| P50 | author | Jean-Paul Borg | Q49224201 |
| | Tania M Puvirajesinghe | Q56852022 |
| P2093 | author name string | Jean-Paul Borg | |
| | Tania M Puvirajesinghe | |
| P2860 | cites work | Intermittent pattern of neural tube closure in two strains of mice | Q70664956 |
| | Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice | Q72116911 |
| | Quantitative analysis of the toxicity of human amniotic fluid to cultured rat spinal cord | Q74522820 |
| | A proteomic approach for the characterization of C677T mutation of the human gene methylenetetrahydrofolate reductase | Q80218974 |
| | Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model | Q80847027 |
| | Proteomic analysis of amniotic fluid of pregnant rats with spina bifida aperta | Q82634486 |
| | Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies | Q21089859 |
| | Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways | Q24302034 |
| | A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis | Q24311615 |
| | Identification of novel rare mutations of DACT1 in human neural tube defects | Q24324120 |
| | A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase | Q24324172 |
| | The balance between isoforms of the prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs | Q24599652 |
| | High-throughput generation of tagged stable cell lines for proteomic analysis | Q27331566 |
| | Flamingo, a seven-pass transmembrane cadherin, regulates planar cell polarity under the control of Frizzled | Q28144517 |
| | Molecular analysis of the gene for the human vitamin-D-binding protein (group-specific component): allelic differences of the common genetic GC types | Q28182423 |
| | Molecular basis for the three major forms of human serum vitamin D binding protein (group-specific component) | Q28246249 |
| | The Drosophila segment polarity gene dishevelled encodes a novel protein required for response to the wingless signal | Q28258603 |
| | Homocysteine and cardiovascular disease | Q28265188 |
| | Mutations in VANGL1 associated with neural-tube defects | Q28296545 |
| | Curly tail: a 50-year history of the mouse spina bifida model | Q28366531 |
| | Molecular characterisation of endogenous Vangl2/Vangl1 heteromeric protein complexes | Q28484108 |
| | The Grainyhead-like epithelial transactivator Get-1/Grhl3 regulates epidermal terminal differentiation and interacts functionally with LMO4 | Q28505730 |
| | Regional neural tube closure defined by the Grainy head-like transcription factors | Q28506595 |
| | apo B gene knockout in mice results in embryonic lethality in homozygotes and neural tube defects, male infertility, and reduced HDL cholesterol ester and apo A-I transport rates in heterozygotes | Q28507091 |
| | Folic acid prevents exencephaly in Cited2 deficient mice | Q28507567 |
| | Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3 | Q28507977 |
| | Crooked tail (Cd) models human folate-responsive neural tube defects | Q28508865 |
| | Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in mice | Q28513087 |
| | Posterior malformations in Dact1 mutant mice arise through misregulated Vangl2 at the primitive streak | Q28587276 |
| | Identification and characterization of Grainyhead-like epithelial transactivator (GET-1), a novel mammalian Grainyhead-like factor | Q28588551 |
| | Identification of Vangl2 and Scrb1 as planar polarity genes in mammals | Q28593071 |
| | PDZ Domain Proteins: Plug and Play! | Q30164767 |
| | In utero meconium exposure increases spinal cord necrosis in a rat model of myelomeningocele | Q30823458 |
| | Proteomic analysis of amniotic fluid in pregnancies with Down syndrome | Q33250496 |
| | Proteomics analysis of human coronary atherosclerotic plaque: a feasibility study of direct tissue proteomics by liquid chromatography and tandem mass spectrometry | Q33276995 |
| | Fetal alcohol syndrome (FAS) in C57BL/6 mice detected through proteomics screening of the amniotic fluid | Q33317779 |
| | Neural tube defects--disorders of neurulation and related embryonic processes | Q33620903 |
| | Neural tube defects: recent advances, unsolved questions, and controversies | Q33620909 |
| | Neural-tube defects | Q33772419 |
| | Novel mutations in VANGL1 in neural tube defects | Q33912301 |
| | SELDI-TOF-MS proteomic profiling of serum, urine, and amniotic fluid in neural tube defects | Q33940289 |
| | Cats, frogs, and snakes: early concepts of neural tube defects | Q33951478 |
| | Comparative proteomics of spinal cords of rat fetuses with spina bifida aperta | Q34030059 |
| | A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? | Q34385362 |
| | From proteins to proteomes: large scale protein identification by two-dimensional electrophoresis and amino acid analysis | Q34472916 |
| | Folic acid supplementation in pregnancy and implications in health and disease | Q34544563 |
| | Vitamin deficiencies and neural tube defects | Q34989467 |
| | Epidemiology of neural tube defects | Q35147172 |
| | Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. | Q35196427 |
| | Cell polarity pathways converge and extend to regulate neural tube closure. | Q35208566 |
| | Dishevelled: linking convergent extension with neural tube closure | Q35209196 |
| | The genetic basis of mammalian neurulation. | Q35298412 |
| | Prenatal screening, diagnosis, and pregnancy management of fetal neural tube defects | Q35399092 |
| | Economic burden of neural tube defects and impact of prevention with folic acid: a literature review | Q35402500 |
| | The role of cysteine residues as redox-sensitive regulatory switches | Q35975035 |
| | A protein complex of SCRIB, NOS1AP and VANGL1 regulates cell polarity and migration, and is associated with breast cancer progression. | Q36166916 |
| | The role of proteomics in the assessment of premature rupture of fetal membranes. | Q36170023 |
| | Planar cell polarization: an emerging model points in the right direction | Q36280306 |
| | Etiology, pathogenesis and prevention of neural tube defects | Q36491874 |
| | Noncanonical Wnt signaling and neural polarity | Q36507595 |
| | Neural tube defects induced by folate deficiency in mutant curly tail (Grhl3) embryos are associated with alteration in folate one-carbon metabolism but are unlikely to result from diminished methylation | Q36789456 |
| | Content of a complete routine second trimester obstetrical ultrasound examination and report | Q37470953 |
| | Convergence and extension movements during vertebrate gastrulation | Q37593745 |
| | An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure | Q37782587 |
| | The prevalence of congenital anomalies in Europe | Q37786255 |
| | The planar cell polarity pathway in vertebrate epidermal development, homeostasis and repair | Q37951269 |
| | A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects | Q38048237 |
| | Expanding the mutational spectrum associated to neural tube defects: literature revision and description of novel VANGL1 mutations. | Q38248134 |
| | The human PDZome: a gateway to PSD95-Disc large-zonula occludens (PDZ)-mediated functions | Q39145697 |
| | Exosomes mediate stromal mobilization of autocrine Wnt-PCP signaling in breast cancer cell migration. | Q39222362 |
| | Metabonomic profiling of human placentas reveals different metabolic patterns among subtypes of neural tube defects | Q39278144 |
| | Neural tube defects in curly-tail mice. I. Incidence, expression and similarity to the human condition | Q39289567 |
| | Characterization of sugar chain structures of human alpha-fetoprotein by lectin affinity electrophoresis. ibarahp@oka.urban.ne.jp | Q39481752 |
| | The cell polarity PTK7 receptor acts as a modulator of the chemotherapeutic response in acute myeloid leukemia and impairs clinical outcome | Q39691348 |
| | Causation of neural tube defects: clues from epidemiology | Q39953969 |
| | Advent of maternal serum markers for Down syndrome screening. | Q40401712 |
| | Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide | Q41811946 |
| | The effectiveness of prenatal serum biomarker screening for neural tube defects in second trimester pregnant women: a meta-analysis | Q43809359 |
| | Maternal serum triple analyte screening in pregnancy. | Q43920543 |
| | MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect | Q44367174 |
| | dishevelled is required during wingless signaling to establish both cell polarity and cell identity. | Q46120418 |
| | Routine ultrasonography compared with maternal serum alpha-fetoprotein for neural tube defect screening. | Q46303467 |
| | Neural tube defects and disturbed maternal folate- and homocysteine-mediated one-carbon metabolism | Q46511283 |
| | Spontaneous neural tube defects in splotch mice supplemented with selected micronutrients. | Q46754696 |
| | Predicting protein homocysteinylation targets based on dihedral strain energy and pKa of cysteines | Q46853504 |
| | The Drosophila tissue polarity gene starry night encodes a member of the protocadherin family | Q47072686 |
| | Amniotic fluid and serum biomarkers from women with neural tube defect-affected pregnancies: a case study for myelomeningocele and anencephaly: clinical article | Q47716936 |
| | Embryonic folate metabolism and mouse neural tube defects | Q47923879 |
| | Multiple neural tube defects may not be very rare. | Q50891555 |
| | Elevated rates of severe neural tube defects in a high-prevalence area in northern China. | Q52191680 |
| | Metabolic signature of pregnant women with neural tube defects in offspring. | Q52616079 |
| | Analyzing planar cell polarity during zebrafish gastrulation. | Q52620199 |
| | Multiple alpha-fetoprotein RNAs in adult rat liver: cell type-specific expression and differential regulation | Q53496823 |
| | The planar cell polarity pathway drives pathogenesis of chronic lymphocytic leukemia by the regulation of B-lymphocyte migration. | Q54455172 |
| | VANGL2 mutations in human cranial neural-tube defects | Q55671436 |
| | Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects | Q57677677 |
| | Proteomic analysis of human vessels: Application to atherosclerotic plaques | Q59315364 |
| | Expression of the Notch 3 intracellular domain in mouse central nervous system progenitor cells is lethal and leads to disturbed neural tube development | Q62003158 |
| | Reactivity of amniotic fluid alpha-fetoprotein with concanavallin A in diagnosis of neural tube defects | Q66702772 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P304 | page(s) | 164-183 | |
| P577 | publication date | 2015-03-17 | |
| P1433 | published in | Metabolites | Q27724046 |
| P1476 | title | Neural tube defects: from a proteomic standpoint | |
| P478 | volume | 5 | |