Oh S, Jeon J, Je S, Kim S, Jung J, Ko H
Cell Commun Signal. 2024; 22(1):482.
PMID: 39385148
PMC: 11465819.
DOI: 10.1186/s12964-024-01855-9.
Zeni C, Komiya Y, Habas R
Dev Biol. 2024; 515:18-29.
PMID: 38945423
PMC: 11317212.
DOI: 10.1016/j.ydbio.2024.06.019.
Kacker S, Parsad V, Singh N, Hordiichuk D, Alvarez S, Gohar M
J Dev Biol. 2024; 12(2).
PMID: 38804432
PMC: 11130840.
DOI: 10.3390/jdb12020012.
Vuong L, Mlodzik M
Curr Top Dev Biol. 2023; 155:95-125.
PMID: 38043953
PMC: 11287783.
DOI: 10.1016/bs.ctdb.2023.09.002.
Humphries A, Molina-Pelayo C, Sil P, Hazelett C, Devenport D, Mlodzik M
PLoS Genet. 2023; 19(7):e1010849.
PMID: 37463168
PMC: 10381084.
DOI: 10.1371/journal.pgen.1010849.
Balancing WNT signalling in early forebrain development: The role of LRP4 as a modulator of LRP6 function.
Geng S, Paul F, Kowalczyk I, Raimundo S, Sporbert A, Mamo T
Front Cell Dev Biol. 2023; 11:1173688.
PMID: 37091972
PMC: 10119419.
DOI: 10.3389/fcell.2023.1173688.
CIC missense variants contribute to susceptibility for spina bifida.
Han X, Cao X, Aguiar-Pulido V, Yang W, Karki M, Ramirez P
Hum Mutat. 2022; 43(12):2021-2032.
PMID: 36054333
PMC: 9772115.
DOI: 10.1002/humu.24460.
The role of Lrp6-mediated Wnt/β-catenin signaling in the development and intervention of spinal neural tube defects in mice.
Zhao T, McMahon M, Reynolds K, Saha S, Stokes A, Zhou C
Dis Model Mech. 2022; 15(6).
PMID: 35514236
PMC: 9194482.
DOI: 10.1242/dmm.049517.
The regulatory roles of motile cilia in CSF circulation and hydrocephalus.
Kumar V, Umair Z, Kumar S, Goutam R, Park S, Kim J
Fluids Barriers CNS. 2021; 18(1):31.
PMID: 34233705
PMC: 8261947.
DOI: 10.1186/s12987-021-00265-0.
nNOS regulates ciliated cell polarity, ciliary beat frequency, and directional flow in mouse trachea.
Mikhailik A, Michurina T, Dikranian K, Hearn S, Maxakov V, Siller S
Life Sci Alliance. 2021; 4(5).
PMID: 33653689
PMC: 8008965.
DOI: 10.26508/lsa.202000981.
Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.
Au K, Hebert L, Hillman P, Baker C, Brown M, Kim D
Sci Rep. 2021; 11(1):3639.
PMID: 33574475
PMC: 7878900.
DOI: 10.1038/s41598-021-83058-7.
A null allele of Dnaaf2 displays embryonic lethality and mimics human ciliary dyskinesia.
Cheong A, Degani R, Tremblay K, Mager J
Hum Mol Genet. 2019; 28(16):2775-2784.
PMID: 31107948
PMC: 6688062.
DOI: 10.1093/hmg/ddz106.
A deficiency in SUMOylation activity disrupts multiple pathways leading to neural tube and heart defects in Xenopus embryos.
Bertke M, Dubiak K, Cronin L, Zeng E, Huber P
BMC Genomics. 2019; 20(1):386.
PMID: 31101013
PMC: 6525467.
DOI: 10.1186/s12864-019-5773-3.
Neural control of body-plan axis in regenerating planaria.
Pietak A, Bischof J, LaPalme J, Morokuma J, Levin M
PLoS Comput Biol. 2019; 15(4):e1006904.
PMID: 30990801
PMC: 6485777.
DOI: 10.1371/journal.pcbi.1006904.
Ciliary and cytoskeletal functions of an ancient monooxygenase essential for bioactive amidated peptide synthesis.
Kumar D, Mains R, Eipper B, King S
Cell Mol Life Sci. 2019; 76(12):2329-2348.
PMID: 30879092
PMC: 6529398.
DOI: 10.1007/s00018-019-03065-w.
La-related protein 6 controls ciliated cell differentiation.
Manojlovic Z, Earwood R, Kato A, Perez D, Cabrera O, Didier R
Cilia. 2017; 6:4.
PMID: 28344782
PMC: 5364628.
DOI: 10.1186/s13630-017-0047-7.
Fetal DNA hypermethylation in tight junction pathway is associated with neural tube defects: A genome-wide DNA methylation analysis.
Wang L, Lin S, Zhang J, Tian T, Jin L, Ren A
Epigenetics. 2017; 12(2):157-165.
PMID: 28059605
PMC: 5330433.
DOI: 10.1080/15592294.2016.1277298.
Digenic mutations of human paralogs in Dent's disease type 2 associated with Chiari I malformation.
Duran D, Jin S, DeSpenza Jr T, Nelson-Williams C, Cogal A, Abrash E
Hum Genome Var. 2016; 3:16042.
PMID: 28018608
PMC: 5143364.
DOI: 10.1038/hgv.2016.42.
G-protein-coupled receptor signaling and neural tube closure defects.
Shimada I, Mukhopadhyay S
Birth Defects Res. 2016; 109(2):129-139.
PMID: 27731925
PMC: 5388587.
DOI: 10.1002/bdra.23567.
The E3 ubiquitin ligase Hace1 is required for early embryonic development in Xenopus laevis.
Iimura A, Yamazaki F, Suzuki T, Endo T, Nishida E, Kusakabe M
BMC Dev Biol. 2016; 16(1):31.
PMID: 27653971
PMC: 5031333.
DOI: 10.1186/s12861-016-0132-y.