277 related articles for article (PubMed ID: 25645914)
1. 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]
2. P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA.
Hudson DM; Weis M; Rai J; Joeng KS; Dimori M; Lee BH; Morello R; Eyre DR
J Biol Chem; 2017 Mar; 292(9):3877-3887. PubMed ID: 28115524
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Posttranslational modifications in type I collagen from different tissues extracted from wild type and prolyl 3-hydroxylase 1 null mice.
Pokidysheva E; Zientek KD; Ishikawa Y; Mizuno K; Vranka JA; Montgomery NT; Keene DR; Kawaguchi T; Okuyama K; Bächinger HP
J Biol Chem; 2013 Aug; 288(34):24742-52. PubMed ID: 23861401
[TBL] [Abstract][Full Text] [Related]
7. High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2.
Mordechai S; Gradstein L; Pasanen A; Ofir R; El Amour K; Levy J; Belfair N; Lifshitz T; Joshua S; Narkis G; Elbedour K; Myllyharju J; Birk OS
Am J Hum Genet; 2011 Sep; 89(3):438-45. PubMed ID: 21885030
[TBL] [Abstract][Full Text] [Related]
8. Type I and type V procollagen triple helix uses different subsets of the molecular ensemble for lysine posttranslational modifications in the rER.
Ishikawa Y; Taga Y; Zientek K; Mizuno N; Salo AM; Semenova O; Tufa SF; Keene DR; Holden P; Mizuno K; Gould DB; Myllyharju J; Bächinger HP
J Biol Chem; 2021; 296():100453. PubMed ID: 33631195
[TBL] [Abstract][Full Text] [Related]
9. A role for prolyl 3-hydroxylase 2 in post-translational modification of fibril-forming collagens.
Fernandes RJ; Farnand AW; Traeger GR; Weis MA; Eyre DR
J Biol Chem; 2011 Sep; 286(35):30662-30669. PubMed ID: 21757687
[TBL] [Abstract][Full Text] [Related]
10. Prolyl 3-Hydroxylase 2 Is a Molecular Player of Angiogenesis.
Pignata P; Apicella I; Cicatiello V; Puglisi C; Magliacane Trotta S; Sanges R; Tarallo V; De Falco S
Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33918807
[TBL] [Abstract][Full Text] [Related]
11. Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract.
Guo H; Tong P; Peng Y; Wang T; Liu Y; Chen J; Li Y; Tian Q; Hu Y; Zheng Y; Xiao L; Xiong W; Pan Q; Hu Z; Xia K
Clin Genet; 2014 Dec; 86(6):575-9. PubMed ID: 24172257
[TBL] [Abstract][Full Text] [Related]
12. Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones.
Vranka JA; Pokidysheva E; Hayashi L; Zientek K; Mizuno K; Ishikawa Y; Maddox K; Tufa S; Keene DR; Klein R; Bächinger HP
J Biol Chem; 2010 May; 285(22):17253-62. PubMed ID: 20363744
[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. Developmental Stage-dependent Regulation of Prolyl 3-Hydroxylation in Tendon Type I Collagen.
Taga Y; Kusubata M; Ogawa-Goto K; Hattori S
J Biol Chem; 2016 Jan; 291(2):837-47. PubMed ID: 26567337
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Role of prolyl hydroxylation in the molecular interactions of collagens.
Rappu P; Salo AM; Myllyharju J; Heino J
Essays Biochem; 2019 Sep; 63(3):325-335. PubMed ID: 31350381
[TBL] [Abstract][Full Text] [Related]
18. Distinct post-translational features of type I collagen are conserved in mouse and human periodontal ligament.
Hudson DM; Garibov M; Dixon DR; Popowics T; Eyre DR
J Periodontal Res; 2017 Dec; 52(6):1042-1049. PubMed ID: 28631261
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Hydroxylation of recombinant human collagen type I alpha 1 in transgenic maize co-expressed with a recombinant human prolyl 4-hydroxylase.
Xu X; Gan Q; Clough RC; Pappu KM; Howard JA; Baez JA; Wang K
BMC Biotechnol; 2011 Jun; 11():69. PubMed ID: 21702901
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
