230 related articles for article (PubMed ID: 18487197)
1. Characterization of recombinant human prolyl 3-hydroxylase isoenzyme 2, an enzyme modifying the basement membrane collagen IV.
Tiainen P; Pasanen A; Sormunen R; Myllyharju J
J Biol Chem; 2008 Jul; 283(28):19432-9. PubMed ID: 18487197
[TBL] [Abstract][Full Text] [Related]
2. Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations.
Hudson DM; Joeng KS; Werther R; Rajagopal A; Weis M; Lee BH; Eyre DR
J Biol Chem; 2015 Mar; 290(13):8613-22. PubMed ID: 25645914
[TBL] [Abstract][Full Text] [Related]
3. Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta.
Marini JC; Cabral WA; Barnes AM
Cell Tissue Res; 2010 Jan; 339(1):59-70. PubMed ID: 19862557
[TBL] [Abstract][Full Text] [Related]
4. Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex.
Chang W; Barnes AM; Cabral WA; Bodurtha JN; Marini JC
Hum Mol Genet; 2010 Jan; 19(2):223-34. PubMed ID: 19846465
[TBL] [Abstract][Full Text] [Related]
5. Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix.
Valli M; Barnes AM; Gallanti A; Cabral WA; Viglio S; Weis MA; Makareeva E; Eyre D; Leikin S; Antoniazzi F; Marini JC; Mottes M
Clin Genet; 2012 Nov; 82(5):453-9. PubMed ID: 21955071
[TBL] [Abstract][Full Text] [Related]
6. Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues.
Homan EP; Lietman C; Grafe I; Lennington J; Morello R; Napierala D; Jiang MM; Munivez EM; Dawson B; Bertin TK; Chen Y; Lua R; Lichtarge O; Hicks J; Weis MA; Eyre D; Lee BH
PLoS Genet; 2014 Jan; 10(1):e1004121. PubMed ID: 24465224
[TBL] [Abstract][Full Text] [Related]
7. Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone development.
Marini JC; Cabral WA; Barnes AM; Chang W
Cell Cycle; 2007 Jul; 6(14):1675-81. PubMed ID: 17630507
[TBL] [Abstract][Full Text] [Related]
8. Collagen prolyl 3-hydroxylation: a major role for a minor post-translational modification?
Hudson DM; Eyre DR
Connect Tissue Res; 2013; 54(4-5):245-51. PubMed ID: 23772978
[TBL] [Abstract][Full Text] [Related]
9. An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1·cartilage-associated protein·cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.
Ishikawa Y; Bächinger HP
J Biol Chem; 2013 Nov; 288(44):31437-46. PubMed ID: 24043621
[TBL] [Abstract][Full Text] [Related]
10. Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation.
Willaert A; Malfait F; Symoens S; Gevaert K; Kayserili H; Megarbane A; Mortier G; Leroy JG; Coucke PJ; De Paepe A
J Med Genet; 2009 Apr; 46(4):233-41. PubMed ID: 19088120
[TBL] [Abstract][Full Text] [Related]
11. Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes.
Pyott SM; Schwarze U; Christiansen HE; Pepin MG; Leistritz DF; Dineen R; Harris C; Burton BK; Angle B; Kim K; Sussman MD; Weis M; Eyre DR; Russell DW; McCarthy KJ; Steiner RD; Byers PH
Hum Mol Genet; 2011 Apr; 20(8):1595-609. PubMed ID: 21282188
[TBL] [Abstract][Full Text] [Related]
12. Severe osteogenesis imperfecta in cyclophilin B-deficient mice.
Choi JW; Sutor SL; Lindquist L; Evans GL; Madden BJ; Bergen HR; Hefferan TE; Yaszemski MJ; Bram RJ
PLoS Genet; 2009 Dec; 5(12):e1000750. PubMed ID: 19997487
[TBL] [Abstract][Full Text] [Related]
13. Collagen prolyl 4-hydroxylase isoenzymes I and II have sequence specificity towards different X-Pro-Gly triplets.
Salo AM; Rappu P; Koski MK; Karjalainen E; Izzi V; Drushinin K; Miinalainen I; Käpylä J; Heino J; Myllyharju J
Matrix Biol; 2024 Jan; 125():73-87. PubMed ID: 38081527
[TBL] [Abstract][Full Text] [Related]
14. Biological role of prolyl 3-hydroxylation in type IV collagen.
Pokidysheva E; Boudko S; Vranka J; Zientek K; Maddox K; Moser M; Fässler R; Ware J; Bächinger HP
Proc Natl Acad Sci U S A; 2014 Jan; 111(1):161-6. PubMed ID: 24368846
[TBL] [Abstract][Full Text] [Related]
15. Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype.
Tonelli F; Cotti S; Leoni L; Besio R; Gioia R; Marchese L; Giorgetti S; Villani S; Gistelinck C; Wagener R; Kobbe B; Fiedler IAK; Larionova D; Busse B; Eyre D; Rossi A; Witten PE; Forlino A
Matrix Biol; 2020 Aug; 90():40-60. PubMed ID: 32173581
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive
Zhytnik L; Duy BH; Eekhoff M; Wisse L; Pals G; Reimann E; Kõks S; Märtson A; Maugeri A; Maasalu K; Micha D
Genes (Basel); 2022 Feb; 13(3):. PubMed ID: 35327962
[TBL] [Abstract][Full Text] [Related]
17. CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.
Baldridge D; Schwarze U; Morello R; Lennington J; Bertin TK; Pace JM; Pepin MG; Weis M; Eyre DR; Walsh J; Lambert D; Green A; Robinson H; Michelson M; Houge G; Lindman C; Martin J; Ward J; Lemyre E; Mitchell JJ; Krakow D; Rimoin DL; Cohn DH; Byers PH; Lee B
Hum Mutat; 2008 Dec; 29(12):1435-42. PubMed ID: 18566967
[TBL] [Abstract][Full Text] [Related]
18. Characterization of PPIB interaction in the P3H1 ternary complex and implications for its pathological mutations.
Wu J; Zhang W; Xia L; Feng L; Shu Z; Zhang J; Ye W; Zeng N; Zhou A
Cell Mol Life Sci; 2019 Oct; 76(19):3899-3914. PubMed ID: 30993352
[TBL] [Abstract][Full Text] [Related]
19. Prolyl 3-hydroxylase 1, enzyme characterization and identification of a novel family of enzymes.
Vranka JA; Sakai LY; Bächinger HP
J Biol Chem; 2004 May; 279(22):23615-21. PubMed ID: 15044469
[TBL] [Abstract][Full Text] [Related]
20. Characterization of a second Arabidopsis thaliana prolyl 4-hydroxylase with distinct substrate specificity.
Tiainen P; Myllyharju J; Koivunen P
J Biol Chem; 2005 Jan; 280(2):1142-8. PubMed ID: 15528200
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
