Search Results - "Clemessy, Maud"
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Stimulation of GHRH Neuron Axon Growth by Leptin and Impact of Nutrition during Suckling in Mice
Published in Nutrients (21-02-2023)“…Nutrition during the early postnatal period can program the growth trajectory and adult size. Nutritionally regulated hormones are strongly suspected to be…”
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IGF-1 Induces GHRH Neuronal Axon Elongation during Early Postnatal Life in Mice
Published in PloS one (11-01-2017)“…Nutrition during the perinatal period programs body growth. Growth hormone (GH) secretion from the pituitary regulates body growth and is controlled by Growth…”
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Impact of insulin on primary arcuate neurons culture is dependent on early-postnatal nutritional status and neuronal subpopulation
Published in PloS one (21-02-2018)“…Nutrition plays a critical role in programming and shaping linear growth during early postnatal life through direct action on the development of the…”
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4
Knockout of insulin-like growth factor-1 receptor impairs distal lung morphogenesis
Published in PloS one (06-11-2012)“…Insulin-like growth factors (IGF-I and -II) are pleiotropic regulators of somatic growth and development in vertebrate species. Endocrine and paracrine effects…”
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5
Angiopoietin 2 alters pancreatic vascularization in diabetic conditions
Published in PloS one (17-01-2012)“…Islet vascularization, by controlling beta-cell mass expansion in response to increased insulin demand, is implicated in the progression to glucose intolerance…”
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6
Changes in circulating miRNA19a-3p precede insulin resistance programmed by intra-uterine growth retardation in mice
Published in Molecular metabolism (Germany) (01-12-2020)“…Individuals born with intrauterine growth retardation (IUGR) are more prone to cardio-metabolic diseases as adults, and environmental changes during the…”
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Correction: IGF-1 Induces GHRH Neuronal Axon Elongation during Early Postnatal Life in Mice
Published in PloS one (21-02-2017)“…[This corrects the article DOI: 10.1371/journal.pone.0170083.]…”
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Targeted Skin Overexpression of the Mineralocorticoid Receptor in Mice Causes Epidermal Atrophy, Premature Skin Barrier Formation, Eye Abnormalities, and Alopecia
Published in The American journal of pathology (01-09-2007)“…The mineralocorticoid receptor (MR) is a transcription factor of the nuclear receptor family, activation of which by aldosterone enhances salt reabsorption in…”
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Conditional Transgenic Mice for Studying the Role of the Glucocorticoid Receptor in the Renal Collecting Duct
Published in Endocrinology (Philadelphia) (01-05-2009)“…The mineralocorticoid receptor (MR) is a major regulator of renal sodium reabsorption and body fluid homeostasis. However, little is known about glucocorticoid…”
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10
A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosis
Published in Biology open (15-05-2015)“…The enteric nervous system originates from neural crest cells that migrate in chains as they colonize the embryonic gut, eventually forming the myenteric and…”
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11
Cardiovascular Expression of the Mouse WNK1 Gene during Development and Adulthood Revealed by a BAC Reporter Assay
Published in The American journal of pathology (01-07-2006)“…Large deletions in WNK1 are associated with inherited arterial hypertension. WNK1 encodes two types of protein: a kidney-specific isoform (KS-WNK1) lacking…”
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12
Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure
Published in American journal of human genetics (14-08-2009)“…Through linkage analysis and candidate gene sequencing, we identified three unrelated families with the autosomal-dominant inheritance of early onset anemia,…”
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13
Regulation of growth: Epigenetic mechanisms?
Published in Annales d'endocrinologie (01-06-2017)“…Abstract Organism development is controlled by both genetic programs and the environment to insure a reproductive success as adults. Linear growth is an…”
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14
Angiotensinogen Delays Angiogenesis and Tumor Growth of Hepatocarcinoma in Transgenic Mice
Published in Cancer research (Chicago, Ill.) (01-04-2009)“…Angiotensinogen, a member of the serpin family, is involved in the suppression of tumor growth and metastasis. To investigate whether human angiotensinogen…”
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Deletion of WNK1 First Intron Results in Misregulation of Both Isoforms in Renal and Extrarenal Tissues
Published in Hypertension (Dallas, Tex. 1979) (01-12-2008)“…Large deletions in intron 1 of the with-no-lysine kinase type 1 (WNK1) gene cause familial hyperkalemic hypertension. Alternative promoters generate…”
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16
Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking
Published in Human molecular genetics (15-01-2011)“…Renal tubular dysgenesis (RTD) is a recessive autosomal disease characterized by persistent fetal anuria and perinatal death. During the systematic screening…”
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Enhanced expression of ephrins and thrombospondins in the dermis of patients with early diffuse systemic sclerosis: potential contribution to perturbed angiogenesis and fibrosis
Published in Rheumatology (Oxford, England) (01-08-2011)“…Objective. To determine the skin and fibroblast expression of ephrins (EphB4 and EphrinB2) and thrombospondins (TSPs: TSP1 and TSP2) in patients with SSc…”
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Expression of dual angiogenic/neurogenic growth factors in human primary brain tumors
Published in Journal of neuro-oncology (01-03-2012)“…Brain tumors, benign or malignant, are characterized by a very high degree of vascularization. Recent accumulating evidence suggests that during development…”
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Clinical and biochemical characteristics of normotensive patients with primary aldosteronism: a comparison with hypertensive cases
Published in Clinical endocrinology (Oxford) (01-07-2008)“…Summary Objective It is unknown why some patients with biochemical evidence of primary aldosteronism (PA) do not develop hypertension. We aimed to compare…”
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20
Dominant Renin Gene Mutations Associated with Early-On set Hyperuricemia, Anemia, and Chronic Kidney Failure
Published in American journal of human genetics (14-08-2009)“…Through linkage analysis and candidate gene sequencing, we identified three the autosomal-dominant inheritance of early onset anemia, hypouricosuric…”
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