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/vufind/Search/Results?lookfor=%22Spontarelli%2C+Kerri%22&type=Person&sort=year
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PubPharm (13)
1
ATP1A1
-linked diseases require a malfunctioning protein product from one allele
enthalten in:
bioRxiv.org
| 2024
von
Spontarelli, K.
|
Young, V.
|
Sweazey, R.
| +14
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2
ATP1A1-linked diseases require a malfunctioning protein product from one allele
enthalten in:
Biochimica et biophysica acta. Molecular cell research
| 2024
von
Spontarelli, K.
|
Young, V.
|
Sweazey, R.
| +14
UpdateOf: bioRxiv. 2023 Mar 05;:. - PMID 37090550
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3
A Na pump with reduced stoichiometry is up-regulated by brine shrimp in extreme salinities
enthalten in:
Proceedings of the National Academy of Sciences of the United States of America
| 2023
von
Artigas, P.
|
Meyer, D.
|
Young, V.
| +9
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4
The phenotypic spectrum of pathogenic ATP1A1 variants expands : the novel p.P600R substitution causes demyelinating Charcot-Marie-Tooth disease
enthalten in:
Journal of neurology
| 2023
von
Cinarli Yuksel, F.
|
Nicolaou, P.
|
Spontarelli, K.
| +8
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5
ATP1A1 -linked diseases require a malfunctioning protein product from one allele
enthalten in:
bioRxiv : the preprint server for biology
| 2023
von
Spontarelli, K.
|
Young, V.
|
Sweazey, R.
| +14
UpdateIn: Biochim Biophys Acta Mol Cell Res. 2023 Sep 1;1871(1):119572. - PMID 37659504
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6
The phenotypic spectrum of pathogenic ATP1A1 variants expands: the novel p.P600R substitution causes demyelinating Charcot–Marie–Tooth disease
enthalten in:
Journal of neurology
| 2023
von
Cinarli Yuksel, F.
|
Nicolaou, P.
|
Spontarelli, K.
| +8
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7
The phenotypic spectrum of pathogenic ATP1A1 variants expands: the novel p.P600R substitution causes demyelinating Charcot–Marie–Tooth disease
enthalten in:
Journal of neurology
| 2023
von
Cinarli Yuksel, F.
|
Nicolaou, P.
|
Spontarelli, K.
| +8
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8
The phenotypic spectrum of pathogenic ATP1A1 variants expands: the novel p.P600R substitution causes demyelinating Charcot–Marie–Tooth disease
enthalten in:
Journal of neurology
| 2023
von
Cinarli Yuksel, F.
|
Nicolaou, P.
|
Spontarelli, K.
| +8
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9
Role of a conserved ion-binding site tyrosine in ion selectivity of the Na+/K+ pump
enthalten in:
The Journal of general physiology
| 2022
von
Spontarelli, K.
|
Infield, D.
|
Nielsen, H.
| +6
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10
Diseases caused by mutations in the Na+/K+ pump α1 gene ATP1A1
enthalten in:
American journal of physiology. Cell physiology
| 2021
von
Biondo, E.
|
Spontarelli, K.
|
Ababioh, G.
| +2
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1
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13
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Journal of neurology
2
The Journal of general physiology
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Thema
7
EC 7.2.2.13
7
Journal Article
7
Sodium-Potassium-Exchanging ATPase
5
9NEZ333N27
5
ATP1A1
5
Sodium
4
Charcot–Marie–Tooth
4
Electrophysiology
4
Expression
4
Ouabain survival assay
3
/K
3
ATP1A1 protein, human
3
ATPase
3
EC 3.6.1.-
3
Na
3
Research Support, N.I.H., Extramural
3
Research Support, Non-U.S. Gov't
3
Research Support, U.S. Gov't, Non-P.H.S.
2
Ions
2
Potassium
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Erscheinungszeitraum
11
2020-
2
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
13
Englisch
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