Search Results - "GERMAIN, L"
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1
Alterations in sperm long RNA contribute to the epigenetic inheritance of the effects of postnatal trauma
Published in Molecular psychiatry (01-09-2020)“…Psychiatric diseases have a strong heritable component known to not be restricted to DNA sequence-based genetic inheritance alone but to also involve…”
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2
An advanced approach to reconstructing parent orientation maps in the case of approximate orientation relations: Application to steels
Published in Acta materialia (01-06-2012)“…Reconstructions allow the evaluation of the microtexture before phase transformation from that measured by EBSD after phase transformation. Even though they…”
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3
Deep Learning for automated phase segmentation in EBSD maps. A case study in Dual Phase steel microstructures
Published in Materials characterization (01-02-2022)“…Electron Backscattering Diffraction (EBSD) provides important information to discriminate phase transformation products in steels. This task is conventionally…”
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4
Texture and microtexture variations in a near-α titanium forged disk of bimodal microstructure
Published in Acta materialia (01-04-2012)“…Quasi-alpha titanium billets often contain macrozones, i.e. large regions of sharp microtexture that differ from one region to the next and are detrimental for…”
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5
Spherical indexing of overlap EBSD patterns for orientation-related phases – Application to titanium
Published in Acta materialia (15-04-2020)“…[Display omitted] We propose a new electron backscatter diffraction (EBSD) indexing approach that can handle overlapping patterns arising from fine-scale…”
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6
Single dose moxidectin versus ivermectin for Onchocerca volvulus infection in Ghana, Liberia, and the Democratic Republic of the Congo: a randomised, controlled, double-blind phase 3 trial
Published in The Lancet (British edition) (06-10-2018)“…The morbidity and socioeconomic effects of onchocerciasis, a parasitic disease that is primarily endemic in sub-Saharan Africa, have motivated large morbidity…”
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7
Targeting myostatin/activin A protects against skeletal muscle and bone loss during spaceflight
Published in Proceedings of the National Academy of Sciences - PNAS (22-09-2020)“…Among the physiological consequences of extended spaceflight are loss of skeletal muscle and bone mass. One signaling pathway that plays an important role in…”
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8
Life without Thyroxine to 3,5,3′-Triiodothyronine Conversion: Studies in Mice Devoid of the 5′-Deiodinases
Published in Endocrinology (Philadelphia) (01-06-2009)“…Considerable indirect evidence suggests that the type 2 deiodinase (D2) generates T3 from T4 for local use in specific tissues including pituitary, brown fat,…”
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9
Interactions between ferrite recrystallization and austenite formation in high-strength steels
Published in Journal of materials science (01-05-2014)“…Using both experimental and modeling approaches, we give some clarifications regarding the mechanisms of interaction between ferrite recrystallization and…”
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10
Type 3 Deiodinase Role on Central Thyroid Hormone Action Affects the Leptin-Melanocortin System and Circadian Activity
Published in Endocrinology (Philadelphia) (01-02-2017)“…The role of thyroid hormones (TH) in the central regulation of energy balance is increasingly appreciated. Mice lacking the type 3 deiodinase (DIO3), which…”
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11
Influence of transformation temperature on microtexture formation associated with α precipitation at β grain boundaries in a β metastable titanium alloy
Published in Acta materialia (01-06-2013)“…The influence of transformation temperature on microtexture development associated with α precipitation at β/β grain boundaries (GB) in the near-β Ti17 alloy…”
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12
Type 3 Deiodinase, a Thyroid-Hormone-Inactivating Enzyme, Controls Survival and Maturation of Cone Photoreceptors
Published in The Journal of neuroscience (03-03-2010)“…Maturation of the mammalian nervous system requires adequate provision of thyroid hormone and mechanisms that enhance tissue responses to the hormone. Here, we…”
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13
Autologous bilayered self-assembled skin substitutes (SASSs) as permanent grafts: a case series of 14 severely burned patients indicating clinical effectiveness
Published in European cells & materials (13-09-2018)“…Split-thickness skin autografts (AGs) are the standard surgical treatment for severe burn injuries. However, the treatment of patients with substantial skin…”
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14
A Protective Role for Type 3 Deiodinase, a Thyroid Hormone-Inactivating Enzyme, in Cochlear Development and Auditory Function
Published in Endocrinology (Philadelphia) (01-04-2009)“…Thyroid hormone is necessary for cochlear development and auditory function, but the factors that control these processes are poorly understood. Previous…”
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15
Nitrogen isotope fractionation in amino acids from harbor seals: implications for compound-specific trophic position calculations
Published in Marine ecology. Progress series (Halstenbek) (22-05-2013)“…Compound-specific isotope analysis of individual amino acids (AA) is a rapidly growing tool in ecological studies to assess diet and trophic position (TP) in…”
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16
Adult onset of type 3 deiodinase deficiency in mice alters brain gene expression and increases locomotor activity
Published in Psychoneuroendocrinology (01-12-2019)“…[Display omitted] •Adult-onset deficiency in the type 3 deiodinase (DIO3) leads to increased locomotor activity in females.•Adult loss of DIO3 causes increases…”
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17
Cerebellar Abnormalities in Mice Lacking Type 3 Deiodinase and Partial Reversal of Phenotype by Deletion of Thyroid Hormone Receptor α1
Published in Endocrinology (Philadelphia) (01-01-2013)“…Thyroid hormone serves many functions throughout brain development, but the mechanisms that control the timing of its actions in specific brain regions are…”
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18
Functional redundancy of type I and type II receptors in the regulation of skeletal muscle growth by myostatin and activin A
Published in Proceedings of the National Academy of Sciences - PNAS (08-12-2020)“…Myostatin (MSTN) is a transforming growth factor-β (TGF-β) family member that normally acts to limit muscle growth. The function of MSTN is partially redundant…”
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19
Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development
Published in PloS one (20-01-2023)“…Albright hereditary osteodystrophy (AHO) is caused by heterozygous inactivating mutations in GNAS. Patients with maternally-inherited mutations develop…”
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Type 3 Deiodinase Deficiency Causes Spatial and Temporal Alterations in Brain T3 Signaling that Are Dissociated from Serum Thyroid Hormone Levels
Published in Endocrinology (Philadelphia) (01-11-2010)“…The type 3 deiodinase (D3) is an enzyme that inactivates thyroid hormones (TH) and is highly expressed during development and in the central nervous system…”
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