BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 29366908)

  • 21. K-Cl cotransport in red blood cells from patients with KCC3 isoform mutants.
    Lauf PK; Adragna NC; Dupre N; Bouchard JP; Rouleau GA
    Biochem Cell Biol; 2006 Dec; 84(6):1034-44. PubMed ID: 17215889
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Electroneutral cation-chloride cotransporters in the central nervous system.
    Mercado A; Mount DB; Gamba G
    Neurochem Res; 2004 Jan; 29(1):17-25. PubMed ID: 14992262
    [TBL] [Abstract][Full Text] [Related]  

  • 23. KCC3-dependent chloride extrusion in adult sensory neurons.
    Lucas O; Hilaire C; Delpire E; Scamps F
    Mol Cell Neurosci; 2012 Jul; 50(3-4):211-20. PubMed ID: 22609694
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular insights into the normal operation, regulation, and multisystemic roles of K
    Garneau AP; Marcoux AA; Frenette-Cotton R; Mac-Way F; Lavoie JL; Isenring P
    Am J Physiol Cell Physiol; 2017 Nov; 313(5):C516-C532. PubMed ID: 28814402
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome.
    Uyanik G; Elcioglu N; Penzien J; Gross C; Yilmaz Y; Olmez A; Demir E; Wahl D; Scheglmann K; Winner B; Bogdahn U; Topaloglu H; Hehr U; Winkler J
    Neurology; 2006 Apr; 66(7):1044-8. PubMed ID: 16606917
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family.
    Mount DB; Mercado A; Song L; Xu J; George AL; Delpire E; Gamba G
    J Biol Chem; 1999 Jun; 274(23):16355-62. PubMed ID: 10347194
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold.
    Boettger T; Rust MB; Maier H; Seidenbecher T; Schweizer M; Keating DJ; Faulhaber J; Ehmke H; Pfeffer C; Scheel O; Lemcke B; Horst J; Leuwer R; Pape HC; Völkl H; Hübner CA; Jentsch TJ
    EMBO J; 2003 Oct; 22(20):5422-34. PubMed ID: 14532115
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Expanding the phenotype of
    Bogdanova-Mihaylova P; McNamara P; Burton-Jones S; Murphy SM
    BMJ Case Rep; 2021 Oct; 14(10):. PubMed ID: 34706912
    [TBL] [Abstract][Full Text] [Related]  

  • 29. N-terminal serine dephosphorylation is required for KCC3 cotransporter full activation by cell swelling.
    Melo Z; de los Heros P; Cruz-Rangel S; Vázquez N; Bobadilla NA; Pasantes-Morales H; Alessi DR; Mercado A; Gamba G
    J Biol Chem; 2013 Nov; 288(44):31468-76. PubMed ID: 24043619
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Neurogenic mechanisms contribute to hypertension in mice with disruption of the K-Cl cotransporter KCC3.
    Rust MB; Faulhaber J; Budack MK; Pfeffer C; Maritzen T; Didié M; Beck FX; Boettger T; Schubert R; Ehmke H; Jentsch TJ; Hübner CA
    Circ Res; 2006 Mar; 98(4):549-56. PubMed ID: 16424367
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The KCC3 cotransporter as a therapeutic target for peripheral neuropathy.
    Delpire E; Kahle KT
    Expert Opin Ther Targets; 2017 Feb; 21(2):113-116. PubMed ID: 28019725
    [No Abstract]   [Full Text] [Related]  

  • 32. A trafficking-deficient mutant of KCC3 reveals dominant-negative effects on K-Cl cotransport function.
    Ding J; Ponce-Coria J; Delpire E
    PLoS One; 2013; 8(4):e61112. PubMed ID: 23593405
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.
    Dupré N; Howard HC; Mathieu J; Karpati G; Vanasse M; Bouchard JP; Carpenter S; Rouleau GA
    Ann Neurol; 2003 Jul; 54(1):9-18. PubMed ID: 12838516
    [TBL] [Abstract][Full Text] [Related]  

  • 34. First case of Roma ethnic origin with Andermann syndrome: A novel frameshift mutation in exon 20 of SLC12A6 gene.
    Pacheva I; Todorov T; Halil Z; Yordanova R; Todorova A; Geneva I; Galabova F; Ivanov I
    Am J Med Genet A; 2019 Jun; 179(6):1020-1024. PubMed ID: 30868738
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial progressive sensorimotor neuropathy with agenesis of the corpus callosum (Andermann syndrome): a clinical, neuroradiological and histopathological study.
    Deleu D; Bamanikar SA; Muirhead D; Louon A
    Eur Neurol; 1997; 37(2):104-9. PubMed ID: 9058066
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelination.
    Omer S; Jin SC; Koumangoye R; Robert SM; Duran D; Nelson-Williams C; Huttner A; DiLuna M; Kahle KT; Delpire E
    Clin Genet; 2021 Aug; 100(2):176-186. PubMed ID: 33904160
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular cloning and functional characterization of KCC3, a new K-Cl cotransporter.
    Race JE; Makhlouf FN; Logue PJ; Wilson FH; Dunham PB; Holtzman EJ
    Am J Physiol; 1999 Dec; 277(6):C1210-9. PubMed ID: 10600773
    [TBL] [Abstract][Full Text] [Related]  

  • 38. IGF-1 upregulates electroneutral K-Cl cotransporter KCC3 and KCC4 which are differentially required for breast cancer cell proliferation and invasiveness.
    Hsu YM; Chou CY; Chen HH; Lee WY; Chen YF; Lin PW; Alper SL; Ellory JC; Shen MR
    J Cell Physiol; 2007 Mar; 210(3):626-36. PubMed ID: 17133354
    [TBL] [Abstract][Full Text] [Related]  

  • 39. KCC3a, a Strong Candidate Pathway for K
    Ferdaus MZ; Terker AS; Koumangoye R; Delpire E
    Front Cell Dev Biol; 2022; 10():931326. PubMed ID: 35874803
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Erythroid-specific inactivation of Slc12a6/Kcc3 by EpoR promoter-driven Cre expression reduces K-Cl cotransport activity in mouse erythrocytes.
    Shmukler BE; Rivera A; Nishimura K; Hsu A; Wohlgemuth JG; Dlott JS; Michael Snyder L; Brugnara C; Alper SL
    Physiol Rep; 2022 Mar; 10(5):e15186. PubMed ID: 35274823
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.