| A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant. | A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.
Morange PE, Peiretti F, Gourhant L, Proust C, Soukarieh O, Pulcrano-Nicolas AS, Saripella GV, Stefanucci L, Lacroix R, Ibrahim-Kosta M, Lemarié CA, Frontini M, Alessi MC, Trégouët DA, Couturaud F., Free PMC Article | 04/24/2021 |
| MAST1 variant causes mega-corpus-callosum syndrome with cortical malformations but without cerebellar hypoplasia. | MAST1 variant causes mega-corpus-callosum syndrome with cortical malformations but without cerebellar hypoplasia.
Rodríguez-García ME, Cotrina-Vinagre FJ, Gómez-Cano MLÁ, Martínez de Aragón A, Martín-Hernández E, Martínez-Azorín F. | 02/2/2021 |
| High MAST2 mRNA expression and its role in diagnosis and prognosis of liver cancer. | High MAST2 mRNA expression and its role in diagnosis and prognosis of liver cancer.
Jiao Y, Li Y, Jiang P, Fu Z, Liu Y., Free PMC Article | 11/21/2020 |
| we observed 3 case-specific duplications of the autosomal gene MAST2, and in a replication phase we found another 11 duplications | A Screen for Genomic Disorders of Infertility Identifies MAST2 Duplications Associated with Nonobstructive Azoospermia in Humans.
Huang N, Wen Y, Guo X, Li Z, Dai J, Ni B, Yu J, Lin Y, Zhou W, Yao B, Jiang Y, Sha J, Conrad DF, Hu Z., Free PMC Article | 06/28/2016 |
| Viral and PTEN peptide interactions to MAST2-PDZ occur via a unique kinetic step which involves both canonical C-terminal PBM binding and N-terminal anchoring. | Deciphering the unconventional peptide binding to the PDZ domain of MAST2.
Delhommel F, Chaffotte A, Terrien E, Raynal B, Buc H, Delepierre M, Cordier F, Wolff N. | 09/26/2015 |
| MAST2 gene rearrangements occur in invasive breast carcinoma. | MAST2 and NOTCH1 translocations in breast carcinoma and associated pre-invasive lesions.
Clay MR, Varma S, West RB. | 01/25/2014 |
| MAST205 plays an important role in regulating CFTR expression and function | MAST205 competes with cystic fibrosis transmembrane conductance regulator (CFTR)-associated ligand for binding to CFTR to regulate CFTR-mediated fluid transport.
Ren A, Zhang W, Yarlagadda S, Sinha C, Arora K, Moon CS, Naren AP., Free PMC Article | 06/29/2013 |
| The MAST2 sequence at the 5' end of SVA(F1) acts as a positive transcriptional regulator in human germ cells. | Transcriptional regulation of human-specific SVAF₁ retrotransposons by cis-regulatory MAST2 sequences.
Zabolotneva AA, Bantysh O, Suntsova MV, Efimova N, Malakhova GV, Schumann GG, Gayfullin NM, Buzdin AA. | 09/29/2012 |
| Overexpression of MAST1 or MAST2 gene fusions has a proliferative effect both in vitro and in vivo in breast cancer cell lines. | Functionally recurrent rearrangements of the MAST kinase and Notch gene families in breast cancer.
Robinson DR, Kalyana-Sundaram S, Wu YM, Shankar S, Cao X, Ateeq B, Asangani IA, Iyer M, Maher CA, Grasso CS, Lonigro RJ, Quist M, Siddiqui J, Mehra R, Jing X, Giordano TJ, Sabel MS, Kleer CG, Palanisamy N, Natrajan R, Lambros MB, Reis-Filho JS, Kumar-Sinha C, Chinnaiyan AM., Free PMC Article | 02/4/2012 |
| Recruitment of a MAST2 CpG island was most likely beneficial to the hybrid retrotransposons because it could significantly increase retrotransposition frequency. | Novel family of human transposable elements formed due to fusion of the first exon of gene MAST2 with retrotransposon SVA.
Bantysh OB, Buzdin AA. | 03/22/2010 |
| Studies report the identification of a new subfamily of SVA, which apparently formed after an alternative splicing event where the first exon of the MAST2 gene spliced into an intronic SVA and subsequently retrotransposed. | Exon-trapping mediated by the human retrotransposon SVA.
Hancks DC, Ewing AD, Chen JE, Tokunaga K, Kazazian HH Jr., Free PMC Article | 01/21/2010 |