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/vufind/Search/Results?lookfor=%22Shmukler%2C+Boris+E%22&type=Person&sort=year
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PubPharm (92)
1
The erythroid K-Cl cotransport inhibitor [(dihydroindenyl)oxy]acetic acid blocks erythroid Ca2+-activated K+ channel KCNN4
enthalten in:
American journal of physiology. Cell physiology
| 2022
von
Rivera, A.
|
Nasburg, J.
|
Shim, H.
| +8
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2
Erythroid-specific inactivation of Slc12a6/Kcc3 by EpoR promoter-driven Cre expression reduces K-Cl cotransport activity in mouse erythrocytes
enthalten in:
Physiological reports
| 2022
von
Shmukler, B.
|
Rivera, A.
|
Nishimura, K.
| +6
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3
Erythroid‐specific inactivation of Slc12a6/Kcc3 by EpoR promoter‐driven Cre expression reduces K‐Cl cotransport activity in mouse erythrocytes
enthalten in:
Physiological Reports
| 2022
von
Shmukler, B.
|
Rivera, A.
|
Nishimura, K.
| +6
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4
Trpv1 and Trpa1 are not essential for Psickle-like activity in red cells of the SAD mouse model of sickle cell disease
enthalten in:
Blood cells, molecules & diseases
| 2021
von
Vandorpe, D.
|
Rivera, A.
|
Shmukler, B.
| +6
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5
A Grammastola spatulata mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologies
enthalten in:
Haematologica
| 2021
von
Vandorpe, D.
|
Shmukler, B.
|
Ilboudo, Y.
| +11
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6
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis
enthalten in:
Kidney international
| 2020
von
Jobst-Schwan, T.
|
Klämbt, V.
|
Tarsio, M.
| +22
CommentIn: Kidney Int. 2020 Mar;97(3):452-455. - PMID 32087886
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7
Corrigendum to "Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease" [Blood Cells Mol. Dis. (2019) start page-end page not yet assigned] https://doi.org/10.1016/j.bcmd.2019.102346
enthalten in:
Blood cells, molecules & diseases
| 2020
von
Shmukler, B.
|
Rivera, A.
|
Bhargava, P.
| +8
ErratumFor: Blood Cells Mol Dis. 2019 Nov;79:102346. - PMID 31352162
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8
Genetic disruption of KCC cotransporters in a mouse model of thalassemia intermedia
enthalten in:
Blood cells, molecules & diseases
| 2020
von
Shmukler, B.
|
Rivera, A.
|
Bhargava, P.
| +11
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9
Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease
enthalten in:
Blood cells, molecules & diseases
| 2019
von
Shmukler, B.
|
Rivera, A.
|
Bhargava, P.
| +8
ErratumIn: Blood Cells Mol Dis. 2020 Mar;81:102390. - PMID 31931456
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10
Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells
enthalten in:
American journal of physiology. Cell physiology
| 2019
von
Rivera, A.
|
Vandorpe, D.
|
Shmukler, B.
| +11
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American journal of hematology
8
Blood cells, molecules & diseases
6
American journal of physiology. Cell physiology
6
Pflügers Archiv
5
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4
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4
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3
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Thema
41
Journal Article
35
Research Support, N.I.H., Extramural
35
Research Support, Non-U.S. Gov't
11
Chlorides
10
Chloride-Bicarbonate Antiporters
9
Symporters
8
Case Reports
8
Letter
7
Anion Exchange Protein 1, Erythrocyte
7
Antiporters
7
Intermediate-Conductance Calcium-Activated Pota...
6
Ion Channels
6
Potassium
6
RWP5GA015D
6
Sulfate Transporters
6
oocyte
5
Anion Transport Proteins
5
Bicarbonates
5
KCNN4 protein, human
5
Slc12a6 protein, mouse
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Erscheinungszeitraum
85
2000-
2
1900-1999
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Englisch
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