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Contribution of VANGL2 mutations to isolated neural tube defects

Clinical genetics, 2011-07, Vol.80 (1), p.76-82

2011

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Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations

Birth defects research. A Clinical and molecular teratology, 2015-01, Vol.103 (1), p.51-61

2015

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Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Journal of human genetics, 2002-06, Vol.47 (6), p.319-324

2002

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Induction of Macrophage Glutamine: Fructose-6-Phosphate Amidotransferase Expression by Hypoxia and by Picolinic Acid

International journal of immunopathology and pharmacology, 2007-01, Vol.20 (1), p.47-58

2007

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Successful isolation and long-term establishment of a cell line with stem cell-like features from an anaplastic medulloblastoma

Neuropathology and applied neurobiology, 2008-06, Vol.34 (3), p.306-315

2008

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Mutations in VANGL1 Associated with Neural-Tube Defects

The New England journal of medicine, 2007-04, Vol.356 (14), p.1432-1437

2007

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Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans

Human molecular genetics, 2011-11, Vol.20 (22), p.4324-4333

2011

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La grâce de montrer son âme dans le vêtement » Scrivere di tessuti, abiti, accessori. Studi in onore di Liana Nissim: (TOMO II) - L'Ottocento e il Tournant du Siecle

2015

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Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans

Human molecular genetics, 2015-07, Vol.24 (13), p.3893-3893

2015

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Hypoxia transcriptionally induces macrophage-inflammatory protein-3α/CCL-20 in primary human mononuclear phagocytes through nuclear factor (NF)-κB

Journal of leukocyte biology, 2008-03, Vol.83 (3), p.648-662

2008

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Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway

Human molecular genetics, 2014-08, Vol.23 (15), p.4185-4185

2014

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Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk

Journal of human genetics, 2006-02, Vol.51 (2), p.98-103

2006

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Reduced folate carrier polymorphism (80A→G) and neural tube defects

European journal of human genetics : EJHG, 2003-03, Vol.11 (3), p.245-252

2003

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On the lifespan of classical solutions to a non-local porous medium problem with nonlinear boundary conditions

Discrete and continuous dynamical systems. Series S, 2020-07, Vol.13 (7), p.2033-2045

2020

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A note on a class of 4th order hyperbolic problems with weak and strong damping and superlinear source term

Discrete and continuous dynamical systems. Series S, 2020-07, Vol.13 (7), p.2047-2055

2020

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Decay in chemotaxis systems with a logistic term

Discrete and continuous dynamical systems. Series S, 2020-02, Vol.13 (2), p.257-268

2020

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Blow-up phenomena for nonlinear pseudo-parabolic equations with gradient term

Discrete and continuous dynamical systems. Series B, 2017-08, Vol.22 (6), p.2291-2300

2017

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Polymorphisms in Genes Involved in Folate Metabolism as Risk Factors for NTDs

European journal of pediatric surgery, 2001-12, Vol.11 (S1), p.S14-S17

2001

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HLXB9 homeobox gene and caudal regression syndrome

Birth defects research. A Clinical and molecular teratology, 2006-03, Vol.76 (3), p.205-209

2006

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Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome

Birth defects research. A Clinical and molecular teratology, 2006-02, Vol.76 (2), p.86-95

2006

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Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defects

Birth defects research. A Clinical and molecular teratology, 2004-11, Vol.70 (11), p.885-888

2004

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Methylenetetrahydrofolate-dehydrogenase 1958G→A polymorphism is a genetic determinant of NTD risk for Italian mothers

Cerebrospinal fluid research, 2004-12, Vol.1 (S1), p.S50-S50, Article S50

2004

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Existence and convexity of solutions of the fractional heat equation

Communications on pure and applied analysis, 2017-11, Vol.16 (6), p.2201-2226

2017

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Folate pathway gene alterations in patients with neural tube defects

American journal of medical genetics, 2000-11, Vol.95 (3), p.216-223

2000

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Testing the Larson relations in massive clumps

Monthly notices of the Royal Astronomical Society, 2018-06, Vol.477 (2), p.2220-2242

2018

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Contribution of VANGL2 mutations to isolated neural tube defects

Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Induction of Macrophage Glutamine: Fructose-6-Phosphate Amidotransferase Expression by Hypoxia and by Picolinic Acid

Successful isolation and long-term establishment of a cell line with stem cell-like features from an anaplastic medulloblastoma

Mutations in VANGL1 Associated with Neural-Tube Defects

Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans

La grâce de montrer son âme dans le vêtement » Scrivere di tessuti, abiti, accessori. Studi in onore di Liana Nissim: (TOMO II) - L'Ottocento e il Tournant du Siecle

Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans

Hypoxia transcriptionally induces macrophage-inflammatory protein-3α/CCL-20 in primary human mononuclear phagocytes through nuclear factor (NF)-κB

Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway

Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk

Reduced folate carrier polymorphism (80A→G) and neural tube defects

On the lifespan of classical solutions to a non-local porous medium problem with nonlinear boundary conditions

A note on a class of 4th order hyperbolic problems with weak and strong damping and superlinear source term

Decay in chemotaxis systems with a logistic term

Blow-up phenomena for nonlinear pseudo-parabolic equations with gradient term

Polymorphisms in Genes Involved in Folate Metabolism as Risk Factors for NTDs

HLXB9 homeobox gene and caudal regression syndrome

Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome

Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defects

Methylenetetrahydrofolate-dehydrogenase 1958G→A polymorphism is a genetic determinant of NTD risk for Italian mothers

Existence and convexity of solutions of the fractional heat equation

Folate pathway gene alterations in patients with neural tube defects

Testing the Larson relations in massive clumps

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