Cargando…
Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome
INTRODUCTION: Most of the approximately 60 genes that if mutated cause steroid-resistant nephrotic syndrome (SRNS) are highly expressed in the glomerular podocyte, rendering SRNS a “podocytopathy.” METHODS: We performed whole-exome sequencing (WES) in 1200 nephrotic syndrome (NS) patients. RESULTS:...
Autores principales: | Mao, Youying, Schneider, Ronen, van der Ven, Peter F.M., Assent, Marvin, Lohanadan, Keerthika, Klämbt, Verena, Buerger, Florian, Kitzler, Thomas M., Deutsch, Konstantin, Nakayama, Makiko, Majmundar, Amar J., Mann, Nina, Hermle, Tobias, Onuchic-Whitford, Ana C., Zhou, Wei, Margam, Nandini Nagarajan, Duncan, Roy, Marquez, Jonathan, Khokha, Mustafa, Fathy, Hanan M., Kari, Jameela A., El Desoky, Sherif, Eid, Loai A., Awad, Hazem Subhi, Al-Saffar, Muna, Mane, Shrikant, Lifton, Richard P., Fürst, Dieter O., Shril, Shirlee, Hildebrandt, Friedhelm |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879128/ https://www.ncbi.nlm.nih.gov/pubmed/33615072 http://dx.doi.org/10.1016/j.ekir.2020.10.040 |
Ejemplares similares
-
Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches
por: Klämbt, Verena, et al.
Publicado: (2020) -
SYNPO2 upregulation is an unfavorable prognostic factor for nasopharyngeal carcinoma patients
por: Chang, Shih-Lun, et al.
Publicado: (2023) -
Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation
por: Clausen, Alexander Guldmann, et al.
Publicado: (2021) -
Autism-related KLHL17 and SYNPO act in concert to control activity-dependent dendritic spine enlargement and the spine apparatus
por: Hu, Hsiao-Tang, et al.
Publicado: (2023) -
SynPo-Net—Accurate and Fast CNN-Based 6DoF Object Pose Estimation Using Synthetic Training
por: Su, Yongzhi, et al.
Publicado: (2021)