Norepinephrine deficiency is caused by combined abnormal mRNA processing and defective protein trafficking of dopamine beta-hydroxylase (Q34685511)

3 August 2017

title

Norepinephrine deficiency is caused by combined abnormal mRNA processing and defective protein trafficking of dopamine beta-hydroxylase (English)

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3 August 2017

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7

Hoon Ryu

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3 August 2017

Chun-Hyung Kim

1

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3 August 2017

Amanda Leung

2

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3 August 2017

Yang Hoon Huh

3

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3 August 2017

Eungi Yang

4

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3 August 2017

Deog-Joong Kim

5

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3 August 2017

Pierre Leblanc

6

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3 August 2017

Kyungjin Kim

8

1 reference

3 August 2017

Dong-Wook Kim

9

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3 August 2017

Emily M Garland

10

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3 August 2017

Satish R Raj

11

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3 August 2017

Italo Biaggioni

12

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3 August 2017

David Robertson

13

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3 August 2017

Kwang-Soo Kim

14

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3 August 2017

language of work or name

English

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publication date

5 January 2011

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Journal of Biological Chemistry

3 August 2017

published in

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3 August 2017

volume

286

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3 August 2017

issue

11

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3 August 2017

page(s)

9196-9204

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L-Dihydroxyphenylserine (L-DOPS): a norepinephrine prodrug

3 August 2017

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7 July 2018

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7 July 2018

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7 July 2018

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Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development

7 July 2018

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Proportional Release of Norepinephrine and Dopamine-β-Hydroxylase from Sympathetic Nerves

7 July 2018

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Photometric assay of dopamine- -hydroxylase activity in human blood.

7 July 2018

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7 July 2018

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Dopamine beta-hydroxylase of adrenal chromaffin granules: structure and function

7 July 2018

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Isolated failure of autonomic noradrenergic neurotransmission. Evidence for impaired beta-hydroxylation of dopamine

7 July 2018

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7 July 2018

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Clinical, autonomic and therapeutic observations in two siblings with postural hypotension and sympathetic failure due to an inability to synthesize noradrenaline from dopamine because of a deficiency of dopamine beta hydroxylase.

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Dopamine beta-hydroxylase immunoreactivity in human cerebrospinal fluid: properties, relationship to central noradrenergic neuronal activity and variation in Parkinson's disease and congenital dopamine beta-hydroxylase deficiency

7 July 2018

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Crossref

https://api.crossref.org/works/10.1074%2FJBC.M110.192351

Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiency

21 January 2018

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26 October 2018

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21 January 2018

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Cell type-specific storage of dopamine beta-monooxygenase

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21209083

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The ER function BiP is a master regulator of ER function

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21209083

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1074/JBC.M110.192351

1 reference

3 August 2017

1 reference

3 August 2017

1 reference