Cargando…
Deleting the mouse Hsd17b1 gene results in a hypomorphic Naglu allele and a phenotype mimicking a lysosomal storage disease
HSD17B1 is a steroid metabolising enzyme. We have previously generated knockout mice that had the entire coding region of Hsd17b1 replaced with lacZ-neo cassette (Hsd17b1-LacZ/Neo mice). This resulted in a 90% reduction of HSD17B1 activity, associated with severe subfertility in the knockout females...
Autores principales: | Jokela, Heli, Hakkarainen, Janne, Kätkänaho, Laura, Pakarinen, Pirjo, Ruohonen, Suvi T., Tena-Sempere, Manuel, Zhang, Fu-Ping, Poutanen, Matti |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703720/ https://www.ncbi.nlm.nih.gov/pubmed/29180785 http://dx.doi.org/10.1038/s41598-017-16618-5 |
Ejemplares similares
-
EGFR activation triggers cellular hypertrophy and lysosomal disease in NAGLU-depleted cardiomyoblasts, mimicking the hallmarks of mucopolysaccharidosis IIIB
por: De Pasquale, Valeria, et al.
Publicado: (2018) -
Differential Uptake of NAGLU-IGF2 and Unmodified NAGLU in Cellular Models of Sanfilippo Syndrome Type B
por: Prill, Heather, et al.
Publicado: (2019) -
Downregulation of NAGLU in VEC Increases Abnormal Accumulation of Lysosomes and Represents a Predictive Biomarker in Early Atherosclerosis
por: Xing, Changchang, et al.
Publicado: (2022) -
THU574 Hsd17b1 Partially Compensates For The Lack Of Hsd17b3 In Testicular Testosterone Production In Fetal Mice, But Not In Adults
por: Poutanen, Matti, et al.
Publicado: (2023) -
Brdm2 – an aberrant hypomorphic p63 allele
por: Talos, Flaminia, et al.
Publicado: (2010)