Literature DB >> 20620894

[Niemann-Pick C disease: history, current research topics, biological and molecular diagnosis].

Marie T Vanier1.   

Abstract

The main historical steps leading to the concept of Niemann-Pick type C disease as an intracellular lipid and more specifically a cholesterol transport disorder are summarized; the current stage of knowledge and research hypotheses regarding the function of the NPC1 and NPC2 proteins and pathogeny of the cerebral dysfunction are briefly commented. The various approaches for laboratory diagnosis of patients are finally discussed. Copyright (c) 2010 Elsevier Masson SAS. All rights reserved.

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Year:  2010        PMID: 20620894     DOI: 10.1016/S0929-693X(10)70010-5

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  8 in total

Review 1.  The Extending Spectrum of NPC1-Related Human Disorders: From Niemann-Pick C1 Disease to Obesity.

Authors:  Amel Lamri; Marie Pigeyre; William S Garver; David Meyre
Journal:  Endocr Rev       Date:  2018-04-01       Impact factor: 19.871

2.  Relative acidic compartment volume as a lysosomal storage disorder-associated biomarker.

Authors:  Danielle te Vruchte; Anneliese O Speak; Kerri L Wallom; Nada Al Eisa; David A Smith; Christian J Hendriksz; Louise Simmons; Robin H Lachmann; Alison Cousins; Ralf Hartung; Eugen Mengel; Heiko Runz; Michael Beck; Yasmina Amraoui; Jackie Imrie; Elizabeth Jacklin; Kate Riddick; Nicole M Yanjanin; Christopher A Wassif; Arndt Rolfs; Florian Rimmele; Naomi Wright; Clare Taylor; Uma Ramaswami; Timothy M Cox; Caroline Hastings; Xuntian Jiang; Rohini Sidhu; Daniel S Ory; Begona Arias; Mylvaganam Jeyakumar; Daniel J Sillence; James E Wraith; Forbes D Porter; Mario Cortina-Borja; Frances M Platt
Journal:  J Clin Invest       Date:  2014-03       Impact factor: 14.808

Review 3.  The promise and perils of HDAC inhibitors in neurodegeneration.

Authors:  Alessandro Didonna; Puneet Opal
Journal:  Ann Clin Transl Neurol       Date:  2014-12-03       Impact factor: 4.511

4.  Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate Metabolism.

Authors:  Anne Gläser; Franziska Hammerl; Markus H Gräler; Sina M Coldewey; Christin Völkner; Moritz J Frech; Fan Yang; Jiankai Luo; Eric Tönnies; Oliver von Bohlen Und Halbach; Nicola Brandt; Diana Heimes; Anna-Maria Neßlauer; Georg Christoph Korenke; Marta Owczarek-Lipska; John Neidhardt; Arndt Rolfs; Andreas Wree; Martin Witt; Anja Ursula Bräuer
Journal:  Int J Mol Sci       Date:  2020-06-24       Impact factor: 5.923

5.  Different Niemann-Pick C1 Genotypes Generate Protein Phenotypes that Vary in their Intracellular Processing, Trafficking and Localization.

Authors:  Hadeel Shammas; Eva-Maria Kuech; Sandra Rizk; Anibh M Das; Hassan Y Naim
Journal:  Sci Rep       Date:  2019-03-28       Impact factor: 4.379

6.  NPC1 enables cholesterol mobilization during long-term potentiation that can be restored in Niemann-Pick disease type C by CYP46A1 activation.

Authors:  Daniel N Mitroi; Guadalupe Pereyra-Gómez; Beatriz Soto-Huelin; Fernando Senovilla; Toshihide Kobayashi; Jose A Esteban; María Dolores Ledesma
Journal:  EMBO Rep       Date:  2019-09-18       Impact factor: 8.807

7.  NPC1 Deficiency Contributes to Autophagy-Dependent Ferritinophagy in HEI-OC1 Auditory Cells.

Authors:  Lihong Liang; Hongshun Wang; Jun Yao; Qinjun Wei; Yajie Lu; Tianming Wang; Xin Cao
Journal:  Front Mol Biosci       Date:  2022-07-22

8.  NPC1 silent variant induces skipping of exon 11 (p.V562V) and unfolded protein response was found in a specific Niemann-Pick type C patient.

Authors:  Marisa Encarnação; Maria Francisca Coutinho; Soo Min Cho; Maria Teresa Cardoso; Isaura Ribeiro; Paulo Chaves; Juliana Inês Santos; Dulce Quelhas; Lúcia Lacerda; Elisa Leão Teles; Anthony H Futerman; Laura Vilarinho; Sandra Alves
Journal:  Mol Genet Genomic Med       Date:  2020-09-15       Impact factor: 2.183

  8 in total

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