Citations for
1CSNK1A1, FAM83H
The conserved C-terminal residues of FAM83H are required for the recruitment of casein kinase 1 to the keratin cytoskeleton
Kuga T, Inoue N, Sometani K, Murataka S, Saraya M, Sugita R, Mikami T, Takeda Y, Taniguchi M, Nishida K, Yamagishi N.
Sci Rep. Jul 12;12(1):11819. doi: 10.1038/s41598-022-16153-y. 2022
2FAM83H, TRIM29
TRIM29 in Cutaneous Squamous Cell Carcinoma
Hsu CY, Yanagi T, Ujiie H.
Front Med (Lausanne). Dec 20;8:804166. doi: 10.3389/fmed.2021.804166. 2021
3AIH4, FAM83H
FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta.
Wang SK, Zhang H, Hu CY, Liu JF, Chadha S, Kim JW, Simmer JP, Hu JCC.
J Dent Res. Mar;100(3):293-301. doi: 10.1177/0022034520962731. Epub 2020 Oct 9. 2021
4FAM83H
The Enamel Phenotype in Homozygous Fam83h Truncation Mice.
Wang SK, Hu Y, Smith CE, Yang J, Zeng C, Kim JW, Hu JC, Simmer JP.
Mol Genet Genomic Med. Jun;7(6):e724. doi: 10.1002/mgg3.724. Epub 2019 May 6. 2019
5AIH4, FAM83H
Fam83h mutation inhibits the mineralization in ameloblasts by activating Wnt/β-catenin signaling pathway.
Yang M, Huang W, Yang F, Zhang T, Wang C, Song Y.
Biochem Biophys Res Commun. Jun 18;501(1):206-211. doi: 10.1016/j.bbrc.2018.04.216. Epub 2018 May 3. 2018
6FAM83H
FAM83H is involved in the progression of hepatocellular carcinoma and is regulated by MYC
Kim KM, Park SH, Bae JS, Noh SJ, Tao GZ, Kim JR, Kwon KS, Park HS, Park BH, Lee H, Chung MJ, Moon WS, Sylvester KG, Jang KY.
Sci Rep. Jun 12;7(1):3274. doi: 10.1038/s41598-017-03639-3. 2017
7FAM83H
Evolutionary analysis of FAM83H in vertebrates
Huang W, Yang M, Wang C, Song Y.
PLoS One. Jul 6;12(7):e0180360. doi: 10.1371/journal.pone.0180360. 2017
8AIH4, CSNK1A1, FAM83H
FAM83H and casein kinase I regulate the organization of the keratin cytoskeleton and formation of desmosomes
Kuga T, Sasaki M, Mikami T, Miake Y, Adachi J, Shimizu M, Saito Y, Koura M, Takeda Y, Matsuda J, Tomonaga T, Nakayama Y.
Sci Rep. May 25;6:26557. doi: 10.1038/srep26557. 2016
9AIH4, FAM83H
Fam83h null mice support a neomorphic mechanism for human ADHCAI
Wang SK, Hu Y, Yang J, Smith CE, Richardson AS, Yamakoshi Y, Lee YL, Seymen F, Koruyucu M, Gencay K, Lee M, Choi M, Kim JW, Hu JC, Simmer JP.
Mol Genet Genomic Med. Sep 21;4(1):46-67. doi: 10.1002/mgg3.178. 2015
10CSNK1A1, FAM83H
A novel mechanism of keratin cytoskeleton organization through casein kinase Iα and FAM83H in colorectal cancer.
Kuga T, Kume H, Kawasaki N, Sato M, Adachi J, Shiromizu T, Hoshino I, Nishimori T, Matsubara H, Tomonaga T.
J Cell Sci. Oct 15;126(Pt 20):4721-31. doi: 10.1242/jcs.129684. Epub 2013 Jul 31. 2013
11FAM83H, SEDO
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
Hart PS, Becerik S, Cogulu D, Emingil G, Ozdemir-Ozenen D, Han ST, Sulima PP, Firatli E, Hart TC.
Clin Genet 75(4):401-4. Epub 2009 Feb 11. No abstract available. 2009
12FAM83H, AIH4
FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta.
Kim JW, Lee SK, Lee ZH, Park JC, Lee KE, Lee MH, Park JT, Seo BM, Hu JC, Simmer JP.
Am J Hum Genet 82(2):489-94. 2008