Cargando…
Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency
In this study, we performed a genome-wide N-ethyl-N-nitrosourea (ENU) mutagenesis screen in mice to identify novel genes or alleles that regulate erythropoiesis. Here, we describe a recessive mouse strain, called RBC19, harbouring a point mutation within the housekeeping gene, Tpi1, which encodes th...
Autores principales: | Conway, Ashlee J., Brown, Fiona C., Hortle, Elinor J., Burgio, Gaetan, Foote, Simon J., Morton, Craig J., Jane, Stephen M., Curtis, David J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992613/ https://www.ncbi.nlm.nih.gov/pubmed/29720471 http://dx.doi.org/10.1242/dmm.034678 |
Ejemplares similares
-
A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
por: Conway, Ashlee J., et al.
Publicado: (2017) -
Hæmolytic Anæmias
por: Davis, L. J.
Publicado: (1943) -
KCC1 Activation protects Mice from the Development of Experimental Cerebral Malaria
por: Hortle, Elinor, et al.
Publicado: (2019) -
Author Correction: KCC1 Activation protects Mice from the Development of Experimental Cerebral Malaria
por: Hortle, Elinor, et al.
Publicado: (2020) -
Hæmolytic Anæmia
por: Chhuttani, P. N.
Publicado: (1943)