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Lone, Museer A.
51
results:
Search for persons
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Online (51)
Mediatypes
Articles (Online) (21)
Bookchapter (Online) (1)
OpenAccess-fulltext (29)
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1
CERT1 mutations perturb human development by disrupting sph..:
Gehin, Charlotte
;
Lone, Museer A.
;
Lee, Winston
...
Journal of Clinical Investigation. 133 (2023) 10 - p. , 2023
Link:
https://doi.org/10.1172/..
?
2
Editorial: Genetic disorders and rare diseases: in vitro mo..:
Hassan, Shabir
;
Lone, Museer A.
Frontiers in Pharmacology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Recurrent de novoSPTLC2variant causes childhood-onset amyot..:
Syeda, Safoora B
;
Lone, Museer A
;
Mohassel, Payam
...
Journal of Neurology, Neurosurgery & Psychiatry. 95 (2023) 2 - p. 103-113 , 2023
Link:
https://doi.org/10.1136/..
?
4
SPTLC1 p.Leu38Arg, a novel mutation associated with childho..:
Lone, Museer A.
;
Zeng, Sen
;
Bourquin, Florence
...
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1868 (2023) 9 - p. 159359 , 2023
Link:
https://doi.org/10.1016/..
?
5
CERT1 mutations perturb human development by disrupting sph..:
Gehin, Charlotte
;
Lone, Museer A
;
Lee, Winston
...
https://doi.org/10.1172/JCI165019. , 2023
Link:
https://hdl.handle.net/2..
?
6
CERT1 mutations perturb human development by disrupting sph..:
Gehin, Charlotte
;
Lone, Museer
;
Lee, Winston
...
The Journal of Clinical Investigation;133(10). , 2023
Link:
https://hdl.handle.net/1..
?
7
CERT1 mutations perturb human development by disrupting sph..:
Gehin, Charlotte
;
Lone, Museer A
;
Lee, Winston
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178846/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
8
Editorial: Genetic disorders and rare diseases: in vitro mo..:
Shabir Hassan
;
Museer A. Lone
https://www.frontiersin.org/articles/10.3389/fphar.2023.1346648/full. , 2023
Link:
https://doi.org/10.3389/..
?
9
Recurrent de novo SPTLC2 variant causes childhood-onset amy..:
Syeda, Safoora B
;
Lone, Museer A
;
Mohassel, Payam
...
https://discovery.ucl.ac.uk/id/eprint/10183851/1/jnnp-2023-332132.full.pdf. , 2023
Link:
https://discovery.ucl.ac..
?
10
CERT1 mutations perturb human development by disrupting sph..:
Charlotte Gehin
;
Museer A. Lone
;
Winston Lee
...
https://doi.org/10.1172/JCI165019. , 2023
Link:
https://doaj.org/article..
?
11
CERT1 mutations perturb human development by disrupting sph..:
Gehin, Charlotte
;
Lone, Museer A
;
Lee, Winston
...
https://boris.unibe.ch/189663/. , 2023
Link:
https://boris.unibe.ch/1..
?
12
CERT1 mutations perturb human development by disrupting sph..:
Gehin, Charlotte
;
Lone, Museer A
;
Lee, Winston
...
info:eu-repo/semantics/altIdentifier/pmid/36976648. , 2023
Link:
https://hdl.handle.net/1..
?
13
Serine Palmitoyltransferase Subunit 3 and Metabolic Disease:
, In:
Sphingolipid Metabolism and Metabolic Disease; Advances in Experimental Medicine and Biology
,
Lone, Museer A.
;
Bourquin, Florence
;
Hornemann, Thorsten
- p. 47-56 , 2022
Link:
https://doi.org/10.1007/..
?
14
SPTLC1 variants associated with ALS produce distinct sphing..:
Lone, Museer A.
;
Aaltonen, Mari J.
;
Zidell, Aliza
...
Journal of Clinical Investigation. 132 (2022) 18 - p. , 2022
Link:
https://doi.org/10.1172/..
?
15
Precision Mouse Models of Yars/Dominant Intermediate Charco..:
Hines, Timothy J
;
Tadenev, Abigail L. D
;
Lone, Museer A
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170831/. , 2022
Link:
http://www.ncbi.nlm.nih...
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