Year |
Citation |
Score |
2020 |
Goodman T, Nayar SG, Clare S, Mikolajczak M, Rice R, Mansour S, Bellusci S, Hajihosseini MK. Fibroblast growth factor 10 is a negative regulator of postnatal neurogenesis in the mouse hypothalamus. Development (Cambridge, England). 147. PMID 32661019 DOI: 10.1242/Dev.180950 |
0.425 |
|
2020 |
Urness LD, Wang X, Li C, Quadros RM, Harms DW, Gurumurthy CB, Mansour SL. , a new CRE driver to regulate gene expression in the otic placode lineage and other FGFR2b-dependent epithelia. Development (Cambridge, England). PMID 32541002 DOI: 10.1242/Dev.191015 |
0.465 |
|
2018 |
Urness LD, Wang X, Doan H, Shumway N, Noyes CA, Gutierrez-Magana E, Lu R, Mansour SL. Spatial and temporal inhibition of FGFR2b ligands reveals continuous requirements and novel targets in mouse inner ear morphogenesis. Development (Cambridge, England). 145. PMID 30504125 DOI: 10.1242/Dev.170142 |
0.594 |
|
2017 |
Quadros RM, Miura H, Harms DW, Akatsuka H, Sato T, Aida T, Redder R, Richardson GP, Inagaki Y, Sakai D, Buckley SM, Seshacharyulu P, Batra SK, Behlke MA, Zeiner SA, ... ... Mansour SL, et al. Easi-CRISPR: a robust method for one-step generation of mice carrying conditional and insertion alleles using long ssDNA donors and CRISPR ribonucleoproteins. Genome Biology. 18: 92. PMID 28511701 DOI: 10.1186/S13059-017-1220-4 |
0.32 |
|
2016 |
Ohta S, Wang B, Mansour SL, Schoenwolf GC. SHH Ventralizes the Otocyst by Maintaining Basal PKA Activity and Regulating GLI3 Signaling. Developmental Biology. PMID 27720745 DOI: 10.1016/J.Ydbio.2016.10.004 |
0.46 |
|
2016 |
Ohta S, Wang B, Mansour SL, Schoenwolf GC. BMP regulates regional gene expression in the dorsal otocyst through canonical and non-canonical intracellular pathways. Development (Cambridge, England). PMID 27151948 DOI: 10.1242/Dev.137133 |
0.519 |
|
2015 |
Urness LD, Wang X, Shibata S, Ohyama T, Mansour SL. Fgf10 is required for specification of non-sensory regions of the cochlear epithelium. Developmental Biology. 400: 59-71. PMID 25624266 DOI: 10.1016/J.Ydbio.2015.01.015 |
0.585 |
|
2014 |
Jackson A, Kasah S, Mansour SL, Morrow B, Basson MA. Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 243: 1143-51. PMID 24812002 DOI: 10.1002/Dvdy.24147 |
0.614 |
|
2013 |
Mansour SL, Li C, Urness LD. Genetic rescue of Muenke syndrome model hearing loss reveals prolonged FGF-dependent plasticity in cochlear supporting cell fates. Genes & Development. 27: 2320-31. PMID 24145799 DOI: 10.1101/Gad.228957.113 |
0.463 |
|
2011 |
Urness LD, Bleyl SB, Wright TJ, Moon AM, Mansour SL. Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development. Developmental Biology. 356: 383-97. PMID 21664901 DOI: 10.1016/J.Ydbio.2011.05.671 |
0.534 |
|
2010 |
Ohta S, Mansour SL, Schoenwolf GC. BMP/SMAD signaling regulates the cell behaviors that drive the initial dorsal-specific regional morphogenesis of the otocyst. Developmental Biology. 347: 369-81. PMID 20837004 DOI: 10.1016/J.Ydbio.2010.09.002 |
0.458 |
|
2010 |
Urness LD, Paxton CN, Wang X, Schoenwolf GC, Mansour SL. FGF signaling regulates otic placode induction and refinement by controlling both ectodermal target genes and hindbrain Wnt8a. Developmental Biology. 340: 595-604. PMID 20171206 DOI: 10.1016/J.Ydbio.2010.02.016 |
0.647 |
|
2010 |
Urness LD, Wright TJ, Mansour SL. Program/Abstract # 229Fgf3 and Fgf10 are required redundantly for neural crest migration and cardiovascular development Developmental Biology. 344. DOI: 10.1016/J.Ydbio.2010.05.273 |
0.47 |
|
2010 |
Urness LD, Wright TJ, Mansour SL. Fgf3 and Fgf10 are required redundantly for neural crest migration and cardiovascular development Developmental Biology. 344: 481. DOI: 10.1016/J.Ydbio.2009.05.405 |
0.539 |
|
2009 |
Abler LL, Mansour SL, Sun X. Conditional gene inactivation reveals roles for Fgf10 and Fgfr2 in establishing a normal pattern of epithelial branching in the mouse lung. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 1999-2013. PMID 19618463 DOI: 10.1002/Dvdy.22032 |
0.439 |
|
2009 |
Mansour SL, Twigg SR, Freeland RM, Wall SA, Li C, Wilkie AO. Hearing loss in a mouse model of Muenke syndrome. Human Molecular Genetics. 18: 43-50. PMID 18818193 DOI: 10.1093/Hmg/Ddn311 |
0.411 |
|
2009 |
Hatch EP, Urness LD, Mansour SL. Fgf16(IRESCre) mice: a tool to inactivate genes expressed in inner ear cristae and spiral prominence epithelium. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 358-66. PMID 18773497 DOI: 10.1002/Dvdy.21681 |
0.773 |
|
2009 |
Urness LD, Wright TJ, Mansour SL. Fgf3 and Fgf10 are required redundantly for neural crest migration and cardiovascular development Developmental Biology. 331: 494. DOI: 10.1016/J.YDBIO.2009.05.405 |
0.456 |
|
2009 |
Noyes CA, Want X, Hatch EP, Mansour SL. 13-P077 FGF signaling in OTIC morphogenesis Mechanisms of Development. 126: S217-S218. DOI: 10.1016/J.Mod.2009.06.550 |
0.735 |
|
2008 |
Urness LD, Li C, Wang X, Mansour SL. Expression of ERK signaling inhibitors Dusp6, Dusp7, and Dusp9 during mouse ear development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 163-9. PMID 18058922 DOI: 10.1002/Dvdy.21380 |
0.629 |
|
2007 |
Hatch EP, Noyes CA, Wang X, Wright TJ, Mansour SL. Fgf3 is required for dorsal patterning and morphogenesis of the inner ear epithelium. Development (Cambridge, England). 134: 3615-25. PMID 17855431 DOI: 10.1242/Dev.006627 |
0.76 |
|
2007 |
Li C, Scott DA, Hatch E, Tian X, Mansour SL. Dusp6 (Mkp3) is a negative feedback regulator of FGF-stimulated ERK signaling during mouse development. Development (Cambridge, England). 134: 167-76. PMID 17164422 DOI: 10.1242/Dev.02701 |
0.733 |
|
2006 |
Hatch E, Wang X, Mansour S. The roles of mouse Fgf16 and Fgf3 during inner ear development Developmental Biology. 295: 396. DOI: 10.1016/J.Ydbio.2006.04.214 |
0.762 |
|
2005 |
Ladher RK, Wright TJ, Moon AM, Mansour SL, Schoenwolf GC. FGF8 initiates inner ear induction in chick and mouse. Genes & Development. 19: 603-13. PMID 15741321 DOI: 10.1101/Gad.1273605 |
0.651 |
|
2004 |
Satoh Y, Haraguchi R, Wright TJ, Mansour SL, Partanen J, Hajihosseini MK, Eswarakumar VP, Lonai P, Yamada G. Regulation of external genitalia development by concerted actions of FGF ligands and FGF receptors. Anatomy and Embryology. 208: 479-86. PMID 15340846 DOI: 10.1007/S00429-004-0419-9 |
0.623 |
|
2004 |
Wright TJ, Ladher R, McWhirter J, Murre C, Schoenwolf GC, Mansour SL. Mouse FGF15 is the ortholog of human and chick FGF19, but is not uniquely required for otic induction. Developmental Biology. 269: 264-75. PMID 15081372 DOI: 10.1016/J.Ydbio.2004.02.003 |
0.65 |
|
2003 |
Wright TJ, Mansour SL. FGF signaling in ear development and innervation. Current Topics in Developmental Biology. 57: 225-59. PMID 14674483 DOI: 10.1016/S0070-2153(03)57008-9 |
0.632 |
|
2003 |
Wright TJ, Hatch EP, Karabagli H, Karabagli P, Schoenwolf GC, Mansour SL. Expression of mouse fibroblast growth factor and fibroblast growth factor receptor genes during early inner ear development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 228: 267-72. PMID 14517998 DOI: 10.1002/Dvdy.10362 |
0.764 |
|
2003 |
Wright TJ, Mansour SL. Fgf3 and Fgf10 are required for mouse otic placode induction. Development (Cambridge, England). 130: 3379-90. PMID 12810586 DOI: 10.1242/Dev.00555 |
0.665 |
|
2001 |
Yang W, Li C, Mansour SL. Impaired motor coordination in mice that lack punc. Molecular and Cellular Biology. 21: 6031-43. PMID 11486040 DOI: 10.1128/Mcb.21.17.6031-6043.2001 |
0.407 |
|
1999 |
Yang W, Mansour SL. Expression and genetic analysis of prtb, a gene that encodes a highly conserved proline-rich protein expressed in the brain. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 215: 108-16. PMID 10373015 DOI: 10.1002/(Sici)1097-0177(199906)215:2<108::Aid-Dvdy3>3.0.Co;2-I |
0.393 |
|
1998 |
Yang W, Musci TS, Mansour SL. Trapping genes expressed in the developing mouse inner ear. Hearing Research. 114: 53-61. PMID 9447918 DOI: 10.1016/S0378-5955(97)00146-9 |
0.4 |
|
1995 |
Mansour SL. Targeted disruption of int-2 (fgf-3) causes developmental defects in the tail and inner ear. Molecular Reproduction and Development. 39: 62-7; discussion 67-. PMID 7999362 DOI: 10.1002/Mrd.1080390111 |
0.487 |
|
1991 |
Mansour SL. Gene targeting in murine embryonic stem cells: introduction of specific alterations into the mammalian genome. Genetic Analysis, Techniques and Applications. 7: 219-27. PMID 2091698 DOI: 10.1016/0735-0651(90)90004-Y |
0.327 |
|
1990 |
Mansour SL, Thomas KR, Deng CX, Capecchi MR. Introduction of a lacZ reporter gene into the mouse int-2 locus by homologous recombination. Proceedings of the National Academy of Sciences of the United States of America. 87: 7688-92. PMID 2120706 DOI: 10.1073/Pnas.87.19.7688 |
0.339 |
|
1988 |
Mansour SL, Thomas KR, Capecchi MR. Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes. Nature. 336: 348-52. PMID 3194019 DOI: 10.1038/336348A0 |
0.335 |
|
1988 |
Mansour SL, Martin GR. Four classes of mRNA are expressed from the mouse int-2 gene, a member of the FGF gene family. The Embo Journal. 7: 2035-2041. DOI: 10.1002/J.1460-2075.1988.Tb03043.X |
0.351 |
|
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