Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy.

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Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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label

Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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P1476

Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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Basar Candemir

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Erhan Saracoglu

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Ertan Vuruskan

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Fatih Poyraz

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Fethi Yavuz

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Hüseyin Göksülük

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Irfan V Düzen

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Seniz Demiryürek

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Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

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PI(3,5)P2 controls membrane trafficking by direct activation of mucolipin Ca2+ release channels in the endolysosome

Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins

Whole blood gene expression and atrial fibrillation: the Framingham Heart Study.

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s41598-017-10039-0

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scholarly article

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10.1038/S41598-017-10039-0

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English

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2017-08-24T00:00:00Z

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1091273030

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28839241

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5571177

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Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

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P2860

P2860

Leukocyte TRP channel gene expressions in patients with non-valvular atrial fibrillation

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P577

P6179

P698

P932