Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome.

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Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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Homozygous deletion in MYL9 ex ...... inal hypoperistalsis syndrome.

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Homozygous deletion in MYL9 ex ...... inal hypoperistalsis syndrome.

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Homozygous deletion in MYL9 ex ...... inal hypoperistalsis syndrome.

@en

Homozygous deletion in MYL9 ex ...... inal hypoperistalsis syndrome.

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Homozygous deletion in MYL9 ex ...... inal hypoperistalsis syndrome.

@en

Homozygous deletion in MYL9 ex ...... inal hypoperistalsis syndrome.

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P1476

Homozygous deletion in MYL9 ex ...... tinal hypoperistalsis syndrome

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P2093

Carolina Araujo Moreno

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Denise Pontes Cavalcanti

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Elizabeth Pugh

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Gary Steel

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Nara Sobreira

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Peng Zhang

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P2860

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

Characterization and differential expression of human vascular smooth muscle myosin light chain 2 isoform in nonmuscle cells

Mutations in myosin light chain kinase cause familial aortic dissections

Junb regulates arterial contraction capacity, cellular contractility, and motility via its target Myl9 in mice

Smooth-muscle contraction without smooth-muscle myosin

Smooth muscle contraction and relaxation

The molecular anatomy of caldesmon

Identification, phosphorylation, and dephosphorylation of a second site for myosin light chain kinase on the 20,000-dalton light chain of smooth muscle myosin

Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice.

Autonomic control of the eye.

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s41431-017-0055-5

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669-675

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scholarly article

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10.1038/S41431-017-0055-5

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P433

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P478

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Fábio Rossi Torres

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2018-02-16T00:00:00Z

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29453416

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5945668

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