about
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseVangl-dependent planar cell polarity signalling is not required for neural crest migration in mammals.Convergent extension analysis in mouse whole embryo cultureGene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function.Apoptosis is not required for mammalian neural tube closure.Cornelia de Lange Syndrome: NIPBL haploinsufficiency downregulates canonical Wnt pathway in zebrafish embryos and patients fibroblasts.Understanding the causes and prevention of neural tube defects: Insights from the splotch mouse model.Use of high-frequency ultrasound to study the prenatal development of cranial neural tube defects and hydrocephalus in Gldc-deficient miceInflammation modulates LC3 expression in human preterm delivery.Effects of excess and deprivation of serotonin on in vitro neuronal differentiation.Foregut separation and tracheo-oesophageal malformations: the role of tracheal outgrowth, dorso-ventral patterning and programmed cell death.Relationship between hindbrain segmentation, neural crest cell migration and branchial arch abnormalities in rat embryos exposed to fluconazole and retinoic acid in vitro.Craniofacial and axial skeletal defects induced by the fungicide triadimefon in the mouse.Study on the common teratogenic pathway elicited by the fungicides triazole-derivatives.Inhibition of histone deacetylase activity on specific embryonic tissues as a new mechanism for teratogenicity.Myo-inositol enhances teratogenicity of valproic acid in the mouse.CyclinD1 Down-Regulation and Increased Apoptosis Are Common Features of Cohesinopathies.Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome.Rings and Bricks: Expression of Cohesin Components is Dynamic during Development and Adult Life.Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngioma.Re: Clinical interventions to reduce stillbirths in sub-Saharan Africa: a mathematical model to estimate the potential reduction of stillbirths associated with specific obstetric conditions: Nuchal cord and stillbirths: true or false myth?Krox20 is down-regulated following triazole in vitro embryonic exposure: a polycompetitor-based assay.Impairment of Retinoic Acid Signaling in Cornelia de Lange Syndrome FibroblastsCornelia de Lange syndrome: To diagnose or not to diagnose in utero?Overview on neural tube defects: From development to physical characteristicsFetal pancreatic Langerhans islets size in pregnancies with metabolic disordersGestational diabetes affects fetal autophagyCell death and cell proliferation in human spina bifidaCellular mechanisms underlying Pax3-related neural tube defects and their prevention by folic acidChromatinopathies: A focus on Cornelia de Lange syndromeDynamic acetylation profile during mammalian neurulationThe Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genesFirst evidence of a paediatric patient with Cornelia de Lange syndrome with acute lymphoblastic leukaemia
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Valentina Massa
@ast
Valentina Massa
@en
Valentina Massa
@es
Valentina Massa
@nl
Valentina Massa
@sl
type
label
Valentina Massa
@ast
Valentina Massa
@en
Valentina Massa
@es
Valentina Massa
@nl
Valentina Massa
@sl
prefLabel
Valentina Massa
@ast
Valentina Massa
@en
Valentina Massa
@es
Valentina Massa
@nl
Valentina Massa
@sl
P1053
A-6081-2014
P106
P1153
6701628384
P21
P31
P3829
P496
0000-0003-2246-9515