Results 71 to 80 of about 57,538 (217)
The vitamin D receptor (VDR) regulates hair follicle biology through ligand‐dependent and ligand‐independent mechanisms by heterodimerizing with retinoid X receptor, recruiting coactivator complexes, and activating target genes including Wnt inhibitors, hair keratins, and cell cycle regulators.
Liancheng Guan +8 more
wiley +1 more source
Rickets is produced in rats by feeding exclusively with cereals and yellow peas. Whereas feeding with polished rice results in typical rickets, feeding with rice-starch alone will only produce osteoporosis. This difference is not attributable to nitrogen starvation.If oatmeal is extracted with hydrochloric acid and the extract is given in addition to ...
openaire +2 more sources
ABSTRACT Background and Aims Vitamin D deficiency in pregnancy has been linked to adverse maternal and neonatal outcomes, but evidence from Uganda is limited. We estimated the prevalence of maternal vitamin D deficiency at delivery, identified associated factors, and assessed immediate neonatal outcomes.
Hussein Mire Hamdi +15 more
wiley +1 more source
Gummies as a Novel Approach to Valorize Rainbow Trout Wastes
ABSTRACT In this study, a potential waste management strategy was developed for the evaluation of marine and freshwater fish waste, which is chemically very similar. To this end, an unmet need has been addressed by converting by‐products from rainbow trout, a cold‐water fish, into functional and nutritious ingredients.
Gonca Alak +8 more
wiley +1 more source
Intractable Rickets as Presenting Feature of Wilson's Disease
Rickets by definition is a condition in which the bone mineralization is defective. Among the large cause of Rickets (Vitamin D deficiency, gastrointestinal disorders, acidosis, renal tubular abnormalities...), Wilson's disease is a relatively rare cause.
A Bahrami-Ahmadi +3 more
doaj
Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: A case report [PDF]
Background: Sixty mutations of claudin 16 coding gene have been reported in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) patients. Recent investigations revealed that a highly conserved glycine-leucine-tryptophan (115G-L-W117)
Bottillo, I +5 more
core +1 more source
MECP2 insufficiency leads to upregulation of miR‐126‐3p, which in turn enhances the endogenous Wnt antagonist DKK1. DKK1 inhibits the canonical Wnt signaling pathway, thereby impairing RUNX2‐dependent osteoblast differentiation. ABSTRACT Rett syndrome (RTT) is a rare neurodevelopmental disorder caused by loss‐of‐function mutations in the gene encoding ...
Shuangshan Dong +12 more
wiley +1 more source
Key Clinical Message Rickets is not a disease of the past. We described a toddler who developed hypophosphatemic rickets associated with the use of elemental formula.
Kamal Abulebda +2 more
doaj +1 more source
Background Osteopenia and rickets are common among extremely low birth weight infants (ELBW,
Parker Bruce R +5 more
doaj +1 more source

