PubMed (OMIM) for id: 897127

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Year	Number of Results
1995	1
1996	2
1999	1
2002	2
2023	0

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Page 1

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.

Hocking LJ, Lucas GJ, Daroszewska A, Mangion J, Olavesen M, Cundy T, Nicholson GC, Ward L, Bennett ST, Wuyts W, Van Hul W, Ralston SH. Hocking LJ, et al. Hum Mol Genet. 2002 Oct 15;11(22):2735-9. doi: 10.1093/hmg/11.22.2735. Hum Mol Genet. 2002. PMID: 12374763

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone.

Laurin N, Brown JP, Morissette J, Raymond V. Laurin N, et al. Am J Hum Genet. 2002 Jun;70(6):1582-8. doi: 10.1086/340731. Epub 2002 Apr 30. Am J Hum Genet. 2002. PMID: 11992264 Free PMC article.

Differential stimulation of PKC phosphorylation of potassium channels by ZIP1 and ZIP2.

Gong J, Xu J, Bezanilla M, van Huizen R, Derin R, Li M. Gong J, et al. Science. 1999 Sep 3;285(5433):1565-9. doi: 10.1126/science.285.5433.1565. Science. 1999. PMID: 10477520

p62, a phosphotyrosine-independent ligand of the SH2 domain of p56lck, belongs to a new class of ubiquitin-binding proteins.

Vadlamudi RK, Joung I, Strominger JL, Shin J. Vadlamudi RK, et al. J Biol Chem. 1996 Aug 23;271(34):20235-7. doi: 10.1074/jbc.271.34.20235. J Biol Chem. 1996. PMID: 8702753 Free article.

Molecular cloning of a phosphotyrosine-independent ligand of the p56lck SH2 domain.

Joung I, Strominger JL, Shin J. Joung I, et al. Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5991-5. doi: 10.1073/pnas.93.12.5991. Proc Natl Acad Sci U S A. 1996. PMID: 8650207 Free PMC article.

Phosphotyrosine-independent binding of a 62-kDa protein to the src homology 2 (SH2) domain of p56lck and its regulation by phosphorylation of Ser-59 in the lck unique N-terminal region.

Park I, Chung J, Walsh CT, Yun Y, Strominger JL, Shin J. Park I, et al. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12338-42. doi: 10.1073/pnas.92.26.12338. Proc Natl Acad Sci U S A. 1995. PMID: 8618896 Free PMC article.

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