Related references
Note: Only part of the references are listed.PIWI-interacting RNA sequencing profiles in maternal plasma-derived exosomes reveal novel non-invasive prenatal biomarkers for the early diagnosis of nonsyndromic cleft lip and palate
Shanshan Jia et al.
EBIOMEDICINE (2021)
Diagnostic accuracy of fetal MRI to detect cleft palate: a meta-analysis
Hanneke E. M. van der Hoek-Snieders et al.
EUROPEAN JOURNAL OF PEDIATRICS (2020)
Genome-wide Identification of Foxf2 Target Genes in Palate Development
J. Xu et al.
JOURNAL OF DENTAL RESEARCH (2020)
Clinical application of exosomes and circulating microRNAs in the diagnosis of pregnancy complications and foetal abnormalities
Haiou Yang et al.
JOURNAL OF TRANSLATIONAL MEDICINE (2020)
Complement factors and alpha-fetoprotein as biomarkers for noninvasive prenatal diagnosis of neural tube defects
Naixuan Dong et al.
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES (2020)
Effects of small interfering RNA-mediated silencing of susceptibility genes of non-syndromic cleft lip with or without cleft palate on cell proliferation and migration
Meng-Xue Li et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2020)
Wnt signaling in orofacial clefts: crosstalk, pathogenesis and models
Kurt Reynolds et al.
DISEASE MODELS & MECHANISMS (2019)
The prenatal diagnosis and classification of cleft palate: the role and value of magnetic resonance imaging
Weizeng Zheng et al.
EUROPEAN RADIOLOGY (2019)
Perturbed development of cranial neural crest cells in association with reduced sonic hedgehog signaling underlies the pathogenesis of retinoic-acid-induced cleft palate
Qi Wang et al.
DISEASE MODELS & MECHANISMS (2019)
Three GLI2 mutations combined potentially underlie non-syndromic cleft lip with or without cleft palate in a Chinese pedigree
Peiqi Meng et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2019)
Expression profile of maternal circulating microRNAs as non-invasive biomarkers for prenatal diagnosis of congenital heart defects
Hui Gu et al.
BIOMEDICINE & PHARMACOTHERAPY (2019)
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands
Karuna R. M. van der Meij et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
Quantitative Proteomics by SWATH-MS of Maternal Plasma Exosomes Determine Pathways Associated With Term and Preterm Birth
Ramkumar Menon et al.
ENDOCRINOLOGY (2019)
MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts: a meta-analysis
Min Gu et al.
EUROPEAN JOURNAL OF ORAL SCIENCES (2018)
Noninvasive blood tests for fetal development predict gestational age and preterm delivery
Thuy T. M. Ngo et al.
SCIENCE (2018)
Negotiating acceptable termination of pregnancy for non-lethal fetal anomaly: a qualitative study of professional perspectives
Lisa Crowe et al.
BMJ OPEN (2018)
Small-Molecule Inhibitors Disrupt let-7 Oligouridylation and Release the Selective Blockade of let-7 Processing by LIN28
Longfei Wang et al.
CELL REPORTS (2018)
Ectopic expression of Hoxb1 induces cardiac and craniofacial malformations
Stephane Zaffran et al.
GENESIS (2018)
Lin28 Signaling Supports Mammalian PNS and CNS Axon Regeneration
Xue-Wei Wang et al.
CELL REPORTS (2018)
Targeting YOD1 by RNA Interference Inhibits Proliferation and Migration of Human Oral Keratinocytes through Transforming Growth Factor-β3 Signaling Pathway
Xiao-Long Zhou et al.
BIOMED RESEARCH INTERNATIONAL (2018)
Folate deficiency disturbs hsa-let-7 g level through methylation regulation in neural tube defects
Li Wang et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2017)
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Yanqin Yu et al.
NATURE COMMUNICATIONS (2017)
Cell-Free DNA Screening
Matthew R. Grace et al.
OBSTETRICAL & GYNECOLOGICAL SURVEY (2016)
Elevated hsa-miR-99a levels in maternal plasma may indicate congenital heart defects
Lars Kehler et al.
BIOMEDICAL REPORTS (2015)
MicroRNA expression profiling of the developing murine upper lip
Dennis R. Warner et al.
DEVELOPMENT GROWTH & DIFFERENTIATION (2014)
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly
Kelly A. Bear et al.
JOURNAL OF MEDICAL GENETICS (2014)
Shh-mediated degradation of Hhip allows cell autonomous and non-cell autonomous Shh signalling
Lina Kwong et al.
NATURE COMMUNICATIONS (2014)
Genomic Approaches for Studying Craniofacial Disorders
Kriti D. Khandelwal et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2013)
microRNA expression profiling of the developing mouse heart
Li Cao et al.
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE (2012)
Diagnostic role of microRNA expression profile in the serum of pregnant women with fetuses with neural tube defects
Hui Gu et al.
JOURNAL OF NEUROCHEMISTRY (2012)
Prevalence at Birth of Cleft Lip With or Without Cleft Palate: Data From the International Perinatal Database of Typical Oral Clefts (IPDTOC)
Pierpaolo Mastroiacovo et al.
CLEFT PALATE-CRANIOFACIAL JOURNAL (2011)
Cleft lip and palate: understanding genetic and environmental influences
Michael J. Dixon et al.
NATURE REVIEWS GENETICS (2011)
The role of let-7 in cell differentiation and cancer
Benjamin Boyerinas et al.
ENDOCRINE-RELATED CANCER (2010)
Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder
N Gharani et al.
MOLECULAR PSYCHIATRY (2004)
Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts
P Stanier et al.
HUMAN MOLECULAR GENETICS (2004)
Msx homeobox gene family and craniofacial development
S Alappat et al.
CELL RESEARCH (2003)
Loss-of-function mutations in the human GL12 gene are associated with pituitary anomalies and holoprosencephaly-like features
E Roessler et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Bmp4 gene is expressed at the putative site of fusion in the midfacial region
SG Gong et al.
DIFFERENTIATION (2003)
Share Paper
