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Modeling congenital kidney diseases in Xenopus laevis.
Dis Model Mech. 2019 Apr 9;12(4):dmm038604. doi: 10.1242/dmm.038604.
Dis Model Mech. 2019.
PMID: 30967415
Free PMC article.
Review.
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.
Blackburn ATM, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, Al-Gazali L, Mohamed Saeed Mohamed Al Shamsi A, Gomez-Ospina N, Chao HT, Mirzaa GM, Scheuerle AE, Kukolich MK, Scaglia F, Eng C, Willsey HR, Braun MC, Lamb DJ, Miller RK, Bekheirnia MR.
Blackburn ATM, et al.
Genet Med. 2019 Dec;21(12):2755-2764. doi: 10.1038/s41436-019-0576-0. Epub 2019 Jul 2.
Genet Med. 2019.
PMID: 31263215
Free PMC article.
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A catenin of the plakophilin-subfamily, Pkp3, responds to canonical-Wnt pathway components and signals.
Hong JY, Zapata J, Blackburn A, Baumert R, Bae SM, Ji H, Nam HJ, Miller RK, McCrea PD.
Hong JY, et al.
Biochem Biophys Res Commun. 2021 Jul 23;563:31-39. doi: 10.1016/j.bbrc.2021.05.043. Epub 2021 May 28.
Biochem Biophys Res Commun. 2021.
PMID: 34058472
Free PMC article.
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Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.
Blackburn ATM, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, Al-Gazali L, Shamsi AMSMA, Gomez-Ospina N, Chao HT, Mirzaa GM, Scheuerle AE, Kukolich MK, Scaglia F, Eng C, Willsey HR, Braun MC, Lamb DJ, Miller RK, Bekheirnia MR.
Blackburn ATM, et al.
Genet Med. 2020 Apr;22(4):821. doi: 10.1038/s41436-019-0732-6.
Genet Med. 2020.
PMID: 31857706
Free article.
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