scholarly article | Q13442814 |
P2093 | author name string | Loredana Quadro | |
Wei Liu | |||
Ales Cvekl | |||
Qing Xie | |||
Lesley Wassef | |||
Karen Niederreither | |||
Mark Maconochie | |||
Alan Shanske | |||
Dorothy A. Frenz | |||
P2860 | cites work | Fibroblast growth factors | Q24542507 |
Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia | Q24675510 | ||
Inhibition of aldehyde dehydrogenase and retinoid signaling induces the expansion of human hematopoietic stem cells | Q24676524 | ||
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia | Q24680303 | ||
Embryonic retinoic acid synthesis is essential for early mouse post-implantation development | Q28140751 | ||
Mammalian MAP kinase signalling cascades | Q28204140 | ||
Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear | Q28255617 | ||
Fibroblast growth factor signaling during early vertebrate development | Q28305654 | ||
FGF/FGFR-2(IIIb) signaling is essential for inner ear morphogenesis | Q28506828 | ||
Identification of cis-element regulating expression of the mouse Fgf10 gene during inner ear development | Q28506880 | ||
Requirement of mesodermal retinoic acid generated by Raldh2 for posterior neural transformation | Q28584839 | ||
Requirements for FGF3 and FGF10 during inner ear formation | Q28585124 | ||
Differential requirements for FGF3, FGF8 and FGF10 during inner ear development | Q28585590 | ||
Fgf3 and Fgf10 are required for mouse otic placode induction | Q28585848 | ||
The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway | Q28589239 | ||
Dlx5 and Dlx6 homeobox genes are required for specification of the mammalian vestibular apparatus | Q28593442 | ||
Retinyl ester formation by lecithin: retinol acyltransferase is a key regulator of retinoid homeostasis in mouse embryogenesis | Q28593582 | ||
The regulation of AP-1 activity by mitogen-activated protein kinases | Q29620431 | ||
Expression of ERK signaling inhibitors Dusp6, Dusp7, and Dusp9 during mouse ear development | Q30491894 | ||
Temporal bone histopathology in experimental hypovitaminosis A | Q30873662 | ||
Multiple functions of Dlx genes | Q34075616 | ||
Specification of neuronal fates in the ventral neural tube | Q34141441 | ||
Function of vitamin A in vertebrate embryonic development | Q34174717 | ||
Three habits of highly effective signaling pathways: principles of transcriptional control by developmental cell signaling | Q34649230 | ||
Retinoic acid embryopathy | Q34686260 | ||
Retinoid signaling in inner ear development | Q36475161 | ||
Retinoic acid and hindbrain patterning | Q36475165 | ||
Ultrastructural changes in the organ of Corti and in the ganglion spiral cochleae after vitamin A deficiency | Q36495649 | ||
Transcriptional regulation of the mouse alpha A-crystallin gene: activation dependent on a cyclic AMP-responsive element (DE1/CRE) and a Pax-6-binding site | Q36566444 | ||
Dominant negative retinoid X receptor beta inhibits retinoic acid-responsive gene regulation in embryonal carcinoma cells | Q36643491 | ||
A complex array of positive and negative elements regulates the chicken alpha A-crystallin gene: involvement of Pax-6, USF, CREB and/or CREM, and AP-1 proteins | Q36669554 | ||
Metabolism of retinol during mammalian placental and embryonic development. | Q36763121 | ||
Expression and function of FGF10 in mammalian inner ear development | Q37524712 | ||
Fibroblast growth factor receptor signaling crosstalk in skeletogenesis | Q37806468 | ||
Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5. | Q38322087 | ||
Transforming growth factor-beta1 signaling participates in the physiological and pathological regulation of mouse inner ear development by all-trans retinoic acid | Q38328684 | ||
Fgf3 is required for dorsal patterning and morphogenesis of the inner ear epithelium | Q38440251 | ||
Relationship between the genomic organization and the overlapping embryonic expression patterns of the zebrafish dlx genes | Q38463218 | ||
Mutations in different components of FGF signaling in LADD syndrome | Q39746901 | ||
Involvement of retinoic acid/retinoid receptors in the regulation of murine alphaB-crystallin/small heat shock protein gene expression in the lens | Q41028490 | ||
Effects of retinoic acid excess on expression of Hox-2.9 and Krox-20 and on morphological segmentation in the hindbrain of mouse embryos | Q41082593 | ||
Dlx5 regulates regional development of the branchial arches and sensory capsules | Q41683496 | ||
Distinct functions for Aldh1 and Raldh2 in the control of ligand production for embryonic retinoid signaling pathways | Q42124664 | ||
Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3. | Q43075221 | ||
The retinoic acid receptors RARalpha and RARgamma are required for inner ear development | Q44237536 | ||
Transforming growth factor beta 1 is an epithelial-derived signal peptide that influences otic capsule formation | Q44802139 | ||
Congenital malformations of the external, middle, and inner ear produced by isotretinoin exposure in mouse embryos | Q44961489 | ||
Sensitive analysis of retinyl esters by isocratic adsorption chromatography. | Q46367394 | ||
Distinct roles for hindbrain and paraxial mesoderm in the induction and patterning of the inner ear revealed by a study of vitamin-A-deficient quail. | Q46615108 | ||
Inner ear malformations induced by isotretinoin in hamster fetuses | Q46673754 | ||
Changes in retinoic acid signaling alter otic patterning | Q47073410 | ||
Regulatory analysis of the mouse Fgf3 gene: control of embryonic expression patterns and dependence upon sonic hedgehog (Shh) signalling | Q47701725 | ||
Vitamin A-deficient quail embryos have half a hindbrain and other neural defects | Q49036731 | ||
Vitamin A deficiency results in the dose-dependent acquisition of anterior character and shortening of the caudal hindbrain of the rat embryo | Q49082681 | ||
Deletion mapping of split hand/split foot malformation with hearing impairment: a case report | Q50482215 | ||
Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH. | Q51907901 | ||
Retinoic acid-induced inner ear teratogenesis caused by defective Fgf3/Fgf10-dependent Dlx5 signaling. | Q51959559 | ||
Hindbrain respecification in the retinoid-deficient quail. | Q52173212 | ||
Differential distribution of retinoic acid synthesis in the chicken embryo as determined by immunolocalization of the retinoic acid synthetic enzyme, RALDH-2. | Q52176607 | ||
Role of a conserved retinoic acid response element in rhombomere restriction of Hoxb-1. | Q52214207 | ||
A conserved retinoic acid response element required for early expression of the homeobox gene Hoxb-1. | Q52215015 | ||
Epithelial control of periotic mesenchyme chondrogenesis. | Q52237633 | ||
Citral, an Inhibitor of Retinoic Acid Synthesis, Modifies Chick Limb Development | Q59538203 | ||
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia | Q62937771 | ||
Retinoid-induced ear malformations | Q68375139 | ||
Growth of the inner ear in organ culture | Q69357049 | ||
Retinoic acid-induced embryopathy of the mouse inner ear | Q71701777 | ||
Treatment with all-trans-retinoic acid decreases levels of endogenous TGF-beta(1) in the mesenchyme of the developing mouse inner ear | Q73547715 | ||
Effect of retinoic acid on otic capsule chondrogenesis in high-density culture suggests disruption of epithelial-mesenchymal interactions | Q73964929 | ||
Specificity within the ets family of transcription factors | Q77113231 | ||
The ETS-domain transcription factor family | Q77199453 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2947-2961 | |
P577 | publication date | 2010-12-01 | |
P1433 | published in | American Journal of Medical Genetics | Q4744254 |
P1476 | title | Retinoid signaling in inner ear development: A "Goldilocks" phenomenon | |
Retinoid signaling in inner ear development: A “Goldilocks” phenomenon | |||
P478 | volume | 152A |
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Q34452016 | RA and FGF signalling are required in the zebrafish otic vesicle to pattern and maintain ventral otic identities |
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Q37642802 | The best-laid plans go oft awry: synaptogenic growth factor signaling in neuropsychiatric disease. |
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Q35990963 | Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia). |
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