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 *

138 related articles for article (PubMed ID: 33334662)

  • 1. Impaired NDRG1 functions in Schwann cells cause demyelinating neuropathy in a dog model of Charcot-Marie-Tooth type 4D.
    Skedsmo FS; Espenes A; Tranulis MA; Matiasek K; Gunnes G; Bjerkås I; Moe L; Røed SS; Berendt M; Fredholm M; Rohdin C; Shelton GD; Bruheim P; Stafsnes MH; Bartosova Z; Hermansen LC; Stigen Ø; Jäderlund KH
    Neuromuscul Disord; 2021 Jan; 31(1):56-68. PubMed ID: 33334662
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cell and context-dependent sorting of neuropathy-associated protein NDRG1 - insights from canine tissues and primary Schwann cell cultures.
    Skedsmo FS; Tranulis MA; Espenes A; Prydz K; Matiasek K; Gunnes G; Hermansen LC; Jäderlund KH
    BMC Vet Res; 2019 Apr; 15(1):121. PubMed ID: 31029158
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy.
    Drögemüller C; Becker D; Kessler B; Kemter E; Tetens J; Jurina K; Jäderlund KH; Flagstad A; Perloski M; Lindblad-Toh K; Matiasek K
    PLoS One; 2010 Jun; 5(6):e11258. PubMed ID: 20582309
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ndrg1-deficient mice exhibit a progressive demyelinating disorder of peripheral nerves.
    Okuda T; Higashi Y; Kokame K; Tanaka C; Kondoh H; Miyata T
    Mol Cell Biol; 2004 May; 24(9):3949-56. PubMed ID: 15082788
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ndrg1 in development and maintenance of the myelin sheath.
    King RH; Chandler D; Lopaticki S; Huang D; Blake J; Muddle JR; Kilpatrick T; Nourallah M; Miyata T; Okuda T; Carter KW; Hunter M; Angelicheva D; Morahan G; Kalaydjieva L
    Neurobiol Dis; 2011 Jun; 42(3):368-80. PubMed ID: 21303696
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy.
    Bruun CS; Jäderlund KH; Berendt M; Jensen KB; Spodsberg EH; Gredal H; Shelton GD; Mickelson JR; Minor KM; Lohi H; Bjerkås I; Stigen O; Espenes A; Rohdin C; Edlund R; Ohlsson J; Cizinauskas S; Leifsson PS; Drögemüller C; Moe L; Cirera S; Fredholm M
    PLoS One; 2013; 8(2):e54547. PubMed ID: 23393557
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tongue atrophy as a neurological finding in hereditary polyneuropathy in Alaskan malamutes.
    Hultman J; Jäderlund KH; Moe L; Espenes A; Skedsmo FS
    J Vet Intern Med; 2022 Mar; 36(2):672-678. PubMed ID: 35019187
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Aberrant Neuregulin 1/ErbB Signaling in Charcot-Marie-Tooth Type 4D Disease.
    Jiang LT; Chen YH; Huang JH; Tong WF; Jin LJ; Li LX
    Mol Cell Biol; 2022 Jul; 42(7):e0055921. PubMed ID: 35708320
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification and functional characterization of two missense mutations in NDRG1 associated with Charcot-Marie-Tooth disease type 4D.
    Li LX; Liu GL; Liu ZJ; Lu C; Wu ZY
    Hum Mutat; 2017 Nov; 38(11):1569-1578. PubMed ID: 28776325
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom.
    Berger P; Sirkowski EE; Scherer SS; Suter U
    Neurobiol Dis; 2004 Nov; 17(2):290-9. PubMed ID: 15474366
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Re-emergence of hereditary polyneuropathy in Scandinavian Alaskan malamute dogs-old enemy or new entity? A case series.
    Jäderlund KH; Rohdin C; Berendt M; Stigen Ø; Fredholm M; Espenes A; Bjerkås I; Moe L
    Acta Vet Scand; 2017 May; 59(1):26. PubMed ID: 28464941
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot-Marie-Tooth disease type 1C.
    Lee SM; Sha D; Mohammed AA; Asress S; Glass JD; Chin LS; Li L
    Hum Mol Genet; 2013 May; 22(9):1755-70. PubMed ID: 23359569
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis.
    Hahn AF; Ainsworth PJ; Bolton CF; Bilbao JM; Vallat JM
    Acta Neuropathol; 2001 Feb; 101(2):129-39. PubMed ID: 11271367
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 15. N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.
    Kalaydjieva L; Gresham D; Gooding R; Heather L; Baas F; de Jonge R; Blechschmidt K; Angelicheva D; Chandler D; Worsley P; Rosenthal A; King RH; Thomas PK
    Am J Hum Genet; 2000 Jul; 67(1):47-58. PubMed ID: 10831399
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exclusive expression of the Rab11 effector SH3TC2 in Schwann cells links integrin-α6 and myelin maintenance to Charcot-Marie-Tooth disease type 4C.
    Vijay S; Chiu M; Dacks JB; Roberts RC
    Biochim Biophys Acta; 2016 Jul; 1862(7):1279-90. PubMed ID: 27068304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-Lom.
    Piscosquito G; Magri S; Saveri P; Milani M; Ciano C; Farina L; Taroni F; Pareyson D
    J Peripher Nerv Syst; 2017 Mar; 22(1):47-50. PubMed ID: 27982524
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement.
    Echaniz-Laguna A; Degos B; Bonnet C; Latour P; Hamadouche T; Lévy N; Leheup B
    Neuromuscul Disord; 2007 Feb; 17(2):163-8. PubMed ID: 17142040
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease.
    Hunter M; Bernard R; Freitas E; Boyer A; Morar B; Martins IJ; Tournev I; Jordanova A; Guergelcheva V; Ishpekova B; Kremensky I; Nicholson G; Schlotter B; Lochmüller H; Voit T; Colomer J; Thomas PK; Levy N; Kalaydjieva L
    Hum Mutat; 2003 Aug; 22(2):129-35. PubMed ID: 12872253
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease.
    Niemann A; Berger P; Suter U
    Neuromolecular Med; 2006; 8(1-2):217-42. PubMed ID: 16775378
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.