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 *

188 related articles for article (PubMed ID: 37082017)

  • 1. Role of the Connexin C-terminus in skin pattern formation of Zebrafish.
    Usui Y; Watanabe M
    BBA Adv; 2021; 1():100006. PubMed ID: 37082017
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Physiological Characterization of Connexin41.8 and Connexin39.4, Which Are Involved in the Striped Pattern Formation of Zebrafish.
    Watanabe M; Sawada R; Aramaki T; Skerrett IM; Kondo S
    J Biol Chem; 2016 Jan; 291(3):1053-63. PubMed ID: 26598520
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The minimal gap-junction network among melanophores and xanthophores required for stripe pattern formation in zebrafish.
    Usui Y; Aramaki T; Kondo S; Watanabe M
    Development; 2019 Nov; 146(22):. PubMed ID: 31666235
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fish-specific N-terminal domain sequence in Connexin 39.4 plays an important role in zebrafish stripe formation by regulating the opening and closing of gap junctions and hemichannels.
    Watanabe M
    Biochim Biophys Acta Gen Subj; 2023 May; 1867(5):130342. PubMed ID: 36889448
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gap junctions composed of connexins 41.8 and 39.4 are essential for colour pattern formation in zebrafish.
    Irion U; Frohnhöfer HG; Krauss J; Çolak Champollion T; Maischein HM; Geiger-Rudolph S; Weiler C; Nüsslein-Volhard C
    Elife; 2014 Dec; 3():e05125. PubMed ID: 25535837
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterotypic interactions regulate cell shape and density during color pattern formation in zebrafish.
    Mahalwar P; Singh AP; Fadeev A; Nüsslein-Volhard C; Irion U
    Biol Open; 2016 Nov; 5(11):1680-1690. PubMed ID: 27742608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spatiotemporal expression of connexin 39 and -43 during myoblast differentiation in cultured cells and in the mouse embryo.
    von Maltzahn J; Wulf V; Willecke K
    Cell Commun Adhes; 2006; 13(1-2):55-60. PubMed ID: 16613780
    [TBL] [Abstract][Full Text] [Related]  

  • 8. On Biophysical Properties and Sensitivity to Gap Junction Blockers of Connexin 39 Hemichannels Expressed in HeLa Cells.
    Vargas AA; Cisterna BA; Saavedra-Leiva F; Urrutia C; Cea LA; Vielma AH; Gutierrez-Maldonado SE; Martin AJ; Pareja-Barrueto C; Escalona Y; Schmachtenberg O; Lagos CF; Perez-Acle T; Sáez JC
    Front Physiol; 2017; 8():38. PubMed ID: 28232803
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spermidine, but not spermine, is essential for pigment pattern formation in zebrafish.
    Frohnhöfer HG; Geiger-Rudolph S; Pattky M; Meixner M; Huhn C; Maischein HM; Geisler R; Gehring I; Maderspacher F; Nüsslein-Volhard C; Irion U
    Biol Open; 2016 Jun; 5(6):736-44. PubMed ID: 27215328
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Connexin39 deficient mice display accelerated myogenesis and regeneration of skeletal muscle.
    von Maltzahn J; Wulf V; Matern G; Willecke K
    Exp Cell Res; 2011 May; 317(8):1169-78. PubMed ID: 21272575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular cloning, tissue distribution, and hormonal control in the ovary of Cx41 mRNA, a novel Xenopus connexin gene transcript.
    Yoshizaki G; Patiño R
    Mol Reprod Dev; 1995 Sep; 42(1):7-18. PubMed ID: 8562053
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Emerging issues of connexin channels: biophysics fills the gap.
    Harris AL
    Q Rev Biophys; 2001 Aug; 34(3):325-472. PubMed ID: 11838236
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Polyamine sensitivity of gap junctions is required for skin pattern formation in zebrafish.
    Watanabe M; Watanabe D; Kondo S
    Sci Rep; 2012; 2():473. PubMed ID: 22737406
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene.
    Watanabe M; Iwashita M; Ishii M; Kurachi Y; Kawakami A; Kondo S; Okada N
    EMBO Rep; 2006 Sep; 7(9):893-7. PubMed ID: 16845369
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Impaired Cx43 gap junction endocytosis causes morphological and functional defects in zebrafish.
    Hyland C; Mfarej M; Hiotis G; Lancaster S; Novak N; Iovine MK; Falk MM
    Mol Biol Cell; 2021 Oct; 32(20):ar13. PubMed ID: 34379446
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The connexin 30.3 of zebrafish homologue of human connexin 26 may play similar role in the inner ear.
    Chang-Chien J; Yen YC; Chien KH; Li SY; Hsu TC; Yang JJ
    Hear Res; 2014 Jul; 313():55-66. PubMed ID: 24811980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Changing clothes easily: connexin41.8 regulates skin pattern variation.
    Watanabe M; Kondo S
    Pigment Cell Melanoma Res; 2012 May; 25(3):326-30. PubMed ID: 22313791
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The role of the Cx43 C-terminus in GJ plaque formation and internalization.
    Wayakanon P; Bhattacharjee R; Nakahama K; Morita I
    Biochem Biophys Res Commun; 2012 Apr; 420(2):456-61. PubMed ID: 22430144
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Instructive role of melanocytes during pigment pattern formation of the avian skin.
    Inaba M; Jiang TX; Liang YC; Tsai S; Lai YC; Widelitz RB; Chuong CM
    Proc Natl Acad Sci U S A; 2019 Apr; 116(14):6884-6890. PubMed ID: 30886106
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gap Junction in the Teleost Fish Lineage: Duplicated Connexins May Contribute to Skin Pattern Formation and Body Shape Determination.
    Watanabe M
    Front Cell Dev Biol; 2017; 5():13. PubMed ID: 28271062
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.