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1.
AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia.
Am J Hum Genet
; 110(9): 1470-1481, 2023 09 07.
Article
in English
| MEDLINE | ID: mdl-37582359
2.
CHARGE syndrome and related disorders: a mechanistic link.
Hum Mol Genet
; 30(23): 2215-2224, 2021 11 16.
Article
in English
| MEDLINE | ID: mdl-34230955
3.
USP22 promotes HER2-driven mammary carcinoma aggressiveness by suppressing the unfolded protein response.
Oncogene
; 40(23): 4004-4018, 2021 06.
Article
in English
| MEDLINE | ID: mdl-34007022
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