# Late Breaking News

PMC · DOI: 10.1111/ene.70263 · European Journal of Neurology · 2025-06-21

## Full-text entities

- **Genes:** TARDBP (TAR DNA binding protein) [NCBI Gene 23435] {aka ALS10, TDP-43}, SPRED1 (sprouty related EVH1 domain containing 1) [NCBI Gene 161742] {aka LGSS, NFLS, PPP1R147, hSpred1, spred-1}, FCGRT (Fc gamma receptor and transporter) [NCBI Gene 2217] {aka FCRN, FcgammaRn, alpha-chain}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, SAA [NCBI Gene 6287], GRN (granulin precursor) [NCBI Gene 2896] {aka CLN11, FTD2, GEP, GP88, PCDGF, PEPI}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, C9orf72 (C9orf72-SMCR8 complex subunit) [NCBI Gene 203228] {aka ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1}
- **Diseases:** Dementias (MESH:D003704), hypersensitivity (MESH:D004342), neuro-axonal degeneration (MESH:D009410), Generalised myasthenia gravis (MESH:D009157), ALS (MESH:D008113), disability (MESH:D009069), Migraine (MESH:D008881), NMOSD (MESH:D009471), PPTH (MESH:D051298), FTD (MESH:D057180), Photophobia (MESH:D020795), MOGAD (MESH:D003711), Amyotrophic Lateral Sclerosis (MESH:D000690), toxicity (MESH:D064420), autoimmune disorder (MESH:D001327), PD (MESH:D010300), autoimmune antibody mediated diseases (MESH:D020274), Pain (MESH:D010146), PPR (OMIM:132100), Myasthenia (MESH:D020294), Neurodegenerative Disorders (MESH:D019636), Cephalalgia (MESH:D006261), synucleinopathy (MESH:D000080874), Neuroinflammatory Dysfunction (MESH:D000090862), headache disorders (MESH:D020773), muscle weakness (MESH:D018908), Alzheimer (MESH:D000544)
- **Chemicals:** C5IT (-), Efgartigimod (MESH:C000718373), ravulizumab (MESH:C000629409), methylprednisolone (MESH:D008775), oxygen (MESH:D010100), eculizumab (MESH:C481642)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** A53T
- **Cell lines:** LBN_03 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_C6NK), 01 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_A1PP), LBN_02 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_VU41), 04 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_S856), LBN_06 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_S857)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12181676/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12181676/full.md

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Source: https://tomesphere.com/paper/PMC12181676