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2008 1
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Page 1
Aquatic models of human ciliary diseases.
Corkins ME, Krneta-Stankic V, Kloc M, Miller RK. Corkins ME, et al. Genesis. 2021 Feb;59(1-2):e23410. doi: 10.1002/dvg.23410. Epub 2021 Jan 26. Genesis. 2021. PMID: 33496382 Free PMC article. Review.
Divergent roles of the Wnt/PCP Formin Daam1 in renal ciliogenesis.
Corkins ME, Krneta-Stankic V, Kloc M, McCrea PD, Gladden AB, Miller RK. Corkins ME, et al. PLoS One. 2019 Aug 30;14(8):e0221698. doi: 10.1371/journal.pone.0221698. eCollection 2019. PLoS One. 2019. PMID: 31469868 Free PMC article.
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. Among authors: corkins me. 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.
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. Among authors: corkins me. Genet Med. 2020 Apr;22(4):821. doi: 10.1038/s41436-019-0732-6. Genet Med. 2020. PMID: 31857706 Free article.
18 results