Search Results - "Morissette, Rachel"
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Trends in ingredients added to infant formula: FDA's experiences in the GRAS notification program
Published in Food and chemical toxicology (01-08-2023)“…While human milk is considered the optimal source of nutrition for infants for the first six and twelve months of age, with continued benefit of breastfeeding…”
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Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians
Published in Genetics in medicine (01-11-2017)“…Purpose Nonclassic 21-hydroxylase deficiency, a mild form of congenital adrenal hyperplasia (CAH), is estimated to be the most common autosomal recessive…”
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3
sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Published in Nature (London) (14-04-2016)“…Aged fibroblasts release a Wnt antagonist, sFRP2, which drives a signalling cascade in melanoma cells, leading to increased metastasis and reduced…”
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4
Science surrounding the safe use of bioactive ingredients in infant formula: federal comment
Published in Pediatric research (01-08-2023)“…Less than a quarter of U.S. infants meet the federal recommendation for exclusively breastfeeding to 6 months of age, necessitating access to safe and…”
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Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal Hyperplasia
Published in Human mutation (01-09-2016)“…ABSTRACT Some variants that cause autosomal‐recessive congenital adrenal hyperplasia (CAH) also cause hypermobility type Ehlers–Danlos syndrome (EDS) due to…”
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Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia
Published in The journal of clinical endocrinology and metabolism (01-08-2015)“…Context: The contiguous gene deletion syndrome (CAH-X) was described in a subset (7%) of congenital adrenal hyperplasia (CAH) patients with a TNXA/TNXB…”
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Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF‐β expression and connective tissue features
Published in The FASEB journal (01-08-2014)“…Fibromuscular dysplasia (FMD) is a rare, nonatherosclerotic arterial disease for which the molecular basis is unknown. We comprehensively studied 47 subjects…”
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The soluble domains of Gpi8 and Gaa1, two subunits of glycosylphosphatidylinositol transamidase (GPI-T), assemble into a complex
Published in Archives of biochemistry and biophysics (01-11-2017)“…Glycosylphosphatidylinositol transamidase (GPI-T) catalyzes the post-translational addition of the GPI anchor to the C-terminus of some proteins. In most…”
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A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with marfan and loeys-dietz syndrome
Published in American journal of medical genetics. Part A (01-08-2013)“…The transforming growth factor β (TGF‐β) family of growth factors are key regulators of mammalian development and their dysregulation is implicated in human…”
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Tenascin-X Haploinsufficiency Associated with Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia
Published in The journal of clinical endocrinology and metabolism (01-02-2013)“…Context: The gene for congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, CYP21A2, is flanked by the gene encoding tenascin-X (TNXB), a…”
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Transforming growth factor-β (TGF-β) pathway abnormalities in tenascin-X deficiency associated with CAH-X syndrome
Published in European journal of medical genetics (01-02-2014)“…Abstract Patients with congenital adrenal hyperplasia (CAH) with tenascin-X deficiency (CAH-X syndrome) have both endocrine imbalances and characteristic…”
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Tenascin-X gene defects and cardiovascular disease
Published in Medical hypotheses (01-12-2014)Get full text
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13
Transforming Growth Factor-β and Inflammation in Vascular (Type IV) Ehlers–Danlos Syndrome
Published in Circulation. Cardiovascular genetics (01-02-2014)“…BACKGROUND—Vascular Ehlers–Danlos syndrome (VEDS) causes reduced life expectancy because of arterial dissections/rupture and hollow organ rupture. Although the…”
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Abstract A04: Aging microenvironment modulates melanoma invasion and metastasis
Published in Cancer research (Chicago, Ill.) (15-07-2015)“…Abstract The incidence of melanoma rises dramatically after the age of 55. Due to an increase in aging population, it is important to study the change in…”
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Erratum: Corrigendum: sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Published in Nature (London) (06-07-2016)Get full text
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Corrigendum: sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Published in Nature (London) (08-09-2016)Get full text
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Correction: Corrigendum: sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Published in Nature (London) (01-09-2016)“…Nature 532, 250–254 (2016); doi:10.1038/nature17392 In Fig. 5a of this Letter, the labels PBS and PLX4720 were inadvertently reversed. The corrected Fig. 5a is…”
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Defining the boundaries of species specificity for the Saccharomyces cerevisiae glycosylphosphatidylinositol transamidase using a quantitative in vivo assay
Published in Bioscience reports (01-12-2012)“…In eukaryotes, GPI (glycosylphosphatidylinositol) lipid anchoring of proteins is an abundant post-translational modification. The attachment of the GPI anchor…”
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A mutation in TGFB 3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with marfan and loeys–dietz syndrome
Published in American journal of medical genetics. Part A (01-08-2013)“…Abstract The transforming growth factor β (TGF‐β) family of growth factors are key regulators of mammalian development and their dysregulation is implicated in…”
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Methods to characterize and assay the Saccharomyces cerevisiae GPI transamidase - A membrane-bound, multi-subunit enzyme that post-translationally modifies proteins
Published 01-01-2008“…Post-translational modification of proteins is a common event which increases the diversity of chemical groups available to enhance protein function. One of…”
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