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/vufind/Search/Results?lookfor=%22Muhammad%2C+Ayesha%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Muhammad%2C+Ayesha%22&type=Person&sort=year
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PubPharm (22)
1
Emergency trauma care : Pakistan's preparedness amidst the growing impact of rapid climate change
enthalten in:
International journal of surgery (London, England)
| 2024
von
Muhammad, A.
|
Qureshi, A.
|
Farhan, M.
| +3
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2
Multifocal Ectopic Purkinje Premature Contractions due to neutralization of an
SCN5A
negative charge: structural insights into the gating pore hypothesis
enthalten in:
bioRxiv.org
| 2024
von
Glazer, A.
|
Yang, T.
|
Li, B.
| +11
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3
Multifocal Ectopic Purkinje Premature Contractions due to neutralization of an SCN5A negative charge : structural insights into the gating pore hypothesis
enthalten in:
bioRxiv : the preprint server for biology
| 2024
von
Glazer, A.
|
Yang, T.
|
Li, B.
| +11
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4
Multi-site validation of a functional assay to adjudicate
SCN5A
Brugada Syndrome-associated variants
enthalten in:
bioRxiv.org
| 2023
von
Ma, J.
|
O’Neill, M.
|
Richardson, E.
| +17
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5
Multi-site validation of a functional assay to adjudicate SCN5A Brugada Syndrome-associated variants
enthalten in:
medRxiv : the preprint server for health sciences
| 2023
von
Ma, J.
|
O'Neill, M.
|
Richardson, E.
| +17
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6
High-throughput reclassification of
SCN5A
variants
enthalten in:
bioRxiv.org
| 2023
von
Glazer, A.
|
Wada, Y.
|
Li, B.
| +10
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7
Variant-based heritability assessment of dexmedetomidine and fentanyl clearance in pediatric patients
enthalten in:
Clinical and translational science
| 2023
von
Shannon, M.
|
Muhammad, A.
|
James, N.
| +7
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8
High-throughput functional mapping of variants in an arrhythmia gene,
KCNE1
, reveals novel biology
enthalten in:
bioRxiv.org
| 2023
von
Muhammad, A.
|
Calandranis, M.
|
Li, B.
| +10
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9
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology
enthalten in:
bioRxiv : the preprint server for biology
| 2023
von
Muhammad, A.
|
Calandranis, M.
|
Li, B.
| +10
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10
Dominant negative effects of
SCN5A
missense variants
enthalten in:
bioRxiv.org
| 2023
von
O’Neill, M.
|
Muhammad, A.
|
Li, B.
| +6
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10
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8
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8
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6
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6
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3
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2
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2
NAV1.5 Voltage-Gated Sodium Channel
2
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2
SCN5A protein, human
2
long QT syndrome
1
67VB76HONO
1
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1
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1
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1
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1
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1
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1
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1
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Erscheinungszeitraum
18
2020-
4
2010-2019
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Sprache
20
Englisch
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