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Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes.

Modulation of crossbridge kinetics by myosin isoenzymes in skinned human heart fibers.

Dental chromatic alteration caused by neonatal cholestasis.

Morphological changes in liposomes caused by polymerization of encapsulated actin and spontaneous formation of actin bundles.

Effects of 2,3-butanedione monoxime on the crossbridge kinetics in frog single muscle fibres.

Defects in autophagy caused by glaucoma-associated mutations in optineurin.

Genetic alteration of proteins in actin-based motility systems.

Chronophin activation is necessary in Doxorubicin-induced actin cytoskeleton alteration.

Leber congenital amaurosis caused by mutations in GUCY2D.

X-linked Alport syndrome caused by splicing mutations in COL4A5.

The dynamics of actin and myosin association and the crossbridge model of muscle contraction.

Congenital myasthenic syndrome caused by mutations in DPAGT.

Diseases caused by mutations in ORAI1 and STIM1.

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Progressive microcephaly is caused by compound-heterozygous mutations in QARS.

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Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.

A human immunodeficiency caused by mutations in the PIK3R1 gene.

Kinetics of the cooperative association of actin to actin filaments.

Alteration in the neutral properties of Bio-Gel P caused by swelling in hot aqueous buffers.

Trichinella spiralis: alteration of gastrocnemius muscle kinetics in the mouse.

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Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes.

Modulation of crossbridge kinetics by myosin isoenzymes in skinned human heart fibers.

Dental chromatic alteration caused by neonatal cholestasis.

Morphological changes in liposomes caused by polymerization of encapsulated actin and spontaneous formation of actin bundles.

Effects of 2,3-butanedione monoxime on the crossbridge kinetics in frog single muscle fibres.

Defects in autophagy caused by glaucoma-associated mutations in optineurin.

Genetic alteration of proteins in actin-based motility systems.

Chronophin activation is necessary in Doxorubicin-induced actin cytoskeleton alteration.

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X-linked Alport syndrome caused by splicing mutations in COL4A5.

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A human immunodeficiency caused by mutations in the PIK3R1 gene.

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.

Progressive microcephaly is caused by compound-heterozygous mutations in QARS.

Similar phenotypes caused by mutations in OTOG and OTOGL.

Achromatopsia caused by novel missense mutations in the CNGA3 gene.

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Alteration in crossbridge kinetics caused by mutations in actin.

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