Results 31 to 40 of about 2,410 (172)
Congenital glucose‐galactose malabsorption: A case report with a novel SLC5A1 mutation [PDF]
Key Clinical MessageA three‐day‐old newborn girl presented with decreased feeding and dehydration. She was sick and in shock. She had renal impairment and hypernatremia. With the resumption of breast feeding, she developed watery stools and hypernatremia. Glucose‐Galactose Malabsorption was suspected and confirmed by the presence of a likely pathogenic
Manar Al‐lawama +3 more
openaire +2 more sources
A risk model of gene signatures for predicting platinum response and survival in ovarian cancer
Background Ovarian cancer (OC) is the deadliest tumor in the female reproductive tract. And increased resistance to platinum-based chemotherapy represents the major obstacle in the treatment of OC currently. Robust and accurate gene expression models are
Siyu Chen +5 more
doaj +1 more source
Researchers have long awaited the technology to develop an in vitro kidney model. Here, we establish a rapid fabricating technique for kidney-like tissues (cysts) using a combination of an organ-derived extracellular matrix (ECM) gel format culture ...
Yusuke Sakai +5 more
doaj +1 more source
Even though metformin is widely used to treat type2 diabetes, reducing glycaemia and body weight, the mechanisms of action are still elusive. Recent studies have identified the gastrointestinal tract as an important site of action.
Ming Yang +14 more
doaj +1 more source
Stx2 Induces Differential Gene Expression and Disturbs Circadian Rhythm Genes in the Proximal Tubule
Shiga toxin-producing Escherichia coli (STEC) causes proximal tubular defects in the kidney. However, factors altered by Shiga toxin (Stx) within the proximal tubules are yet to be shown.
Fumiko Obata +4 more
doaj +1 more source
Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review
Glucose-galactose malabsorption is a rare inherited autosomal recessive genetic defect. A mutation in the glucose sodium-dependent transporter-1 gene will alter the transportation and absorption of glucose and galactose in the intestine.
Nawaf W. Alruwaili, Fahad Alshdayed
doaj +1 more source
Local environment‐driven adaptive evolution in a marine invasive ascidian (Molgula manhattensis)
Elucidating molecular mechanisms of environment‐driven adaptive evolution in marine invaders is crucial for understanding invasion success and further predicting their future invasions.
Yiyong Chen +4 more
doaj +1 more source
Changes in the gut microbiome during fasting‐induced molting and its effects on gut–liver function [PDF]
During fasting, harmful microbiota and metabolites rise, triggering intestinal injury and activation of the TGF‐β signaling pathway, which enhances intestinal stem cell proliferation. Concurrently, hepatic function declines, indicated by increased hepatic and serum bile acids and upregulation of the non‐classical bile acid synthesis pathway.
Zhang H +11 more
europepmc +2 more sources
Vitamins and microelements play essential roles in mammalian ovarian physiology, including follicle development, ovulation, and synthesis and secretion of hormones and growth factors.
Yajun Guo +6 more
doaj +1 more source
Philipp Kreisz was not included as an author in the original publication [...]
Philippa K. Brosch +12 more
openaire +1 more source

