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The Notch Signalling Pathway in the Development of the Mouse Placenta

Placenta (Eastbourne), 2008-08, Vol.29 (8), p.651-659

2008

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Metabolic scaling law for mouse fetal and placental weight

Placenta (Eastbourne), 2013-11, Vol.34 (11), p.1099-1101

2013

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Mammalian Groucho homologs: Redundancy or specificity?

Journal of cellular biochemistry, 2005-07, Vol.95 (4), p.670-687

2005

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Establishing Three Blastocyst Lineages—Then What?

Biology of reproduction, 2011-04, Vol.84 (4), p.621-630

2011

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Growth Factors and Trophoblast Differentiation – Workshop Report

Placenta, 2007-04, Vol.28, p.S121-S124

2007

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Simplified method for gene targeting vector construction

BioTechniques, 2004-11, Vol.37 (5), p.734-738

2004

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Welcome to Parenthood is associated with reduction of postnatal depressive symptoms during the transition from pregnancy to 6 months postpartum in a community sample: a longitudinal evaluation

Archives of women's mental health, 2021-06, Vol.24 (3), p.493-501

2021

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Association between social relationship of mentors and depressive symptoms in first-time mothers during the transition from pregnancy to 6-months postpartum

Maternal health, neonatology and perinatology, 2024-02, Vol.10 (1), p.4-4, Article 4

2024

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A role for Notch signaling in trophoblast endovascular invasion and in the pathogenesis of pre-eclampsia

Development (Cambridge), 2011-07, Vol.138 (14), p.2987-2998

2011

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DNA methylation in ELOVL2 and C1orf132 correctly predicted chronological age of individuals from three disease groups

International journal of legal medicine, 2018-01, Vol.132 (1), p.1-11

2018

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Mosaic IL6ST variant inducing constitutive GP130 cytokine receptor signaling as a cause of neonatal onset immunodeficiency with autoinflammation and dysmorphy

Human molecular genetics, 2021-04, Vol.30 (3-4), p.226-233

2021

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Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia

Human molecular genetics, 2018-11, Vol.27 (21), p.3669-3674

2018

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A de novo loss‐of‐function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa

Clinical genetics, 2018-05, Vol.93 (5), p.1107-1108

2018

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Covid-19: An urgent call for global "vaccines-plus" action

BMJ (Online), 2022-01, Vol.376, p.o1

2022

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Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit

Journal of clinical medicine, 2020-07, Vol.9 (7), p.2220

2020

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Novel Loss of Function Variants in ICENPF/I Including a Large Intragenic Deletion in Patients with Strømme Syndrome

Genes, 2023-10, Vol.14 (11)

2023

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Broad clinical spectrum observed in patients with scapuloperoneal spinal muscular atrophy (SPSMA) caused by an c.806G > A (p. Arg269His) mutation in the TRPV4 gene

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S135

2017

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P.128 - Broad clinical spectrum observed in patients with scapuloperoneal spinal muscular atrophy (SPSMA) caused by an c.806G > A (p. Arg269His) mutation in the TRPV4 gene

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S135-S135

2017

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Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome

Genes, 2023-10, Vol.14 (11), p.1985

2023

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A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy - a case report and review of the genotype-phenotype correlation

Folia neuropathologica, 2017-01, Vol.55 (3), p.214-220

2017

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DNA methylation signature in blood does not predict calendar age in patients with chronic lymphocytic leukemia but may alert to the presence of disease

Forensic science international : genetics, 2018-05, Vol.34, p.e15-e17

2018

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Grafting of styrene onto poly(butyl acrylate) in emulsion

Polymer (Guilford), 1982-01, Vol.23 (6), p.839-842

1982

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The Notch Signalling Pathway in the Development of the Mouse Placenta

Metabolic scaling law for mouse fetal and placental weight

IFPA Meeting 2011 workshop report II: Angiogenic signaling and regulation of fetal endothelial function; placental and fetal circulation and growth; spiral artery remodeling

Mammalian Groucho homologs: Redundancy or specificity?

Establishing Three Blastocyst Lineages—Then What?

Growth Factors and Trophoblast Differentiation – Workshop Report

IFPA Meeting 2011 workshops report II: Angiogenic signaling and regulation of fetal endothelial function; placental and fetal circulation and growth; spiral artery remodeling: Placenta - Predicting Future Health

Simplified method for gene targeting vector construction

Welcome to Parenthood is associated with reduction of postnatal depressive symptoms during the transition from pregnancy to 6 months postpartum in a community sample: a longitudinal evaluation

Association between social relationship of mentors and depressive symptoms in first-time mothers during the transition from pregnancy to 6-months postpartum

A role for Notch signaling in trophoblast endovascular invasion and in the pathogenesis of pre-eclampsia

DNA methylation in ELOVL2 and C1orf132 correctly predicted chronological age of individuals from three disease groups

Mosaic IL6ST variant inducing constitutive GP130 cytokine receptor signaling as a cause of neonatal onset immunodeficiency with autoinflammation and dysmorphy

Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia

A de novo loss‐of‐function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa

Covid-19: An urgent call for global "vaccines-plus" action

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit

Novel Loss of Function Variants in ICENPF/I Including a Large Intragenic Deletion in Patients with Strømme Syndrome

Broad clinical spectrum observed in patients with scapuloperoneal spinal muscular atrophy (SPSMA) caused by an c.806G > A (p. Arg269His) mutation in the TRPV4 gene

P.128 - Broad clinical spectrum observed in patients with scapuloperoneal spinal muscular atrophy (SPSMA) caused by an c.806G > A (p. Arg269His) mutation in the TRPV4 gene

Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome

A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy - a case report and review of the genotype-phenotype correlation

DNA methylation signature in blood does not predict calendar age in patients with chronic lymphocytic leukemia but may alert to the presence of disease

Grafting of styrene onto poly(butyl acrylate) in emulsion

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