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 *

169 related articles for article (PubMed ID: 35708320)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. A novel homozygous NDRG1 mutation in a Chinese patient with Charcot-Marie-Tooth disease 4D.
    Chen B; Niu S; Chen N; Pan H; Wang X; Zhang Z
    J Clin Neurosci; 2018 Jul; 53():231-234. PubMed ID: 29724652
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.
    El-Bazzal L; Ghata A; Estève C; Gadacha J; Quintana P; Castro C; Roeckel-Trévisiol N; Lembo F; Lenfant N; Mégarbané A; Borg JP; Lévy N; Bartoli M; Poitelon Y; Roubertoux PL; Delague V; Bernard-Marissal N
    Brain; 2023 May; 146(5):1844-1858. PubMed ID: 36314052
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CMT4D (NDRG1 mutation): genotype-phenotype correlations.
    Ricard E; Mathis S; Magdelaine C; Delisle MB; Magy L; Funalot B; Vallat JM
    J Peripher Nerv Syst; 2013 Sep; 18(3):261-5. PubMed ID: 24028195
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NDRG1 functions in LDL receptor trafficking by regulating endosomal recycling and degradation.
    Pietiäinen V; Vassilev B; Blom T; Wang W; Nelson J; Bittman R; Bäck N; Zelcer N; Ikonen E
    J Cell Sci; 2013 Sep; 126(Pt 17):3961-71. PubMed ID: 23813961
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disruption of Endosomal Sorting in Schwann Cells Leads to Defective Myelination and Endosomal Abnormalities Observed in Charcot-Marie-Tooth Disease.
    McLean JW; Wilson JA; Tian T; Watson JA; VanHart M; Bean AJ; Scherer SS; Crossman DK; Ubogu E; Wilson SM
    J Neurosci; 2022 Jun; 42(25):5085-5101. PubMed ID: 35589390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D.
    Pravinbabu P; Holla VV; Phulpagar P; Kamble N; Netravathi M; Yadav R; Pal PK; Muthusamy B
    Neurol Sci; 2022 Jul; 43(7):4463-4472. PubMed ID: 35149926
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sh3tc2 deficiency affects neuregulin-1/ErbB signaling.
    Gouttenoire EA; Lupo V; Calpena E; Bartesaghi L; Schüpfer F; Médard JJ; Maurer F; Beckmann JS; Senderek J; Palau F; Espinós C; Chrast R
    Glia; 2013 Jul; 61(7):1041-51. PubMed ID: 23553667
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dysregulation of ErbB Receptor Trafficking and Signaling in Demyelinating Charcot-Marie-Tooth Disease.
    Lee SM; Chin LS; Li L
    Mol Neurobiol; 2017 Jan; 54(1):87-100. PubMed ID: 26732592
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Identification and Characterization of Novel Founder Mutations in
    Atkinson D; Chamova T; Candayan A; Kastreva K; Asenov O; Litvinenko I; Estrada-Cuzcano A; De Vriendt E; Kukushev G; Tournev I; Jordanova A
    Int J Mol Sci; 2024 Aug; 25(16):. PubMed ID: 39201732
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Schwann cell-specific deletion of the endosomal PI 3-kinase Vps34 leads to delayed radial sorting of axons, arrested myelination, and abnormal ErbB2-ErbB3 tyrosine kinase signaling.
    Logan AM; Mammel AE; Robinson DC; Chin AL; Condon AF; Robinson FL
    Glia; 2017 Sep; 65(9):1452-1470. PubMed ID: 28617998
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Soluble Neuregulin1 is strongly up-regulated in the rat model of Charcot-Marie-Tooth 1A disease.
    Fornasari BE; Ronchi G; Pascal D; Visigalli D; Capodivento G; Nobbio L; Perroteau I; Schenone A; Geuna S; Gambarotta G
    Exp Biol Med (Maywood); 2018 Feb; 243(4):370-374. PubMed ID: 29350067
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NDRG1 is induced by antigen-receptor signaling but dispensable for B and T cell self-tolerance.
    Hodgson R; Xu X; Anzilotti C; Deobagkar-Lele M; Crockford TL; Kepple JD; Cawthorne E; Bhandari A; Cebrian-Serrano A; Wilcock MJ; Davies B; Cornall RJ; Bull KR
    Commun Biol; 2022 Nov; 5(1):1216. PubMed ID: 36357486
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.