R37CA49152/CA/NCI NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
2005	2
2006	1
2007	3
2008	1
2009	2
2011	2
2012	3
2013	3
2022	0

1

Methods to monitor classical protein-tyrosine phosphatase oxidation.

Karisch R, Neel BG. Karisch R, et al. FEBS J. 2013 Jan;280(2):459-75. doi: 10.1111/j.1742-4658.2012.08626.x. Epub 2012 May 30. FEBS J. 2013. PMID: 22577968 Free PMC article. Review.

2

Global proteomic assessment of the classical protein-tyrosine phosphatome and "Redoxome".

Karisch R, Fernandez M, Taylor P, Virtanen C, St-Germain JR, Jin LL, Harris IS, Mori J, Mak TW, Senis YA, Östman A, Moran MF, Neel BG. Karisch R, et al. Cell. 2011 Sep 2;146(5):826-40. doi: 10.1016/j.cell.2011.07.020. Cell. 2011. PMID: 21884940 Free PMC article.

3

Germline gain-of-function mutations in SOS1 cause Noonan syndrome.

Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Kucherlapati RS. Roberts AE, et al. Nat Genet. 2007 Jan;39(1):70-4. doi: 10.1038/ng1926. Epub 2006 Dec 3. Nat Genet. 2007. PMID: 17143285

4

Distinct roles for neutrophils and dendritic cells in inflammation and autoimmunity in motheaten mice.

Abram CL, Roberge GL, Pao LI, Neel BG, Lowell CA. Abram CL, et al. Immunity. 2013 Mar 21;38(3):489-501. doi: 10.1016/j.immuni.2013.02.018. Immunity. 2013. PMID: 23521885 Free PMC article.

5

Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signalling.

Yang W, Wang J, Moore DC, Liang H, Dooner M, Wu Q, Terek R, Chen Q, Ehrlich MG, Quesenberry PJ, Neel BG. Yang W, et al. Nature. 2013 Jul 25;499(7459):491-5. doi: 10.1038/nature12396. Epub 2013 Jul 17. Nature. 2013. PMID: 23863940 Free PMC article.

6

Increased BRAF heterodimerization is the common pathogenic mechanism for noonan syndrome-associated RAF1 mutants.

Wu X, Yin J, Simpson J, Kim KH, Gu S, Hong JH, Bayliss P, Backx PH, Neel BG, Araki T. Wu X, et al. Mol Cell Biol. 2012 Oct;32(19):3872-90. doi: 10.1128/MCB.00751-12. Epub 2012 Jul 23. Mol Cell Biol. 2012. PMID: 22826437 Free PMC article.

7

Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia.

Kratz CP, Niemeyer CM, Thomas C, Bauhuber S, Matejas V, Bergsträsser E, Flotho C, Flores NJ, Haas O, Hasle H, van den Heuvel-Eibrink MM, Kucherlapati RS, Lang P, Roberts AE, Starý J, Strahm B, Swanson KD, Trebo M, Zecca M, Neel B, Locatelli F, Loh ML, Zenker M. Kratz CP, et al. Leukemia. 2007 May;21(5):1108-9. doi: 10.1038/sj.leu.2404620. Epub 2007 Feb 22. Leukemia. 2007. PMID: 17315019 No abstract available.

8

Control of CNS cell-fate decisions by SHP-2 and its dysregulation in Noonan syndrome.

Gauthier AS, Furstoss O, Araki T, Chan R, Neel BG, Kaplan DR, Miller FD. Gauthier AS, et al. Neuron. 2007 Apr 19;54(2):245-62. doi: 10.1016/j.neuron.2007.03.027. Neuron. 2007. PMID: 17442246 Free PMC article.

9

Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes.

Keilhack H, David FS, McGregor M, Cantley LC, Neel BG. Keilhack H, et al. J Biol Chem. 2005 Sep 2;280(35):30984-93. doi: 10.1074/jbc.M504699200. Epub 2005 Jun 29. J Biol Chem. 2005. PMID: 15987685 Free article.

10

SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients.

Swanson KD, Winter JM, Reis M, Bentires-Alj M, Greulich H, Grewal R, Hruban RH, Yeo CJ, Yassin Y, Iartchouk O, Montgomery K, Whitman SP, Caligiuri MA, Loh ML, Gilliland DG, Look AT, Kucherlapati R, Kern SE, Meyerson M, Neel BG. Swanson KD, et al. Genes Chromosomes Cancer. 2008 Mar;47(3):253-9. doi: 10.1002/gcc.20527. Genes Chromosomes Cancer. 2008. PMID: 18064648

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