Query author contributions in Reactome

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Details on Person Mitchison, Hannah M

Class:Id	Person:9945666
_displayName	Mitchison, Hannah M
_timestamp	2025-04-16 19:18:14
created	[InstanceEdit:9945652] Rothfels, Karen, 2025-04-16
firstname	Hannah M
initial	HM
surname	Mitchison
(author)	[LiteratureReference:9945663] MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia [LiteratureReference:9960886] De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry [LiteratureReference:9967146] Axonemal structures reveal mechanoregulatory and disease mechanisms [LiteratureReference:9968797] CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms [LiteratureReference:9968814] DYX1C1 is required for axonemal dynein assembly and ciliary motility [LiteratureReference:9968835] HEATR2 plays a conserved role in assembly of the ciliary motile apparatus [LiteratureReference:9968905] Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia [LiteratureReference:9968914] Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia [LiteratureReference:9969764] X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 [LiteratureReference:9970758] DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport List all 12 refering instances
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No pathways have been reviewed or authored by Mitchison, Hannah M (9945666)