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1.
Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss.
Ear Hear
; 44(6): 1464-1484, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37438890
2.
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.
Am J Hum Genet
; 105(3): 631-639, 2019 09 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31353024
3.
Diagnostic Yield of Targeted Hearing Loss Gene Panel Sequencing in a Large German Cohort With a Balanced Age Distribution from a Single Diagnostic Center: An Eight-year Study.
Ear Hear
; 43(3): 1049-1066, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-34753855
4.
Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression.
Hum Genet
; 139(2): 137-149, 2020 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-31786673
5.
Selective p38α MAP kinase/MAPK14 inhibition in enzymatically modified LDL-stimulated human monocytes: implications for atherosclerosis.
FASEB J
; 31(2): 674-686, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27871059
6.
Impact of p38 MAP Kinase Inhibitors on LPS-Induced Release of TNF-α in Whole Blood and Primary Cells from Different Species.
Cell Physiol Biochem
; 36(6): 2237-49, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26279429
7.
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.
Cell Rep
; 38(11): 110517, 2022 03 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35294868
8.
A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.
Front Genet
; 10: 7, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30766545
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