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Journal Abstract Search

153 related items for PubMed ID: 22805531

  • 21. Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti.
    Bal E, Laplantine E, Hamel Y, Dubosclard V, Boisson B, Pescatore A, Picard C, Hadj-Rabia S, Royer G, Steffann J, Bonnefont JP, Ursini VM, Vabres P, Munnich A, Casanova JL, Bodemer C, Weil R, Agou F, Smahi A.
    J Allergy Clin Immunol; 2017 Dec; 140(6):1671-1682.e2. PubMed ID: 28249776
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  • 22. Biogenesis and significance of central nervous system myelin.
    Paz Soldán MM, Pirko I.
    Semin Neurol; 2012 Feb; 32(1):9-14. PubMed ID: 22422202
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  • 23. Strength of ERK1/2 MAPK Activation Determines Its Effect on Myelin and Axonal Integrity in the Adult CNS.
    Ishii A, Furusho M, Dupree JL, Bansal R.
    J Neurosci; 2016 Jun 15; 36(24):6471-87. PubMed ID: 27307235
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  • 24. Nerve impulses regulate myelination through purinergic signalling.
    Fields RD.
    Novartis Found Symp; 2006 Jun 15; 276():148-58; discussion 158-61, 233-7, 275-81. PubMed ID: 16805428
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  • 27. Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.
    El-Hattab AW, Fang P, Jin W, Hughes JR, Gibson JB, Patel GS, Grange DK, Manwaring LP, Patel A, Stankiewicz P, Cheung SW.
    J Med Genet; 2011 Dec 15; 48(12):840-50. PubMed ID: 21984752
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  • 29. Dual-mode modulation of Smad signaling by Smad-interacting protein Sip1 is required for myelination in the central nervous system.
    Weng Q, Chen Y, Wang H, Xu X, Yang B, He Q, Shou W, Chen Y, Higashi Y, van den Berghe V, Seuntjens E, Kernie SG, Bukshpun P, Sherr EH, Huylebroeck D, Lu QR.
    Neuron; 2012 Feb 23; 73(4):713-28. PubMed ID: 22365546
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  • 30. Classical NF-κB activation impairs skeletal muscle oxidative phenotype by reducing IKK-α expression.
    Remels AH, Gosker HR, Langen RC, Polkey M, Sliwinski P, Galdiz J, van den Borst B, Pansters NA, Schols AM.
    Biochim Biophys Acta; 2014 Feb 23; 1842(2):175-85. PubMed ID: 24215713
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  • 39. Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability.
    Nguyen HH, Pham VA, Barcia G, Malan V, Nguyen KLT, Ngo DN, Nguyen TH, Landrieu P, Colleaux L, Nong VH, Nguyen LS.
    Am J Med Genet A; 2018 Sep 23; 176(9):1981-1984. PubMed ID: 30178921
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  • 40. Xq26.1-26.3 duplication including MOSPD1 and GPC3 identified in boy with short stature and double outlet right ventricle.
    Hirota Y, Minami T, Sato T, Yokomizo A, Matsumoto A, Goto M, Jinbo E, Yamamgata T.
    Am J Med Genet A; 2017 Sep 23; 173(9):2446-2450. PubMed ID: 28636109
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