Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension. (Q34361662)

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6 March 2020

title

Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension (English)

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Elena A B Azizan

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language of work or name

English

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publication date

4 August 2013

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6 March 2020

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volume

45

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page(s)

1055-1060

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issue

9

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https://scigraph.springernature.com/pub.10.1038/ng.2716

6 March 2020

exact match

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cites work

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Primary aldosteronism with aldosterone-producing adenoma consisting of pure zona glomerulosa-type cells in a pregnant woman

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Differential regulation of apoptosis in the normal human adrenal gland

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alpha 1D (Cav1.3) subunits can form l-type Ca2+ channels activating at negative voltages

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Evaluation of the sensitivity and specificity of (11)C-metomidate positron emission tomography (PET)-CT for lateralizing aldosterone secretion by Conn's adenomas.

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Inhibition of Aldosterone Secretion by Ouabain in Dog Adrenal Cortical Tissue

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A third Na+-binding site in the sodium pump

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Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

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12 December 2020

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.

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Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

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Effect of extracellular pH on presteady-state and steady-state current mediated by the Na+/K+ pump

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Calcium-channel blockade can mask the diagnosis of Conn's syndrome

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Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels

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C-terminal modulator controls Ca2+-dependent gating of Ca(v)1.4 L-type Ca2+ channels

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Ghrelin enhances the growth of cultured human adrenal zona glomerulosa cells by exerting MAPK-mediated proliferogenic and antiapoptotic effects

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Microarray, qPCR, and KCNJ5 sequencing of aldosterone-producing adenomas reveal differences in genotype and phenotype between zona glomerulosa- and zona fasciculata-like tumors

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A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients

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Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

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Crystal structures of the calcium pump and sarcolipin in the Mg2+-bound E1 state

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The sarcolipin-bound calcium pump stabilizes calcium sites exposed to the cytoplasm

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