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 *

383 related articles for article (PubMed ID: 27638887)

  • 1. Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation.
    Renvoisé B; Malone B; Falgairolle M; Munasinghe J; Stadler J; Sibilla C; Park SH; Blackstone C
    Hum Mol Genet; 2016 Dec; 25(23):5111-5125. PubMed ID: 27638887
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons.
    Zhu PP; Hung HF; Batchenkova N; Nixon-Abell J; Henderson J; Zheng P; Renvoisé B; Pang S; Xu CS; Saalfeld S; Funke J; Xie Y; Svara F; Hess HF; Blackstone C
    Hum Mol Genet; 2022 Aug; 31(16):2779-2795. PubMed ID: 35348668
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network.
    Park SH; Zhu PP; Parker RL; Blackstone C
    J Clin Invest; 2010 Apr; 120(4):1097-110. PubMed ID: 20200447
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Functional mutation analysis provides evidence for a role of REEP1 in lipid droplet biology.
    Falk J; Rohde M; Bekhite MM; Neugebauer S; Hemmerich P; Kiehntopf M; Deufel T; Hübner CA; Beetz C
    Hum Mutat; 2014 Apr; 35(4):497-504. PubMed ID: 24478229
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts.
    Lim Y; Cho IT; Schoel LJ; Cho G; Golden JA
    Ann Neurol; 2015 Nov; 78(5):679-96. PubMed ID: 26201691
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.
    Fink JK
    Acta Neuropathol; 2013 Sep; 126(3):307-28. PubMed ID: 23897027
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
    Elert-Dobkowska E; Stepniak I; Krysa W; Rajkiewicz M; Rakowicz M; Sobanska A; Rudzinska M; Wasielewska A; Pilch J; Kubalska J; Lipczynska-Lojkowska W; Kulczycki J; Kurdziel K; Sikorska A; Beetz C; Zaremba J; Sulek A
    J Neurol Sci; 2015 Dec; 359(1-2):35-9. PubMed ID: 26671083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary spastic paraplegia SPG4: what is known and not known about the disease.
    Solowska JM; Baas PW
    Brain; 2015 Sep; 138(Pt 9):2471-84. PubMed ID: 26094131
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A spastic paraplegia mouse model reveals REEP1-dependent ER shaping.
    Beetz C; Koch N; Khundadze M; Zimmer G; Nietzsche S; Hertel N; Huebner AK; Mumtaz R; Schweizer M; Dirren E; Karle KN; Irintchev A; Alvarez V; Redies C; Westermann M; Kurth I; Deufel T; Kessels MM; Qualmann B; Hübner CA
    J Clin Invest; 2013 Oct; 123(10):4273-82. PubMed ID: 24051375
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Seipinopathy: a novel endoplasmic reticulum stress-associated disease.
    Ito D; Suzuki N
    Brain; 2009 Jan; 132(Pt 1):8-15. PubMed ID: 18790819
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP).
    Hewamadduma C; McDermott C; Kirby J; Grierson A; Panayi M; Dalton A; Rajabally Y; Shaw P
    Neurogenetics; 2009 Apr; 10(2):105-10. PubMed ID: 19034539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A complete overview of REEP1: old and new insights on its role in hereditary spastic paraplegia and neurodegeneration.
    Guglielmi A
    Rev Neurosci; 2020 May; 31(4):351-362. PubMed ID: 31913854
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia.
    Mou Y; Dong Y; Chen Z; Denton KR; Duff MO; Blackstone C; Zhang SC; Li XJ
    Acta Neuropathol Commun; 2020 Dec; 8(1):214. PubMed ID: 33287888
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31).
    Schlang KJ; Arning L; Epplen JT; Stemmler S
    BMC Med Genet; 2008 Jul; 9():71. PubMed ID: 18644145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12.
    Montenegro G; Rebelo AP; Connell J; Allison R; Babalini C; D'Aloia M; Montieri P; Schüle R; Ishiura H; Price J; Strickland A; Gonzalez MA; Baumbach-Reardon L; Deconinck T; Huang J; Bernardi G; Vance JM; Rogers MT; Tsuji S; De Jonghe P; Pericak-Vance MA; Schöls L; Orlacchio A; Reid E; Züchner S
    J Clin Invest; 2012 Feb; 122(2):538-44. PubMed ID: 22232211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia.
    McCorquodale DS; Ozomaro U; Huang J; Montenegro G; Kushman A; Citrigno L; Price J; Speziani F; Pericak-Vance MA; Züchner S
    Clin Genet; 2011 Jun; 79(6):523-30. PubMed ID: 20718791
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Function of seipin: new insights from Bscl2/seipin knockout mouse models.
    Dollet L; Magré J; Cariou B; Prieur X
    Biochimie; 2014 Jan; 96():166-72. PubMed ID: 23831461
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology.
    Szymanski KM; Binns D; Bartz R; Grishin NV; Li WP; Agarwal AK; Garg A; Anderson RG; Goodman JM
    Proc Natl Acad Sci U S A; 2007 Dec; 104(52):20890-5. PubMed ID: 18093937
    [TBL] [Abstract][Full Text] [Related]  

  • 19. REEPing the benefits of an animal model of hereditary spastic paraplegia.
    Deutch AY; Hedera P; Colbran RJ
    J Clin Invest; 2013 Oct; 123(10):4134-6. PubMed ID: 24051371
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protrudin regulates endoplasmic reticulum morphology and function associated with the pathogenesis of hereditary spastic paraplegia.
    Hashimoto Y; Shirane M; Matsuzaki F; Saita S; Ohnishi T; Nakayama KI
    J Biol Chem; 2014 May; 289(19):12946-61. PubMed ID: 24668814
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.