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Items: 6

1.

INK4 locus of the tumor-resistant rodent, the naked mole rat, expresses a functional p15/p16 hybrid isoform.

Tian X, Azpurua J, Ke Z, Augereau A, Zhang ZD, Vijg J, Gladyshev VN, Gorbunova V, Seluanov A.

Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):1053-8. doi: 10.1073/pnas.1418203112. Epub 2014 Dec 30.

2.

Electrostatic interactions mediate binding of obscurin to small ankyrin 1: biochemical and molecular modeling studies.

Busby B, Oashi T, Willis CD, Ackermann MA, Kontrogianni-Konstantopoulos A, Mackerell AD Jr, Bloch RJ.

J Mol Biol. 2011 Apr 29;408(2):321-34. doi: 10.1016/j.jmb.2011.01.053. Epub 2011 Feb 17.

3.

GRIM-19 and p16(INK4a) synergistically regulate cell cycle progression and E2F1-responsive gene expression.

Sun P, Nallar SC, Raha A, Kalakonda S, Velalar CN, Reddy SP, Kalvakolanu DV.

J Biol Chem. 2010 Sep 3;285(36):27545-52. doi: 10.1074/jbc.M110.105767. Epub 2010 Jun 3.

4.

Simulation of different truncated p16(INK4a) forms and in silico study of interaction with Cdk4.

Fahham N, Ghahremani MH, Sardari S, Vaziri B, Ostad SN.

Cancer Inform. 2009;7:1-11. Epub 2008 Dec 3.

5.

Selectivity and potency of cyclin-dependent kinase inhibitors.

Sridhar J, Akula N, Pattabiraman N.

AAPS J. 2006 Mar 24;8(1):E204-21. Review.

6.

Utilizing NMR to study the structure of growth-inhibitory proteins.

Marassi F.

Methods Mol Biol. 2003;223:3-15. Review. No abstract available.

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