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/vufind/Search/Results?lookfor=%22Uapinyoying%2C+Prech%22&type=Person&sort=year
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PubPharm (25)
1
Differential inclusion of
NEB
exons 143 and 144 provides insight into
NEB
-related myopathy variant interpretation and disease manifestation
enthalten in:
bioRxiv.org
| 2024
von
Silverstein, S.
|
Orbach, R.
|
Syeda, S.
| +8
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2
Differential inclusion of NEB exons 143 and 144 provides insight into NEB-related myopathy variant interpretation and disease manifestation
enthalten in:
medRxiv : the preprint server for health sciences
| 2024
von
Silverstein, S.
|
Orbach, R.
|
Syeda, S.
| +8
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3
Allele-specific CRISPR/Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophy
enthalten in:
bioRxiv.org
| 2024
von
Bolduc, V.
|
Sizov, K.
|
Brull, A.
| +6
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4
Allele-specific CRISPR/Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophy
enthalten in:
bioRxiv : the preprint server for biology
| 2024
von
Bolduc, V.
|
Sizov, K.
|
Brull, A.
| +6
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5
Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic muscle
enthalten in:
iScience
| 2023
von
Uapinyoying, P.
|
Hogarth, M.
|
Battacharya, S.
| +4
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6
A recurrent homozygous missense DPM3 variant leads to muscle and brain disease
enthalten in:
Clinical genetics
| 2022
von
Nagy, S.
|
Lau, T.
|
Alavi, S.
| +16
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7
A new long-read RNA-seq analysis approach identifies and quantifies novel transcripts of very large genes
enthalten in:
bioRxiv.org
| 2022
von
Uapinyoying, P.
|
Goecks, J.
|
Knoblach, S.
| +5
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8
Impaired ureagenesis due to arginine-insensitive N-acetylglutamate synthase
enthalten in:
bioRxiv.org
| 2022
von
Sonaimuthu, P.
|
Senkevitch, E.
|
Haskins, N.
| +5
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9
Pathogenic role and therapeutic potential of fibro-adipogenic progenitors in muscle disease
enthalten in:
Trends in molecular medicine
| 2022
von
Hogarth, M.
|
Uapinyoying, P.
|
Mázala, D.
| +1
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10
A recurrent homozygous missense DPM3 variant leads to muscle and brain disease
sonderdruck aus:
Clinical genetics
| 2022
von
Nagy, S.
|
Lau, T.
|
Alavi, S.
| +16
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10
Research Support, N.I.H., Extramural
7
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4
570
4
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2
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2
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2
muscular dystrophy
1
31C4KY9ESH
1
77238-31-4
1
8L70Q75FXE
1
Acetates
1
Adaptor Proteins, Vesicular Transport
1
Adenosine Triphosphate
1
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1
BET1
1
CD11b Antigen
1
CRISPR/Cas9
1
Central Nervous System Agents
1
Chemokine CXCL10
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Erscheinungszeitraum
18
2020-
7
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
19
Englisch
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