Can the profile of extracellular vesicles (EVs) reflect the disease states of patients with Gaucher disease and GBA1 carriers with or without Parkinson's disease?

被引：0
|
作者：
Gleason, Adenrele M. [1 ]
机构：
[1] NHGRI, Natl Inst Hlth, Bethesda, MD 20892 USA
来源：
MOLECULAR GENETICS AND METABOLISM | 2022年 / 135卷 / 02期
关键词：
D O I：
10.1016/j.ymgme.2021.11.115
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
100
引用
收藏
页码：S48 / S48
页数：1
相关论文
共 50 条
  • [21] Experience in Genetic Counseling for GBA1 Variants in Parkinson's Disease
    den Heijer, Jonas M.
    van Hilten, Jacobus J.
    Kievit, Anneke J. A.
    Bonifati, Vincenzo
    Groeneveld, Geert Jan
    MOVEMENT DISORDERS CLINICAL PRACTICE, 2021, 8 (01): : 33 - 36
  • [22] GBA1 and The Immune System: A Potential Role in Parkinson's Disease?
    Al-Azzawi, Zaid A. M.
    Arfaie, Saman
    Gan-Or, Ziv
    JOURNAL OF PARKINSONS DISEASE, 2022, 12 : S53 - S64
  • [23] Rare GBA1 genotype associated with severe bone disease in Gaucher disease type 1
    Paskulin, Livia D'Avila
    Starosta, Rodrigo Tzovenos
    Zizemer, Vitoria Schutt
    Basgalupp, Suelen
    Bertholdo, Debora
    e Vairo, Filippo Pinto
    Siebert, Marina
    Michelin-Tirelli, Kristiane
    Doederlein Schwartz, Ida Vanessa
    MOLECULAR GENETICS AND METABOLISM REPORTS, 2019, 21
  • [24] Lysosomal β-glucosidase (GBA1) and non-lysosomal β-glucosidase (GBA2): Potential involvement in the pathogenesis of Gaucher disease/Parkinson disease
    Burke, Derek G.
    Heales, Simon J.
    Vellodi, Ashok
    MOLECULAR GENETICS AND METABOLISM, 2015, 114 (02) : S26 - S26
  • [25] Revisiting the diagnosis of Gaucher disease in a family with multiple GBA1 variants
    Ryan, Emory
    Tayebi, Nahid
    D'Souza, Andrea
    Lopez, Grisel
    Lichtenberg, Jens
    Sidransky, Ellen
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (10) : 2647 - 2650
  • [26] Increased glucosylsphingosine levels and Gaucher disease in GBA1-associated Parkinson ' s disease
    Marano, Massimo
    Zizzo, Carmela
    Malaguti, Maria Chiara
    Bacchin, Ruggero
    Cavallieri, Francesco
    De Micco, Rosa
    Spagnolo, Francesca
    Bentivoglio, Anna Rita
    Schirinzi, Tommaso
    Bovenzi, Roberta
    Ramat, Silvia
    Erro, Roberto
    Sorrentino, Cristiano
    Sucapane, Patrizia
    Pilotto, Andrea
    Lupini, Alessandro
    Magliozzi, Alessandro
    Di Vico, Ilaria
    Carecchio, Miryam
    Bonato, Giulia
    Cilia, Roberto
    Colucci, Fabiana
    Tamma, Filippo
    Caputo, Elena
    Mostile, Giovanni
    Arabia, Gennarina
    Modugno, Nicola
    Zibetti, Maurizio
    Ceravolo, Maria Gabriella
    Tambasco, Nicola
    Cossu, Giovanni
    Valzania, Franco
    Manganotti, Paolo
    Di Lazzaro, Vincenzo
    Zappia, Mario
    Fabbrini, Giovanni
    Tinazzi, Michele
    Tessitore, Alessandro
    Duro, Giovanni
    Di Fonzo, Alessio
    PARKINSONISM & RELATED DISORDERS, 2024, 124
  • [27] Biochemical markers of glucocerebrosidase (GCase) deficiency in primary macrophages derived from GBA1 mutation carriers with and without Parkinson's disease
    Pchelina, S.
    Kopytova, A.
    Nikolaev, M.
    Emelyanov, A.
    Baydakova, G.
    Usenko, T.
    Izymchenko, A.
    Bogdanova, D.
    Senkevich, K.
    Miliukhina, I.
    Zakharova, Y.
    MOVEMENT DISORDERS, 2022, 37 : S573 - S573
  • [28] Prevalence of Parkinson Disease in Patients and Obligate Carriers of Gaucher Disease
    Becker, Joanna G.
    Pastores, Gregory M.
    Ferraris, Marissa
    Graber, Jerome
    Kolodny, E. H.
    Sathe, Swati
    NEUROLOGY, 2010, 74 (09) : A105 - A105
  • [29] The role of GBA1 mutations in the relationship between GBA1 and alpha-synuclein in Parkinson disease
    Smith, L.
    Gegg, M.
    Chau, D.
    Schapira, A. H. V.
    MOVEMENT DISORDERS, 2022, 37 : S595 - S595
  • [30] GBA1 in Parkinson's disease: variant detection and pathogenicity scoring matters
    Gabbert, Carolin
    Schaake, Susen
    Lueth, Theresa
    Much, Christoph
    Klein, Christine
    Aasly, Jan O.
    Farrer, Matthew J.
    Trinh, Joanne
    BMC GENOMICS, 2023, 24 (01)
12345