These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 27803445)

  • 21. New molecular components supporting ryanodine receptor-mediated Ca(2+) release: roles of junctophilin and TRIC channel in embryonic cardiomyocytes.
    Yamazaki D; Yamazaki T; Takeshima H
    Pharmacol Ther; 2009 Mar; 121(3):265-72. PubMed ID: 19095005
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Essential role of the TRIC-B channel in Ca2+ handling of alveolar epithelial cells and in perinatal lung maturation.
    Yamazaki D; Komazaki S; Nakanishi H; Mishima A; Nishi M; Yazawa M; Yamazaki T; Taguchi R; Takeshima H
    Development; 2009 Jul; 136(14):2355-61. PubMed ID: 19515693
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pore architecture of TRIC channels and insights into their gating mechanism.
    Yang H; Hu M; Guo J; Ou X; Cai T; Liu Z
    Nature; 2016 Oct; 538(7626):537-541. PubMed ID: 27698420
    [TBL] [Abstract][Full Text] [Related]  

  • 24. TRIC-A regulates intracellular Ca
    Zhou X; Li A; Lin PH; Zhou J; Ma J
    Pflugers Arch; 2021 Mar; 473(3):547-556. PubMed ID: 33474637
    [TBL] [Abstract][Full Text] [Related]  

  • 25. IFITM5 mutations and osteogenesis imperfecta.
    Hanagata N
    J Bone Miner Metab; 2016 Mar; 34(2):123-31. PubMed ID: 26031935
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Classification of Osteogenesis Imperfecta revisited.
    Van Dijk FS; Pals G; Van Rijn RR; Nikkels PG; Cobben JM
    Eur J Med Genet; 2010; 53(1):1-5. PubMed ID: 19878741
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The biophysical properties of TRIC-A and TRIC-B and their interactions with RyR2.
    Hu J; Venturi E; Sigalas C; Murayama T; Nishi M; Takeshima H; Sitsapesan R
    J Gen Physiol; 2023 Nov; 155(11):. PubMed ID: 37756589
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutations in patients with osteogenesis imperfecta from consanguineous Indian families.
    Stephen J; Girisha KM; Dalal A; Shukla A; Shah H; Srivastava P; Kornak U; Phadke SR
    Eur J Med Genet; 2015 Jan; 58(1):21-7. PubMed ID: 25450603
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Structural basis for activity of TRIC counter-ion channels in calcium release.
    Wang XH; Su M; Gao F; Xie W; Zeng Y; Li DL; Liu XL; Zhao H; Qin L; Li F; Liu Q; Clarke OB; Lam SM; Shui GH; Hendrickson WA; Chen YH
    Proc Natl Acad Sci U S A; 2019 Mar; 116(10):4238-4243. PubMed ID: 30770441
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of a Recurrent TMEM38B Gene Deletion Associated with Recessive Osteogenesis Imperfecta.
    Ramzan K; Alotaibi M; Huma R; Afzal S
    Discoveries (Craiova); 2021 Mar; 9(1):e124. PubMed ID: 34036147
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mineral particle size in children with osteogenesis imperfecta type I is not increased independently of specific collagen mutations.
    Fratzl-Zelman N; Schmidt I; Roschger P; Glorieux FH; Klaushofer K; Fratzl P; Rauch F; Wagermaier W
    Bone; 2014 Mar; 60():122-8. PubMed ID: 24296239
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Crystal structures of the TRIC trimeric intracellular cation channel orthologues.
    Kasuya G; Hiraizumi M; Maturana AD; Kumazaki K; Fujiwara Y; Liu K; Nakada-Nakura Y; Iwata S; Tsukada K; Komori T; Uemura S; Goto Y; Nakane T; Takemoto M; Kato HE; Yamashita K; Wada M; Ito K; Ishitani R; Hattori M; Nureki O
    Cell Res; 2016 Dec; 26(12):1288-1301. PubMed ID: 27909292
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular findings in Brazilian patients with osteogenesis imperfecta.
    Reis FC; Alexandrino F; Steiner CE; Norato DY; Cavalcanti DP; Sartorato EL
    J Appl Genet; 2005; 46(1):105-8. PubMed ID: 15741671
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Type V osteogenesis imperfecta: a new form of brittle bone disease.
    Glorieux FH; Rauch F; Plotkin H; Ward L; Travers R; Roughley P; Lalic L; Glorieux DF; Fassier F; Bishop NJ
    J Bone Miner Res; 2000 Sep; 15(9):1650-8. PubMed ID: 10976985
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Recessive osteogenesis imperfecta: clinical, radiological, and molecular findings.
    Rohrbach M; Giunta C
    Am J Med Genet C Semin Med Genet; 2012 Aug; 160C(3):175-89. PubMed ID: 22791419
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A nonclassical IFITM5 mutation located in the coding region causes severe osteogenesis imperfecta with prenatal onset.
    Hoyer-Kuhn H; Semler O; Garbes L; Zimmermann K; Becker J; Wollnik B; Schoenau E; Netzer C
    J Bone Miner Res; 2014 Jun; 29(6):1387-91. PubMed ID: 24293101
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Osteogenesis imperfecta: prospects for molecular therapeutics.
    Forlino A; Marini JC
    Mol Genet Metab; 2000; 71(1-2):225-32. PubMed ID: 11001814
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta.
    Sillence DO; Ritchie HE; Dibbayawan T; Eteson D; Brown K
    Am J Med Genet; 1993 Jan; 45(2):276-83. PubMed ID: 8456819
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Osteogenesis imperfecta at the beginning of bone and joint decade.
    Primorac D; Rowe DW; Mottes M; Barisić I; Anticević D; Mirandola S; Gomez Lira M; Kalajzić I; Kusec V; Glorieux FH
    Croat Med J; 2001 Aug; 42(4):393-415. PubMed ID: 11471191
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.
    Hartikka H; Kuurila K; Körkkö J; Kaitila I; Grénman R; Pynnönen S; Hyland JC; Ala-Kokko L
    Hum Mutat; 2004 Aug; 24(2):147-54. PubMed ID: 15241796
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.