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1.
Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytes.
Basic Res Cardiol
; 119(1): 151-168, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38145999
2.
Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome.
Am J Hum Genet
; 102(4): 696-705, 2018 04 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29606302
3.
CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants.
Cell Genom
; 2(2)2022 Feb 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35252945
4.
High-Throughput Analysis of the Cell and DNA Site-Specific Binding of Native NF-κB Dimers Using Nuclear Extract Protein-Binding Microarrays (NextPBMs).
Methods Mol Biol
; 2366: 43-66, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34236632
5.
Decision-Making and Relationship Competence When Reporting Suspected Physical Abuse and Child Neglect: An Objective Structured Clinical Evaluation.
Clin Soc Work J
; 49(2): 256-270, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33583967
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