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1.
Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16.
Int J Mol Sci
; 22(11)2021 May 30.
Article
in English
| MEDLINE | ID: mdl-34070858
2.
Disease-stabilizing treatment based on all-trans retinoic acid and valproic acid in acute myeloid leukemia - identification of responders by gene expression profiling of pretreatment leukemic cells.
BMC Cancer
; 17(1): 630, 2017 Sep 06.
Article
in English
| MEDLINE | ID: mdl-28877686
3.
In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins.
Biosci Rep
; 37(2)2017 04 30.
Article
in English
| MEDLINE | ID: mdl-28396517
4.
Nucleosome binding by the bromodomain and PHD finger of the transcriptional cofactor p300.
J Mol Biol
; 337(4): 773-88, 2004 Apr 02.
Article
in English
| MEDLINE | ID: mdl-15033350
5.
STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity.
Orphanet J Rare Dis
; 9: 146, 2014 Sep 26.
Article
in English
| MEDLINE | ID: mdl-25258038
6.
The Arabidopsis SET-domain protein ASHR3 is involved in stamen development and interacts with the bHLH transcription factor ABORTED MICROSPORES (AMS).
Plant Mol Biol
; 66(1-2): 47-59, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-17978851
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