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Forst, Anna-Lena
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1

EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- an..:

Lo, Jacky ; Forst, Anna-Lena ; Warth, Richard.
Frontiers in Physiology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

Genetic variants in eleven central and peripheral chemorece..:

Neubauer, Jacqueline ; Forst, Anna-Lena ; Warth, Richard...
Pediatric Research.  92 (2022)  4 - p. 1026-1033 , 2022
Link: https://doi.org/10.1038/..
 
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3

Distinct Mitochondrial Pathologies Caused by Mutations of t..:

Forst, Anna-Lena ; Reichold, Markus ; Kleta, Robert.
Frontiers in Physiology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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4

Novel mutations in the KCNJ10 gene associated to a distinct..:

Morin, Matias ; Forst, Anna-Lena ; Pérez-Torre, Paula...
neurogenetics.  21 (2020)  2 - p. 135-143 , 2020
Link: https://doi.org/10.1007/..
 
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5

Dynamic NHERF interaction with TRPC4/5 proteins is required..:

Storch, Ursula ; Forst, Anna-Lena ; Pardatscher, Franziska...
Proceedings of the National Academy of Sciences of the United States of America.  114 (2017)  1 - p. E37-E46 , 2017
Link: https://www.jstor.org/st..
 
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6

Dynamic NHERF interaction with TRPC4/5 proteins is required..:

Storch, Ursula ; Forst, Anna-Lena ; Pardatscher, Franziska...
Proceedings of the National Academy of Sciences.  114 (2016)  1 - p. , 2016
Link: https://doi.org/10.1073/..
 
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7

Novel role of mechanosensitive AT1B receptors in myogenic v..:

Blodow, Stephanie ; Schneider, Holger ; Storch, Ursula...
Pflügers Archiv - European Journal of Physiology.  466 (2013)  7 - p. 1343-1353 , 2013
Link: https://doi.org/10.1007/..
 
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8

Transient Receptor Potential Channel 1 (TRPC1) Reduces Calc..:

Storch, Ursula ; Forst, Anna-Lena ; Philipp, Maximilian..
Journal of Biological Chemistry.  287 (2012)  5 - p. 3530-3540 , 2012
Link: https://doi.org/10.1074/..
 
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9

Enzymatic disease of the podocyte:

Kistler, Andreas D. ; Peev, Vasil ; Forst, Anna-Lena...
Pediatric Nephrology.  25 (2010)  6 - p. 1017-1023 , 2010
Link: https://doi.org/10.1007/..
 
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10

Functional Analysis of the Kv1.1 N255D Mutation Associated ..:

van der Wijst, Jenny ; Glaudemans, Bob ; Venselaar, Hanka...
Journal of Biological Chemistry.  285 (2010)  1 - p. 171-178 , 2010
Link: https://doi.org/10.1074/..
 
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11

Genetic variants in eleven central and peripheral chemorece..:

Neubauer, Jacqueline ; Forst, Anna-Lena ; Warth, Richard...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586864/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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12

A Founder Mutation in EHD1 Presents with Tubular Proteinuri..:

Issler, Naomi ; Afonso, Sara ; Weissman, Irith...
https://discovery.ucl.ac.uk/id/eprint/10147913/1/EHD1-manuscript-2021-12-16fn.pdf.  , 2022
Link: https://discovery.ucl.ac..
 
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13

EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- an..:

Lo, Jacky ; Forst, Anna-Lena ; Warth, Richard.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965613/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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14

Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemi..:

Schlingmann, Karl P ; Renigunta, Aparna ; Hoorn, Ewout J...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259640/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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15

Distinct Mitochondrial Pathologies Caused by Mutations of t..:

Forst, Anna-Lena ; Reichold, Markus ; Kleta, Robert.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326905/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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