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Page 1
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.
Dhekne HS, Pylypenko O, Overeem AW, Zibouche M, Ferreira RJ, van der Velde KJ, Rings EHHM, Posovszky C, van der Sluijs P, Swertz MA, Houdusse A, van IJzendoorn SCD. Dhekne HS, et al. Among authors: overeem aw. Hum Mutat. 2018 Mar;39(3):333-344. doi: 10.1002/humu.23386. Epub 2018 Jan 17. Hum Mutat. 2018. PMID: 29266534 Free PMC article. Review.
Single-Cell Transcriptomics Analysis of Human Small Antral Follicles.
Fan X, Moustakas I, Bialecka M, Del Valle JS, Overeem AW, Louwe LA, Pilgram GSK, van der Westerlaken LAJ, Mei H, Chuva de Sousa Lopes SM. Fan X, et al. Among authors: overeem aw. Int J Mol Sci. 2021 Nov 4;22(21):11955. doi: 10.3390/ijms222111955. Int J Mol Sci. 2021. PMID: 34769386 Free PMC article.
Myo5b knockout mice as a model of microvillus inclusion disease.
Cartón-García F, Overeem AW, Nieto R, Bazzocco S, Dopeso H, Macaya I, Bilic J, Landolfi S, Hernandez-Losa J, Schwartz S Jr, Ramon y Cajal S, van Ijzendoorn SC, Arango D. Cartón-García F, et al. Among authors: overeem aw. Sci Rep. 2015 Jul 23;5:12312. doi: 10.1038/srep12312. Sci Rep. 2015. PMID: 26201991 Free PMC article.
16 results