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Ian C Welsh
Ian C Welsh
The Jackson Laboratory
在 cornell.edu 的电子邮件经过验证
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引用次数
引用次数
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Notch signaling regulates left–right asymmetry determination by inducing Nodal expression
LT Krebs, N Iwai, S Nonaka, IC Welsh, Y Lan, R Jiang, Y Saijoh, ...
Genes & development 17 (10), 1207-1212, 2003
2772003
Evidence for a conserved function in synapse formation reveals Phr1 as a candidate gene for respiratory failure in newborn mice
RW Burgess, KA Peterson, MJ Johnson, JJ Roix, IC Welsh, TP O'Brien
Molecular and cellular biology 24 (3), 1096-1105, 2004
1222004
Loss of extreme long-range enhancers in human neural crest drives a craniofacial disorder
HK Long, M Osterwalder, IC Welsh, K Hansen, JOJ Davies, YE Liu, ...
Cell stem cell 27 (5), 765-783. e14, 2020
1172020
The left-right Pitx2 pathway drives organ-specific arterial and lymphatic development in the intestine
A Mahadevan, IC Welsh, A Sivakumar, DW Gludish, AR Shilvock, ...
Developmental cell 31 (6), 690-706, 2014
1032014
A dosage-dependent role for Spry2 in growth and patterning during palate development
IC Welsh, A Hagge-Greenberg, TP O’Brien
Mechanisms of development 124 (9-10), 746-761, 2007
952007
Signaling integration in the rugae growth zone directs sequential SHH signaling center formation during the rostral outgrowth of the palate
IC Welsh, TP O'Brien
Developmental biology 336 (1), 53-67, 2009
912009
Systematic reconstruction of cellular trajectories across mouse embryogenesis
C Qiu, J Cao, BK Martin, T Li, IC Welsh, S Srivatsan, X Huang, D Calderon, ...
Nature genetics 54 (3), 328-341, 2022
892022
Integration of left-right Pitx2 transcription and Wnt signaling drives asymmetric gut morphogenesis via Daam2
IC Welsh, M Thomsen, DW Gludish, C Alfonso-Parra, Y Bai, JF Martin, ...
Developmental cell 26 (6), 629-644, 2013
882013
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass
RJ Munroe, V Prabhu, GM Acland, KR Johnson, BS Harris, TP O'Brien, ...
BMC developmental biology 9 (1), 1-9, 2009
612009
Chromatin architecture of the Pitx2 locus requires CTCF-and Pitx2-dependent asymmetry that mirrors embryonic gut laterality
IC Welsh, H Kwak, FL Chen, M Werner, LS Shopland, CG Danko, JT Lis, ...
Cell reports 13 (2), 337-349, 2015
362015
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research
BD Samuels, R Aho, JF Brinkley, A Bugacov, E Feingold, S Fisher, ...
Development 147 (18), 2020
292020
Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface
IC Welsh, J Hart, JM Brown, K Hansen, M Rocha Marques, RJ Aho, ...
Journal of anatomy 233 (2), 222-242, 2018
292018
Loss of Late Primitive Streak Mesoderm and Interruption of Left–Right Morphogenesis in the Ednrbs-1Acrg Mutant Mouse
IC Welsh, TP O'Brien
Developmental biology 225 (1), 151-168, 2000
272000
Analysis of the gene regulatory program induced by the homeobox transcription factor distal-less 3 in mouse placenta
L Han, M Dias Figueiredo, KA Berghorn, TN Iwata, PA Clark-Campbell, ...
Endocrinology 148 (3), 1246-1254, 2007
182007
A single-cell transcriptional timelapse of mouse embryonic development, from gastrula to pup
C Qiu, BK Martin, IC Welsh, RM Daza, TM Le, X Huang, EK Nichols, ...
bioRxiv, 2023.04. 05.535726, 2023
92023
Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice
AC Frank, KA Meyers, IC Welsh, TP O'Brien
Proceedings of the National Academy of Sciences 100 (24), 14103-14108, 2003
92003
A single-cell time-lapse of mouse prenatal development from gastrula to birth
C Qiu, BK Martin, IC Welsh, RM Daza, TM Le, X Huang, EK Nichols, ...
Nature, 1-10, 2024
82024
The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4
A Luzzio, S Edie, K Palmer, LB Caddle, R Urban, LO Goodwin, IC Welsh, ...
Mammalian Genome, 1-11, 2023
2023
Palatal segment contributions to midfacial growth in three inbred mouse strains
IC Welsh, M Feiler, D Lipman, I Mormile, K Hansen, CJC Percival
bioRxiv, 2023.10. 03.560703, 2023
2023
CRISPR/Cas9-based analysis of a missense variant in Paxip1 suggests subtle effects on palatal process distance
N Ishorst, EZ Kvon, Y Zhu, S Tran, I Plajzer-Frick, CS Pickle, S Hoelzel, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 245-245, 2020
2020
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