t/formins

Formins

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Recessive loss of DIAPH1 function causes a progressive neurodevelopmental syndrome with variable immunological involvement.
Formins
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Formins
Genetic associations of corneal astigmatism in Hong Kong Chinese children.
Formins
A large deletion spanning multiple enhancers near <i>PITX2</i> increases primary open-angle glaucoma risk
Formins
PhenoSS: Phenotype semantic similarity-based approach for rare disease prediction and patient clustering
Formins
Calcium directs actin assembly via allosteric activation of formin INF2
Formins
INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights.
Formins
Impact of N-terminal dimerization on formin homology 1 domain polymer dynamics and actin assembly
Formins
Autosomal dominant focal segmental glomerulosclerosis by INF2 p.Arg218Trp and p.Ser186Pro mutations: three case reports and literature review.
Formins
Regulation of the formin INF2 by actin monomers and calcium-calmodulin
Formins

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