Mia Horowitz

Tel Aviv University — Israel

Biochemistry, Genetics and Molecular Biology · Life Sciences

47h-index6.3kcitations141works10.32yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Cellular transport and secretion(75), Lysosomal Storage Disorders Research(74), Glycosylation and Glycoproteins Research(33), Carbohydrate Chemistry and Synthesis(18), Studies on Chitinases and Chitosanases(8)

Publications140 total

Functional Analysis of Human GBA1 Missense Mutations in Drosophila: Insights into Gaucher Disease Pathogenesis and Phenotypic Consequences
Cells·2024· 3 citedOpen Access
GBA1-Associated Parkinson’s Disease Is a Distinct Entity
International Journal of Molecular Sciences·2024· 28 citedOpen Access
Studies on the possible interplay between and genes in Parkinson's disease using models
Molecular Genetics and Metabolism·2024
Animal Models for the Study of Gaucher Disease
International Journal of Molecular Sciences·2023· 10 citedOpen Access
Lysosomal functions and dysfunctions: Molecular and cellular mechanisms underlying Gaucher disease and its association with Parkinson disease
Advanced Drug Delivery Reviews·2022· 51 cited
Modeling misfolding of human disease-causing lysosomal enzymes in as means to test therapeutic modalities
Molecular Genetics and Metabolism·2022
The Uncovered Function of the Drosophila GBA1a-Encoded Protein
Cells·2021· 8 citedOpen Access
Misfolding of Lysosomal α-Galactosidase a in a Fly Model and Its Alleviation by the Pharmacological Chaperone Migalastat
International Journal of Molecular Sciences·2020· 20 citedOpen Access
Inflammation and its alleviation in a fly model for neuronopathic Gaucher disease
Molecular Genetics and Metabolism·2020
International Conference on Glycobiology- The contribution of mutant GBA alleles to the development of Parkinson′s disease in carriers of Gaucher disease mutations
HAL (Le Centre pour la Communication Scientifique Directe)·2020
The contribution of mutant GBA alleles to the development of Parkinsonâ?²s disease in carriers of Gaucher disease mutations
Journal of Stem Cell Biology and Transplantation·2020
Drosophila melanogaster Mutated in its GBA1b Ortholog Recapitulates Neuronopathic Gaucher Disease
Journal of Clinical Medicine·2019· 38 citedOpen Access
The fruit fly Drosophila melanogaster as a model to study Gaucher disease
Molecular Genetics and Metabolism·2019
The effect of mutant GBA1 on accumulation and aggregation of α-synuclein
Human Molecular Genetics·2019· 43 cited
Quantitative analysis of recombinant glucocerebrosidase brain delivery via lipid nanoparticles
Nano Futures·2018· 5 cited
NEK3-mediated SNAP29 phosphorylation modulates its membrane association and SNARE fusion dependent processes
Biochemical and Biophysical Research Communications·2018· 9 cited
The contribution of mutant glucocerebrosidase to the aggregation of alpha synuclein
Molecular Genetics and Metabolism·2018
NEK3-mediated serine 105 phosphorylation of SNAP29 modulates its membrane association and SNARE fusion dependent processes
European Journal of Experimental Biology·2017
Correction: Past1 Modulates Drosophila Eye Development
PLoS ONE·2017Open Access
Past1 Modulates Drosophila Eye Development
PLoS ONE·2017· 2 citedOpen Access
page 1 of 7Next →

Frequent Co-authors

Debora Rapaport(10), Eli Sprecher(6), Ari Zimran(6), Akemi Ishida‐Yamamoto(5), Gali Maor(5), Nurit Eyal(5), Metsada Pasmanik‐Chor(5), Sylvia Wilder(4), Ofer Sarig(4), Idit Ron(4), Aya Abrahamov(4), Ari Zimran(4), Edwin H. Kolodny(4), Emilia Galperin(4), Orly Reiner(3), Andrea Gat(3), Richard N. Bergman(3), Yosef Aloni(3), Orgad Laub(3), Inna Bendikov-Bar(3)