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Journal Abstract Search

210 related items for PubMed ID: 22556420

  • 21. The structural basis for the collagen processing by human P3H1/CRTAP/PPIB ternary complex.
    Li W, Peng J, Yao D, Rao B, Xia Y, Wang Q, Li S, Cao M, Shen Y, Ma P, Liao R, Qin A, Zhao J, Cao Y.
    Nat Commun; 2024 Sep 08; 15(1):7844. PubMed ID: 39245686
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  • 23. 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 15; 19(2):223-34. PubMed ID: 19846465
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  • 24. Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix.
    Barnes AM, Cabral WA, Weis M, Makareeva E, Mertz EL, Leikin S, Eyre D, Trujillo C, Marini JC.
    Hum Mutat; 2012 Nov 15; 33(11):1589-98. PubMed ID: 22718341
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  • 26. 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 15; 76(19):3899-3914. PubMed ID: 30993352
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  • 27. Ziploc-ing the structure 2.0: Endoplasmic reticulum-resident peptidyl prolyl isomerases show different activities toward hydroxyproline.
    Ishikawa Y, Mizuno K, Bächinger HP.
    J Biol Chem; 2017 Jun 02; 292(22):9273-9282. PubMed ID: 28385890
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  • 28. Vascular Ehlers-Danlos syndrome mutations in type III collagen differently stall the triple helical folding.
    Mizuno K, Boudko S, Engel J, Bächinger HP.
    J Biol Chem; 2013 Jun 28; 288(26):19166-76. PubMed ID: 23645670
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  • 29. High level expression and characterization of the cyclophilin B gene from the anaerobic fungus Orpinomyces sp. strain PC-2.
    Chen H, Li XL, Xu H, Ljungdahl LG, Cerniglia CE.
    Protein Pept Lett; 2006 Jun 28; 13(7):727-32. PubMed ID: 17018017
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  • 30. Depletion of cyclophilins B and C leads to dysregulation of endoplasmic reticulum redox homeostasis.
    Stocki P, Chapman DC, Beach LA, Williams DB.
    J Biol Chem; 2014 Aug 15; 289(33):23086-23096. PubMed ID: 24990953
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  • 31. Tensile properties in collagen-rich tissues of Quarter Horses with hereditary equine regional dermal asthenia (HERDA).
    Bowser JE, Elder SH, Pasquali M, Grady JG, Rashmir-Raven AM, Wills R, Swiderski CE.
    Equine Vet J; 2014 Mar 15; 46(2):216-22. PubMed ID: 23738970
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  • 32. Cyclophilin B Deficiency Causes Abnormal Dentin Collagen Matrix.
    Terajima M, Taga Y, Cabral WA, Nagasawa M, Sumida N, Hattori S, Marini JC, Yamauchi M.
    J Proteome Res; 2017 Aug 04; 16(8):2914-2923. PubMed ID: 28696707
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  • 33. Inorganic polyphosphate controls cyclophilin B-mediated collagen folding in osteoblast-like cells.
    Khong ML, Li L, Solesio ME, Pavlov EV, Tanner JA.
    FEBS J; 2020 Oct 04; 287(20):4500-4524. PubMed ID: 32056376
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  • 34. Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta.
    Marini JC, Cabral WA, Barnes AM.
    Cell Tissue Res; 2010 Jan 04; 339(1):59-70. PubMed ID: 19862557
    [Abstract] [Full Text] [Related]

  • 35. Identification of Salmonella Typhimurium Peptidyl-prolyl cis-trans Isomerase B (PPIase B) and Assessment of their Role in the Protein Folding.
    Kumawat M, Karuna I, Ahlawat N, Ahlawat S.
    Protein Pept Lett; 2020 Jan 04; 27(8):744-750. PubMed ID: 32096737
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  • 37. Cyclophilin-promoted folding of mouse dihydrofolate reductase does not include the slow conversion of the late-folding intermediate to the active enzyme.
    von Ahsen O, Lim JH, Caspers P, Martin F, Schönfeld HJ, Rassow J, Pfanner N.
    J Mol Biol; 2000 Mar 31; 297(3):809-18. PubMed ID: 10731431
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