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Items: 1 to 20 of 44

1.

Specific ablation of mouse Fam20C in cells expressing type I collagen leads to skeletal defects and hypophosphatemia.

Liu P, Ma S, Zhang H, Liu C, Lu Y, Chen L, Qin C.

Sci Rep. 2017 Jun 15;7(1):3590. doi: 10.1038/s41598-017-03960-x.

2.

Structure of Fam20A reveals a pseudokinase featuring a unique disulfide pattern and inverted ATP-binding.

Cui J, Zhu Q, Zhang H, Cianfrocco MA, Leschziner AE, Dixon JE, Xiao J.

Elife. 2017 Apr 22;6. pii: e23990. doi: 10.7554/eLife.23990.

3.

Heritable and acquired disorders of phosphate metabolism: Etiologies involving FGF23 and current therapeutics.

Clinkenbeard EL, White KE.

Bone. 2017 Jan 31. pii: S8756-3282(17)30034-0. doi: 10.1016/j.bone.2017.01.034. [Epub ahead of print]

PMID:
28159712
4.

Canine models of human rare disorders.

Hytönen MK, Lohi H.

Rare Dis. 2016 Sep 28;4(1):e1241362. eCollection 2016.

5.

How rare bone diseases have informed our knowledge of complex diseases.

Johnson ML.

Bonekey Rep. 2016 Sep 21;5:839. doi: 10.1038/bonekey.2016.69. eCollection 2016. Review.

PMID:
27688878
6.

Vertebrate Lonesome Kinase Regulated Extracellular Matrix Protein Phosphorylation, Cell Shape, and Adhesion in Trabecular Meshwork Cells.

Maddala R, Skiba NP, Rao PV.

J Cell Physiol. 2017 Sep;232(9):2447-2460. doi: 10.1002/jcp.25582. Epub 2017 Mar 27.

PMID:
27591737
7.

FAM20A binds to and regulates FAM20C localization.

Ohyama Y, Lin JH, Govitvattana N, Lin IP, Venkitapathi S, Alamoudi A, Husein D, An C, Hotta H, Kaku M, Mochida Y.

Sci Rep. 2016 Jun 13;6:27784. doi: 10.1038/srep27784.

8.

Loss of epithelial FAM20A in mice causes amelogenesis imperfecta, tooth eruption delay and gingival overgrowth.

Li LL, Liu PH, Xie XH, Ma S, Liu C, Chen L, Qin CL.

Int J Oral Sci. 2016 Jun 30;8(2):98-109. doi: 10.1038/ijos.2016.14.

9.

Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.

Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H.

PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May.

10.

Phosphorylation of spore coat proteins by a family of atypical protein kinases.

Nguyen KB, Sreelatha A, Durrant ES, Lopez-Garrido J, Muszewska A, Dudkiewicz M, Grynberg M, Yee S, Pogliano K, Tomchick DR, Pawłowski K, Dixon JE, Tagliabracci VS.

Proc Natl Acad Sci U S A. 2016 Jun 21;113(25):E3482-91. doi: 10.1073/pnas.1605917113. Epub 2016 May 16.

11.

A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing.

Poulter JA, Smith CE, Murrillo G, Silva S, Feather S, Howell M, Crinnion L, Bonthron DT, Carr IM, Watson CM, Inglehearn CF, Mighell AJ.

Mol Genet Genomic Med. 2015 Oct 4;3(6):543-9. doi: 10.1002/mgg3.164. eCollection 2015 Nov.

12.

Dentin Matrix Proteins in Bone Tissue Engineering.

Ravindran S, George A.

Adv Exp Med Biol. 2015;881:129-42. doi: 10.1007/978-3-319-22345-2_8. Review.

13.

Family with sequence similarity member 20C is the primary but not the only kinase for the small-integrin-binding ligand N-linked glycoproteins in bone.

Yang X, Yan W, Tian Y, Ma P, Opperman LA, Wang X.

FASEB J. 2016 Jan;30(1):121-8. doi: 10.1096/fj.15-273607. Epub 2015 Aug 31.

14.

High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes.

Brommage R, Liu J, Hansen GM, Kirkpatrick LL, Potter DG, Sands AT, Zambrowicz B, Powell DR, Vogel P.

Bone Res. 2014 Oct 28;2:14034. doi: 10.1038/boneres.2014.34. eCollection 2014.

15.

A Single Kinase Generates the Majority of the Secreted Phosphoproteome.

Tagliabracci VS, Wiley SE, Guo X, Kinch LN, Durrant E, Wen J, Xiao J, Cui J, Nguyen KB, Engel JL, Coon JJ, Grishin N, Pinna LA, Pagliarini DJ, Dixon JE.

Cell. 2015 Jun 18;161(7):1619-32. doi: 10.1016/j.cell.2015.05.028.

16.

What is the point of pseudokinases?

Raju S, Shaw AS.

Elife. 2015 May 6;4:e07771. doi: 10.7554/eLife.07771.

17.

Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations.

Acevedo AC, Poulter JA, Alves PG, de Lima CL, Castro LC, Yamaguti PM, Paula LM, Parry DA, Logan CV, Smith CE, Johnson CA, Inglehearn CF, Mighell AJ.

BMC Med Genet. 2015 Feb 21;16:8. doi: 10.1186/s12881-015-0154-5.

18.

The secretory pathway kinases.

Sreelatha A, Kinch LN, Tagliabracci VS.

Biochim Biophys Acta. 2015 Oct;1854(10 Pt B):1687-93. doi: 10.1016/j.bbapap.2015.03.015. Epub 2015 Apr 8. Review.

19.

Immortalized Mouse Floxed Fam20c Dental Papillar Mesenchymal and Osteoblast Cell Lines Retain Their Primary Characteristics.

Liu C, Wang X, Zhang H, Xie X, Liu P, Liu Y, Jani PH, Lu Y, Chen S, Qin C.

J Cell Physiol. 2015 Nov;230(11):2581-7. doi: 10.1002/jcp.25008.

20.

Phosphorylation and Alternative Splicing of 7B2 Reduce Prohormone Convertase 2 Activation.

Ramos-Molina B, Lindberg I.

Mol Endocrinol. 2015 May;29(5):756-64. doi: 10.1210/me.2014-1394. Epub 2015 Mar 26.

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