Search Results - "Wert, S."
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1
Hippocampus-dependent memory and allele-specific gene expression in adult offspring of alcohol-consuming dams after neonatal treatment with thyroxin or metformin
Published in Molecular psychiatry (01-07-2018)“…Fetal alcohol spectrum disorder (FASD), the result of fetal alcohol exposure (FAE), affects 2–11% of children worldwide, with no effective treatments…”
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2
Pilot validation of blood-based biomarkers during pregnancy and postpartum in women with prior or current depression
Published in Translational psychiatry (21-01-2021)“…Major depressive disorder (MDD) is more common in women than in men, and evidence of gender-related subtypes of depression is emerging. Previously identified…”
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3
Genetic stress-reactivity, sex, and conditioning intensity affect stress-enhanced fear learning
Published in Neurobiology of learning and memory (01-11-2021)“…•Stress-Enhanced Fear Learning and fear memory modified by genetic stress-sensitivity.•Stress-Enhanced Fear Learning and fear memory are highly…”
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4
Heterogeneous stock rats: a model to study the genetics of despair‐like behavior in adolescence
Published in Genes, brain and behavior (01-02-2018)“…Major depressive disorder (MDD) is a complex illness caused by both genetic and environmental factors. Antidepressant resistance also has a genetic component…”
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5
Nature and nurture: environmental influences on a genetic rat model of depression
Published in Translational psychiatry (29-03-2016)“…In this study, we sought to learn whether adverse events such as chronic restraint stress (CRS), or ‘nurture’ in the form of environmental enrichment (EE),…”
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6
Stage-specific regulation of respiratory epithelial cell differentiation by Foxa1
Published in American journal of physiology. Lung cellular and molecular physiology (01-11-2005)“…Foxa1 is a member of the winged helix family of transcription factors that is expressed in epithelial cells of the conducting airways and in alveolar type II…”
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7
Ectopic respiratory epithelial cell differentiation in bronchiolised distal airspaces in idiopathic pulmonary fibrosis
Published in Thorax (01-08-2011)“…Bronchiolisation of distal airspaces is an unexplained feature of idiopathic pulmonary fibrosis (IPF). The authors sought to identify mechanisms driving the…”
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8
Allelic Heterogeneity in Hereditary Surfactant Protein B (SP-B) Deficiency
Published in American journal of respiratory and critical care medicine (01-03-2000)“…Inability to produce surfactant protein B (SP-B) causes fatal neonatal respiratory disease. A frame-shift mutation (121ins2) is the predominant but not…”
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A Mutation in the Surfactant Protein C Gene Associated with Familial Interstitial Lung Disease
Published in The New England journal of medicine (22-02-2001)“…Interstitial lung diseases are a heterogeneous group of disorders that are poorly understood at a molecular level. 1 , 2 The cause is often unknown, and the…”
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10
Targeted expression of a dominant negative FGF receptor blocks branching morphogenesis and epithelial differentiation of the mouse lung
Published in The EMBO journal (15-07-1994)“…Mouse lung development begins when two lung buds sprout from the epithelium of the embryonic gut. Patterning of the airways is then accomplished by the…”
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11
Targeted disruption of the surfactant protein B gene disrupts surfactant homeostasis, causing respiratory failure in newborn mice
Published in Proceedings of the National Academy of Sciences - PNAS (15-08-1995)“…Surfactant protein B (SP-B) is an 8.7-kDa, hydrophobic protein that enhances the spreading and stability of surfactant phospholipids in the alveolus. To…”
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12
Tissue-specific regulation of the alpha-myosin heavy chain gene promoter in transgenic mice
Published in The Journal of biological chemistry (25-12-1991)“…The intergenic region between the mouse alpha-myosin heavy chain (MHC) and beta-MHC genes was analyzed in terms of its ability to drive gene expression in…”
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13
Altered Surfactant Function and Structure in SP-A Gene Targeted Mice
Published in Proceedings of the National Academy of Sciences - PNAS (03-09-1996)“…The surfactant protein A (SP-A) gene was disrupted by homologous recombination in embryonic stem cells that were used to generate homozygous SP-A-deficient…”
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14
Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutation
Published in Pediatric research (01-09-2000)“…Hereditary surfactant protein B (SP-B) deficiency has been lethal in the first year of life without lung transplantation. We tested the hypothesis that SP-B…”
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15
Increased Metalloproteinase Activity, Oxidant Production, and Emphysema in Surfactant Protein D Gene-Inactivated Mice
Published in Proceedings of the National Academy of Sciences - PNAS (23-05-2000)“…Targeted ablation of the surfactant protein D (SP-D) gene caused chronic inflammation, emphysema, and fibrosis in the lungs of SP-D (-/-) mice. Although lung…”
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16
Transcriptional Elements from the Human SP-C Gene Direct Expression in the Primordial Respiratory Epithelium of Transgenic Mice
Published in Developmental biology (01-04-1993)“…Transgenic animals bearing a chimeric gene containing 5′-flanking regions of the human surfactant protein C (SPC) gene ligated to the bacterial chloramphenicol…”
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Correction of Lethal Intestinal Defect in a Mouse Model of Cystic Fibrosis by Human CFTR
Published in Science (American Association for the Advancement of Science) (09-12-1994)“…Cystic fibrosis (CF) is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR). A potential animal model of…”
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18
Hepatocyte nuclear factor 3 activates transcription of thyroid transcription factor 1 in respiratory epithelial cells
Published in Molecular and Cellular Biology (01-07-1996)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Pulmonary Malformation in Transgenic Mice Expressing Human Keratinocyte Growth Factor in the Lung
Published in Proceedings of the National Academy of Sciences - PNAS (19-12-1995)“…Expression of human keratinocyte growth factor (KGF/FGF-7) was directed to epithelial cells of the developing embryonic lung of transgenic mice disrupting…”
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20
Deficiency of lamellar bodies in alveolar type II cells associated with fatal respiratory disease in a full-term infant
Published in American journal of respiratory and critical care medicine (01-02-2000)“…We report a case of a full-term female infant who presented with severe respiratory distress shortly after birth and died at 23 d of age with unremitting…”
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