PubMed for id: 5500

Year	Number of Results
1994	2
1995	1
1996	1
1997	1
1998	1
1999	2
2000	4
2001	5
2002	8
2003	3
2004	7
2005	8
2006	3
2007	6
2008	3
2009	4
2010	10
2011	17
2012	14
2013	14
2014	12
2015	23
2016	17
2017	16
2018	15
2019	17
2020	18
2021	20
2022	21
2023	13
2024	2

1

The expression and clinical prognostic value of protein phosphatase 1 catalytic subunit beta in pancreatic cancer.

Hu L, Xu H, Wang X, Wu B, Chen F, Chen W, Gao Y, Zhong Z. Hu L, et al. Bioengineered. 2021 Dec;12(1):2763-2778. doi: 10.1080/21655979.2021.1934243. Bioengineered. 2021. PMID: 34125004 Free PMC article.

2

Noonan syndrome with loose anagen hair with variants in the PPP1CB gene: First familial case reported.

Huckstadt V, Chinton J, Gomez A, Obregon MG, Gravina LP. Huckstadt V, et al. Am J Med Genet A. 2021 Apr;185(4):1256-1260. doi: 10.1002/ajmg.a.62089. Epub 2021 Jan 25. Am J Med Genet A. 2021. PMID: 33491856

3

A case report of Noonan syndrome-like disorder with loose anagen hair 2 treated with recombinant human growth hormone.

Zhou P, Zhu L, Fan Q, Liu Y, Zhang T, Yang T, Chen J, Cheng Q, Li T, Chen L. Zhou P, et al. Am J Med Genet A. 2020 Aug;182(8):1967-1971. doi: 10.1002/ajmg.a.61638. Epub 2020 Jun 1. Am J Med Genet A. 2020. PMID: 32476286

4

Integrative genomics analysis of eQTL and GWAS summary data identifies PPP1CB as a novel bone mineral density risk genes.

Zhai Y, Yu L, Shao Y, Wang J. Zhai Y, et al. Biosci Rep. 2020 Apr 30;40(4):BSR20193185. doi: 10.1042/BSR20193185. Biosci Rep. 2020. PMID: 32266926 Free PMC article.

5

The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual: Broadening the clinical phenotype.

Bertola D, Yamamoto G, Buscarilli M, Jorge A, Passos-Bueno MR, Kim C. Bertola D, et al. Am J Med Genet A. 2017 Mar;173(3):824-828. doi: 10.1002/ajmg.a.38070. Am J Med Genet A. 2017. PMID: 28211982 Review.

6

De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease.

Ma L, Bayram Y, McLaughlin HM, Cho MT, Krokosky A, Turner CE, Lindstrom K, Bupp CP, Mayberry K, Mu W, Bodurtha J, Weinstein V, Zadeh N, Alcaraz W, Powis Z, Shao Y, Scott DA, Lewis AM, White JJ, Jhangiani SN, Gulec EY, Lalani SR, Lupski JR, Retterer K, Schnur RE, Wentzensen IM, Bale S, Chung WK. Ma L, et al. Hum Genet. 2016 Dec;135(12):1399-1409. doi: 10.1007/s00439-016-1731-1. Epub 2016 Sep 28. Hum Genet. 2016. PMID: 27681385 Free PMC article.

7

A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair.

Gripp KW, Aldinger KA, Bennett JT, Baker L, Tusi J, Powell-Hamilton N, Stabley D, Sol-Church K, Timms AE, Dobyns WB. Gripp KW, et al. Am J Med Genet A. 2016 Sep;170(9):2237-47. doi: 10.1002/ajmg.a.37781. Epub 2016 Jun 5. Am J Med Genet A. 2016. PMID: 27264673 Free PMC article.

8

Protein Phosphatase 1 Beta is Modulated by Chronic Hypoxia and Involved in the Angiogenic Endothelial Cell Migration.

Iacobazzi D, Garaeva I, Albertario A, Cherif M, Angelini GD, Caputo M, Ghorbel MT. Iacobazzi D, et al. Cell Physiol Biochem. 2015;36(1):384-94. doi: 10.1159/000430257. Epub 2015 May 7. Cell Physiol Biochem. 2015. PMID: 25967976 Free article.

9

Protein phosphatase-1 inhibitor-3 is co-localized to the nucleoli and centrosomes with PP1gamma1 and PP1alpha, respectively.

Huang HS, Pozarowski P, Gao Y, Darzynkiewicz Z, Lee EY. Huang HS, et al. Arch Biochem Biophys. 2005 Nov 15;443(1-2):33-44. doi: 10.1016/j.abb.2005.08.021. Arch Biochem Biophys. 2005. PMID: 16256067

10

Characterization of the protein phosphatase 1 catalytic subunit in endothelium: involvement in contractile responses.

Verin AD, Csortos C, Durbin SD, Aydanyan A, Wang P, Patterson CE, Garcia JG. Verin AD, et al. J Cell Biochem. 2000 Jul 19;79(1):113-25. J Cell Biochem. 2000. PMID: 10906760

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