Profil bibliographique

Justin K. Ichida

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

110Publications signalées

7396Citations signalées

2Affiliations récentes

Institutions déclarées

University of Southern California Broad Center

Domaines associés

Amyotrophic Lateral Sclerosis ResearchPluripotent Stem Cells ResearchNeurogenetic and Muscular Disorders ResearchCRISPR and Genetic EngineeringGenetic Neurodegenerative Diseases

Publications récentes

Accès ouvert 2026 preprintOpenAlex

C9orf72 -associated G4C2 hexanucleotide repeat expression in Drosophila mushroom bodies causes age dependent TDP-43 pathology and dementia relevant phenotypes mediated in part by the glypican Dlp/GPC6

Brijesh Singh Chauhan, Megan Alexandria Brennan, Peter Christen Forstmeier, Yifu Han et autres

0 citationsbioRxiv (Cold Spring Harbor Laboratory)

Accès ouvert 2026 articleOpenAlex

Unveiling alternate pathways for SARS-CoV-2 infection via extracellular vesicle-mediated transfer of ACE2 and TMPRSS2

Martha Rea-Moreno, Lu Tian, Tara N. Tavakol, Min-Chi Yang et autres

3 citationsNature Communications

Accès ouvert 2026 articleOpenAlex

C9orf72 hexanucleotide repeat RNA drives transcriptional dysregulation through genome-wide DNA:RNA hybrid G-quadruplexes

Honghe Liu, Mingming Liu, Yang Liu, Gege Gui et autres

3 citationsNeuron

Accès ouvert 2026 articleOpenAlex

PIKFYVE inhibition mitigates disease in models of diverse forms of ALS

Shu-Ting Hung, Gabriel Linares, Wen-Hsuan Chang, Yunsun Eoh et autres

0 citationsCell

Accès ouvert 2025 articleOpenAlex

The Ku80-p53-SIRT1 axis in DNA damage response contributes to sporadic and familial ALS and FTD

Soojin Lee, Sandra Almeida, Kristine Freude, Justin K. Ichida et autres

2 citationsNature Communications

Accès ouvert 2025 articleOpenAlex

AAV delivery of full-length SYNGAP1 rescues epileptic and behavioral phenotypes in a mouse model of SYNGAP1-related disorders

Meagan A. Quinlan, Rong Guo, Andrew G. Clark, Emily M. Luber et autres

11 citationsMolecular Therapy

Accès ouvert 2025 articleOpenAlex

AAV-mediated exon skipping therapy for Usher syndrome, type 2A

Stéphanie A. Mauriac, Jiyoon Lee, Jingyuan Zhang, Jiahe Jin et autres

2 citationsMolecular Therapy

Accès ouvert 2025 articleOpenAlex

Spatially patterned kidney assembloids recapitulate progenitor self-assembly and enable high-fidelity in vivo disease modeling

Biao Huang, Pedro P. Medina, Jincan He, Zipeng Zeng et autres

20 citationsCell stem cell

Accès ouvert 2025 articleOpenAlex

Elevated tripeptidyl-peptidase 1 corrects multiple disease phenotypes in a mouse model of juvenile neuronal ceroid lipofuscinosis

Whitney Banach‐Petrosky, Katherine E. Larrimore, Elizabeth H Sleat, Allyson Bazer et autres

1 citationMolecular Therapy — Methods & Clinical Development

Accès ouvert 2025 articleOpenAlex

Single-cell polygenic risk scores dissect cellular and molecular heterogeneity of complex human diseases

Sai Zhang, Hantao Shu, Jingtian Zhou, Jasper Rubin-Sigler et autres

13 citationsNature Biotechnology

Accès ouvert 2025 articleOpenAlex

An ALS assembly modulator signature in peripheral blood mononuclear cells: implications for ALS pathophysiology, therapeutics, and diagnostics

Shao Feng Yu, Maya Michon, Anuradha F. Lingappa, Kumar Paulvannan et autres

3 citationsClinical Proteomics

Accès ouvert 2025 articleOpenAlex

Elucidating the Synergistic Effect of the PrimeC Combination for Amyotrophic Lateral Sclerosis in Human Induced Pluripotent Stem Cell-Derived Motor Neurons and Mouse Models

Shiran Salomon‐Zimri, Nitai Kerem, Gabriel Linares, Niva Russek‐Blum et autres

4 citationsPharmaceuticals

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