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Items: 12

1.

A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis.

Johnson MR, Polymeropoulos MH, Vos HL, Ortiz de Luna RI, Francomano CA.

Genome Res. 1996 Nov;6(11):1050-5.

2.

Pycnodysostosis: role and regulation of cathepsin K in osteoclast function and human disease.

Motyckova G, Fisher DE.

Curr Mol Med. 2002 Aug;2(5):407-21. Review.

PMID:
12125807
3.

Cathepsin K and the design of inhibitors of cathepsin K.

Yamashita DS, Dodds RA.

Curr Pharm Des. 2000 Jan;6(1):1-24. Review.

PMID:
10637370
4.

The role of cathepsin K in normal bone resorption.

Troen BR.

Drug News Perspect. 2004 Jan-Feb;17(1):19-28. Review.

PMID:
14993931
5.

[Pycnodysostosis--common ancestor of some Danish patients. Examination and diagnosis based on molecular genetics].

Haagerup A, Christensen MF, Hertz JM, Kruse TA.

Ugeskr Laeger. 2002 Feb 11;164(7):887-90. Review. Danish.

PMID:
11881551
6.

Decreased bone turnover and deterioration of bone structure in two cases of pycnodysostosis.

Fratzl-Zelman N, Valenta A, Roschger P, Nader A, Gelb BD, Fratzl P, Klaushofer K.

J Clin Endocrinol Metab. 2004 Apr;89(4):1538-47. Review.

PMID:
15070910
7.

Clinical and animal research findings in pycnodysostosis and gene mutations of cathepsin K from 1996 to 2011.

Xue Y, Cai T, Shi S, Wang W, Zhang Y, Mao T, Duan X.

Orphanet J Rare Dis. 2011 May 10;6:20. doi: 10.1186/1750-1172-6-20. Review.

8.

Current molecular techniques and strategies for gene localization.

Verma A, Maheshwari MC.

J Assoc Physicians India. 1992 Jun;40(6):405-8. Review. No abstract available.

PMID:
1452568
9.

Cathepsin K: a unique collagenolytic cysteine peptidase.

Novinec M, Lenarčič B.

Biol Chem. 2013 Sep;394(9):1163-79. doi: 10.1515/hsz-2013-0134. Review.

PMID:
23629523
10.

The role of cathepsin K in oral and maxillofacial disorders.

Wen X, Yi LZ, Liu F, Wei JH, Xue Y.

Oral Dis. 2016 Mar;22(2):109-15. doi: 10.1111/odi.12378. Epub 2015 Nov 23. Review.

PMID:
26458004
11.

Molecular genetics and ocular disease.

Wiggs JL.

Int Ophthalmol Clin. 1993 Spring;33(2):1-36. Review. No abstract available.

PMID:
8325725
12.

Inherited diseases caused by mutations in cathepsin protease genes.

Ketterer S, Gomez-Auli A, Hillebrand LE, Petrera A, Ketscher A, Reinheckel T.

FEBS J. 2017 May;284(10):1437-1454. doi: 10.1111/febs.13980. Epub 2017 Jan 12. Review.

PMID:
27926992

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