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PubPharm (66)
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
Na+,K+-ATPase with Disrupted Na+ Binding Sites I and III Binds Na+ with Increased Affinity at Site II and Undergoes Na+-Activated Phosphorylation with ATP
enthalten in:
Biomolecules
| 2024
von
Nielsen, H.
|
Holm, R.
|
Sweazey, R.
| +3
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3
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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4
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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5
An unusual conformation from Na+-sensitive non-gastric proton pump mutants reveals molecular mechanisms of cooperative Na+-binding
enthalten in:
Biochimica et biophysica acta. Molecular cell research
| 2023
von
Abe, K.
|
Nishizawa, T.
|
Artigas, P.
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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
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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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
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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10
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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Thema
34
Journal Article
30
EC 7.2.2.13
30
Sodium-Potassium-Exchanging ATPase
20
Research Support, N.I.H., Extramural
18
9NEZ333N27
18
Sodium
17
Research Support, Non-U.S. Gov't
12
Potassium
12
RWP5GA015D
10
Research Support, U.S. Gov't, Non-P.H.S.
6
5ACL011P69
6
Acrylamides
6
Cnidarian Venoms
6
EC 3.6.1.-
6
Ions
6
OQ17NC0MOV
6
Ouabain
6
palytoxin
5
8L70Q75FXE
5
ATP1A1
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Erscheinungszeitraum
15
2020-
30
2010-2019
19
2000-2009
Erscheinungsjahr(e)
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Sprache
47
Englisch
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