMBL/GenBank/DDBJ databases

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

"Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP3 gene to chromosome 22."
Apte S.S. , Mattei M.-G. , Olsen B.R.
Genomics19:86-90(1994) [PubMed] [Europe PMC] [Abstract]

"Identification and characterization of human tissue inhibitor of metalloproteinase-3 and detection of three additional metalloproteinase inhibitor activities in extracellular matrix."
Kishnani N.S. , Staskus P.W. , Yang T.-T. , Masiarz F.R. , Hawkes S.P.
Matrix Biol.14:479-488(1995) [PubMed] [Europe PMC] [Abstract]

"Cloning and partial structure of the gene encoding human tissue inhibitor of metalloproteinases-3."
Hammani K. , Henriet P.M. , Silbiger S.M. , DeClerck Y.A.
Gene170:287-288(1996) [PubMed] [Europe PMC] [Abstract]

"Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a binding partner of epithelial growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1). Implications for macular degenerations."
Klenotic P.A. , Munier F.L. , Marmorstein L.Y. , Anand-Apte B.
J. Biol. Chem.279:30469-30473(2004) [PubMed] [Europe PMC] [Abstract]

"Structural determinants of the ADAM inhibition by TIMP-3: crystal structure of the TACE-N-TIMP-3 complex."
Wisniewska M. , Goettig P. , Maskos K. , Belouski E. , Winters D. , Hecht R. , Black R. , Bode W.
J. Mol. Biol.381:1307-1319(2008) [PubMed] [Europe PMC] [Abstract]

"Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy."
Weber B.H.F. , Vogt G. , Pruett R.C. , Stoehr H. , Felbor U.
Nat. Genet.8:352-356(1994) [PubMed] [Europe PMC] [Abstract]

"A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical features."
Felbor U. , Stoehr H. , Amann T. , Schoenherr U. , Weber B.H.F.
Hum. Mol. Genet.4:2415-2416(1995) [PubMed] [Europe PMC] [Abstract]

"Night blindness in Sorsby's fundus dystrophy reversed by vitamin A."
Jacobson S.G. , Cideciyan A.V. , Regunath G. , Rodriguez F.J. , Vandenburgh K. , Sheffield V.C. , Stone E.M.
Nat. Genet.11:27-32(1995) [PubMed] [Europe PMC] [Abstract]

"A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy."
Felbor U. , Stoehr H. , Amann T. , Schoenherr U. , Apfelstedt-Sylla E. , Weber B.H.F.
J. Med. Genet.33:233-236(1996) [PubMed] [Europe PMC] [Abstract]

"Autosomal recessive Sorsby fundus dystrophy revisited: molecular evidence for dominant inheritance."
Felbor U. , Suvanto E.A. , Forsius H.R. , Eriksson A.W. , Weber B.H.
Am. J. Hum. Genet.60:57-62(1997) [PubMed] [Europe PMC] [Abstract]