Found: 27
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Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15885-1
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- Article
Proteomic profiling of retina and retinal pigment epithelium combined embryonic tissue to facilitate ocular disease gene discovery.
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- Human Genetics, 2023, v. 142, n. 7, p. 927, doi. 10.1007/s00439-023-02570-0
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- Article
Oral mesotherapy technique for the treatment of physiologic gingival melanin hyperpigmentation using locally injectable vitamin C: a clinical and histologic cases series.
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- Quintessence International, 2022, v. 53, n. 7, p. 580, doi. 10.3290/j.qi.b3044857
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- Article
iSyTE 2.0: a database for expression-based gene discovery in the eye.
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- Nucleic Acids Research, 2018, v. 46, n. D1, p. D875, doi. 10.1093/nar/gkx837
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- Article
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23873-8
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- Article
The RNA-binding protein Celf1 post-transcriptionally regulates p27<sup>Kip1</sup> and Dnase2b to control fiber cell nuclear degradation in lens development.
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- PLoS Genetics, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pgen.1007278
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- Article
Misconduct in Biomedical Research: A Meta-Analysis and Systematic Review.
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- Journal of International Society of Preventive & Community Dentistry, 2023, v. 13, n. 3, p. 185, doi. 10.4103/jispcd.JISPCD_220_22
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- Article
Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.
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- Birth Defects Research, 2017, v. 109, n. 1, p. 27, doi. 10.1002/bdra.23596
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- Article
MS/MS in silico subtraction-based proteomic profiling as an approach to facilitate disease gene discovery: application to lens development and cataract.
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- Human Genetics, 2020, v. 139, n. 2, p. 151, doi. 10.1007/s00439-019-02095-5
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- Article
High-throughput transcriptome analysis reveals that the loss of Pten activates a novel NKX6-1/RASGRP1 regulatory module to rescue microphthalmia caused by Fgfr2-deficient lenses.
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- Human Genetics, 2019, v. 138, n. 11/12, p. 1391, doi. 10.1007/s00439-019-02084-8
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- Article
RNA sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery.
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- Human Genetics, 2018, v. 137, n. 11/12, p. 941, doi. 10.1007/s00439-018-1958-0
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- Article
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract.
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- Human Genetics, 2017, v. 136, n. 2, p. 205, doi. 10.1007/s00439-016-1747-6
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- Article
Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract.
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- Human Genetics, 2015, v. 134, n. 7, p. 717, doi. 10.1007/s00439-015-1554-5
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- Article
Carbon nanotube-textured sand for controlling bioavailability of contaminated sediments.
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- Nano Research, 2010, v. 3, n. 6, p. 412, doi. 10.1007/s12274-010-1046-9
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- Article
Variant Analyses of Candidate Genes in Orofacial Clefts in Multi‐Ethnic Populations.
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- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.03614
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- Article
The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology.
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- Human Molecular Genetics, 2020, v. 29, n. 12, p. 2076, doi. 10.1093/hmg/ddaa096
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- Article
Marker-assisted improvement of bacterial blight resistance in parental lines of Pusa RH10, a superfine grain aromatic rice hybrid.
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- Molecular Breeding, 2010, v. 26, n. 2, p. 293, doi. 10.1007/s11032-010-9407-3
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- Article
High-Throughput Transcriptomics of Celf1 Conditional Knockout Lens Identifies Downstream Networks Linked to Cataract Pathology.
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- Cells (2073-4409), 2023, v. 12, n. 7, p. 1070, doi. 10.3390/cells12071070
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- Article
Lens Epithelial Explants Treated with Vitreous Humor Undergo Alterations in Chromatin Landscape with Concurrent Activation of Genes Associated with Fiber Cell Differentiation and Innate Immune Response.
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- Cells (2073-4409), 2023, v. 12, n. 3, p. 501, doi. 10.3390/cells12030501
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- Article
Front Cover, Volume 40, Issue 10.
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- Human Mutation, 2019, v. 40, n. 10, p. i, doi. 10.1002/humu.23923
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- Article
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
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- Human Mutation, 2019, v. 40, n. 10, p. 1813, doi. 10.1002/humu.23793
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- Article
Cover Image, Volume 39, Issue 4.
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- Human Mutation, 2018, v. 39, n. 4, p. i, doi. 10.1002/humu.23414
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Mutation update of transcription factor genes <italic>FOXE3</italic>, <italic>HSF4</italic>, <italic>MAF</italic>, and <italic>PITX3</italic> causing cataracts and other developmental ocular defects.
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- Human Mutation, 2018, v. 39, n. 4, p. 471, doi. 10.1002/humu.23395
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- Article
Variant analyses of candidate genes in orofacial clefts in multi‐ethnic populations.
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- Oral Diseases, 2022, v. 28, n. 7, p. 1921, doi. 10.1111/odi.13932
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- Article
Shared genetic risk between major orofacial cleft phenotypes in an African population.
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- Genetic Epidemiology, 2024, v. 48, n. 6, p. 258, doi. 10.1002/gepi.22564
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- Article
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals.
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- Genetic Epidemiology, 2019, v. 43, n. 6, p. 704, doi. 10.1002/gepi.22214
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- Article
ROLE OF PROBIOTICS AS AN ADJUNCT TO SCALING AND ROOT PLANING IN CHRONIC PERIODONTITIS PATIENTS.
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- International Poster Journal of Dentistry & Oral Medicine, 2023, n. 4, p. 1
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- Article