PubMed (GeneRIF) for id: 79083

Year	Number of Results
2002	5
2003	1
2004	1
2006	1
2011	1
2012	1
2014	1
2015	1
2016	2
2017	1
2019	2
2020	2
2024	0

1

RAB27A/Melanophilin Blocker Inhibits Melanoma Cell Motility and Invasion.

Guo D, Jain R, Hwang JS, Weninger W, Beaumont KA, Tikoo S. Guo D, et al. J Invest Dermatol. 2020 Jul;140(7):1470-1473.e3. doi: 10.1016/j.jid.2019.12.023. Epub 2020 Jan 22. J Invest Dermatol. 2020. PMID: 31978414 Free article. No abstract available.

2

Single-nucleotide polymorphism rs13426236 contributes to an increased prostate cancer risk via regulating MLPH splicing variant 4.

Xiao F, Zhang P, Wang Y, Tian Y, James M, Huang CC, Wang L, Wang L. Xiao F, et al. Mol Carcinog. 2020 Jan;59(1):45-55. doi: 10.1002/mc.23127. Epub 2019 Oct 29. Mol Carcinog. 2020. PMID: 31659808 Free PMC article.

3

Fusion of ALK to the melanophilin gene MLPH in pediatric Spitz nevi.

Chung CT, Marrano P, Swanson D, Dickson BC, Thorner PS. Chung CT, et al. Hum Pathol. 2019 May;87:57-64. doi: 10.1016/j.humpath.2019.03.002. Epub 2019 Mar 8. Hum Pathol. 2019. PMID: 30857967

4

Genetic 3'UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight.

Hernando B, Peña-Chilet M, Ibarrola-Villava M, Martin-Gonzalez M, Gomez-Fernandez C, Ribas G, Martinez-Cadenas C. Hernando B, et al. Exp Dermatol. 2017 Oct;26(10):896-903. doi: 10.1111/exd.13333. Epub 2017 May 9. Exp Dermatol. 2017. PMID: 28266728

5

A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism.

Netter P, Chan SK, Banerjee PP, Monaco-Shawver L, Noroski LM, Hanson IC, Forbes LR, Mace EM, Chinen J, Gaspar HB, Sleiman P, Hakonarson H, Klein C, Ehlayel MS, Orange JS. Netter P, et al. J Allergy Clin Immunol. 2016 Aug;138(2):599-601.e3. doi: 10.1016/j.jaci.2015.12.1337. Epub 2016 Mar 23. J Allergy Clin Immunol. 2016. PMID: 27016801 Free PMC article. No abstract available.

6

Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites.

Bu H, Narisu N, Schlick B, Rainer J, Manke T, Schäfer G, Pasqualini L, Chines P, Schweiger MR, Fuchsberger C, Klocker H. Bu H, et al. Hum Mutat. 2016 Jan;37(1):52-64. doi: 10.1002/humu.22909. Epub 2015 Oct 19. Hum Mutat. 2016. PMID: 26411452 Free PMC article.

7

The GTPase-deficient Rab27A(Q78L) mutant inhibits melanosome transport in melanocytes through trapping of Rab27A effector protein Slac2-a/melanophilin in their cytosol: development of a novel melanosome-targetinG tag.

Ishida M, Arai SP, Ohbayashi N, Fukuda M. Ishida M, et al. J Biol Chem. 2014 Apr 18;289(16):11059-11067. doi: 10.1074/jbc.M114.552281. Epub 2014 Feb 28. J Biol Chem. 2014. PMID: 24584932 Free PMC article.

8

Cellular and clinical report of new Griscelli syndrome type III cases.

Westbroek W, Klar A, Cullinane AR, Ziegler SG, Hurvitz H, Ganem A, Wilson K, Dorward H, Huizing M, Tamimi H, Vainshtein I, Berkun Y, Lavie M, Gahl WA, Anikster Y. Westbroek W, et al. Pigment Cell Melanoma Res. 2012 Jan;25(1):47-56. doi: 10.1111/j.1755-148X.2011.00901.x. Epub 2011 Oct 3. Pigment Cell Melanoma Res. 2012. PMID: 21883982 Free PMC article.

9

High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts.

Park JW, Cai J, McIntosh I, Jabs EW, Fallin MD, Ingersoll R, Hetmanski JB, Vekemans M, Attie-Bitach T, Lovett M, Scott AF, Beaty TH. Park JW, et al. J Med Genet. 2006 Jul;43(7):598-608. doi: 10.1136/jmg.2005.040162. Epub 2006 Jan 13. J Med Genet. 2006. PMID: 16415175 Free PMC article.

10

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.

Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K. Lukusa T, et al. Genet Couns. 2004;15(3):293-301. Genet Couns. 2004. PMID: 15517821

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