Results 101 to 110 of about 54,466 (294)
The dermatological spectrum of Turner syndrome
, 1994 Turner syndrome, characterized by monosomy of X chromosome, has a peculiar phenotype, including short stature, sexual infantilism, cardiovascular, renal, skeletal and skin abnormalities (in particular melanocytic naevi and skin appendage abnormalities ...
Brazzelli V. +8 more
core +1 more source
Sex‐Specific Regulation of Glycemic Homeostasis by Theabrownin from Pu‐erh Tea
Advanced Science, EarlyView.Pu‐erh tea's key component, theabrownin (TB), lowers blood glucose in a sex‐specific manner. In females, estrogen boosts intestinal MUC2 production, which dramatically enhances TB's ability to inhibit the carbohydrate‐digesting enzyme α‐glucosidase.
Yang Li +22 more
wiley +1 more source
Stem Cell Research, 2017 A major cause of spontaneous abortions is chromosomal abnormality of foetal cells. We report the generation of an induced pluripotent stem cell line from the fibroblasts isolated from chorionic villi of an early spontaneously aborted foetus with Turner ...
Shagufta Parveen +2 more
doaj +1 more source
Oral manifestations of patients with Turner syndrome
, 2000 Objective: The purpose of this study was to conduct a complete analysis of orofacial abnormalities of patients with Turner syndrome. Study Design: Twenty nine patients with Turner syndrome and 30 without Turner syndrome (control group) were studied.
Szilágyi, Andrea +3 more
core +1 more source
G3BP1 Succinylation at K413 is Critical for Cardiac Function by Modulating PI3K‐AKT‐mTOR Signal Axis
Advanced Science, EarlyView.Schematic illustrating the impact of G3BP1 succinylation at K413 on cardiac function. In the healthy human heart, G3BP1 succinylation maintains homeostatic mTOR signaling. In patients with dilated cardiomyopathy (DCM) and heart failure (HF), G3BP1 de‐succinylation induces RagA expression and disrupts the binding of the TSC1/2 complex, leading to the ...
Yuan Zhang +9 more
wiley +1 more source
Parsonage-Turner syndrome revealing Lyme borreliosis.
, 2009 International audienceParsonage-Turner syndrome, also known as acute brachial neuritis or neuralgic amyotrophy, can be caused by various infectious agents. We report on four patients who experienced Parsonage-Turner syndrome as the first manifestation of
Michel, Fabrice +6 more
core +1 more source
Advanced Science, EarlyView.THUMPD1 drives a tumor‐suppressive signaling cascade in lung adenocarcinoma by promoting IGF2R expression. IGF2R associates with PPP2R1A to suppress AKT and activate AMPK, leading to SLC31A1 upregulation and copper accumulation. Elevated copper disrupts mitochondrial metabolism and induces excessive mitophagy, thereby restraining tumor growth and ...
Kai Wu +10 more
wiley +1 more source
Turner syndrome and osteoporosis
, 2019 Turner syndrome is one of the most common sex chromosomal anomalies, characterized by the complete or partial loss of one X chromosome. Females with Turner syndrome are characterized by skeletal abnormalities, short stature and primary ovarian ...
Lambrinoudaki, I. +2 more
core
Síndrome de Turner: aspectos clínicos e avaliação do tratamento da baixa estatura com hormônio de crescimento em um Serviço de Referência em Endocrinologia Pediátrica [PDF]
, 2011 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Brinhosa, Maria Eduarda Dias
core
Parent-of-origin effects in Turner Syndrome patients
, 2015 Turner Syndrome patients have a single X chromosome, without a partner, X or Y. It has been suggested that the inheritance of the maternal X or paternal X may affect the severity of Turner Syndrome, as well as the incidence of mental disorders in Turner ...
Jada Wang (760247) +2 more
core +1 more source