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Modulation of Insulin Sensitivity by Insulin-Degrading Enzyme [PDF]

open access: yesBiomedicines, 2021
Insulin-degrading enzyme (IDE) is a highly conserved and ubiquitously expressed metalloprotease that degrades insulin and several other intermediate-size peptides.
Carlos M. González-Casimiro   +8 more
doaj   +6 more sources

Assessment of insulin sensitivity/resistance

open access: yesIndian Journal of Endocrinology and Metabolism, 2015
Insulin resistance is one pretty troublesome entity which very commonly aggravates metabolic syndrome. Many methods and indices are available for the estimation of insulin resistance. It is essential to test and validate their reliability before they can
Manish Gutch   +4 more
doaj   +3 more sources

Molecular and Cellular Bases of Lipodystrophy Syndromes

open access: yesFrontiers in Endocrinology, 2022
Lipodystrophy syndromes are rare diseases originating from a generalized or partial loss of adipose tissue. Adipose tissue dysfunction results from heterogeneous genetic or acquired causes, but leads to similar metabolic complications with insulin ...
Jamila Zammouri   +20 more
doaj   +1 more source

Pregnancy in Women With Monogenic Diabetes due to Pathogenic Variants of the Glucokinase Gene: Lessons and Challenges

open access: yesFrontiers in Endocrinology, 2022
Heterozygous loss-of-function variants of the glucokinase (GCK) gene are responsible for a subtype of maturity-onset diabetes of the young (MODY). GCK-MODY is characterized by a mild hyperglycemia, mainly due to a higher blood glucose threshold for ...
José Timsit   +14 more
doaj   +1 more source

Insulin resistance and insulin sensitizing agents [PDF]

open access: yesMetabolism, 2021
Insulin resistance is a common feature of obesity and type 2 diabetes, but novel approaches of diabetes subtyping (clustering) revealed variable degrees of insulin resistance in people with diabetes. Specifically, the severe insulin resistant diabetes (SIRD) subtype not only exhibits metabolic abnormalities, but also bears a higher risk for ...
Lucia, Mastrototaro, Michael, Roden
openaire   +2 more sources

Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)

open access: yesOrphanet Journal of Rare Diseases, 2022
Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA gene. The objective of the French National Diagnosis and Care Protocol (PNDS; Protocole National
H. Mosbah   +36 more
doaj   +1 more source

Enhanced cell viscosity: A new phenotype associated with lamin A/C alterations

open access: yesiScience, 2023
Summary: Lamin A/C is a well-established key contributor to nuclear stiffness and its role in nucleus mechanical properties has been extensively studied.
Cécile Jebane   +12 more
doaj   +1 more source

Serum dihydroceramides correlate with insulin sensitivity in humans and decrease insulin sensitivity in vitro

open access: yesJournal of Lipid Research, 2022
Serum ceramides, especially C16:0 and C18:0 species, are linked to CVD risk and insulin resistance, but details of this association are not well understood.
Simona Zarini   +10 more
doaj   +1 more source

Estimation of reference intervals of insulin resistance (HOMA), insulin sensitivity (Matsuda), and insulin secretion sensitivity indices (ISSI-2) in Polish young people

open access: yesAnnals of Agricultural and Environmental Medicine, 2020
Introduction Insulin resistance is becoming an increasingly widespread problem worldwide. For its determination indirect indices of insulin resistance or insulin sensitivity have used. Those indices based on simultaneous measurements of blood glucose and
Sylwia Płaczkowska   +3 more
doaj   +1 more source

European lipodystrophy registry: background and structure

open access: yesOrphanet Journal of Rare Diseases, 2020
Background Lipodystrophy syndromes comprise a group of extremely rare and heterogeneous diseases characterized by a selective loss of adipose tissue in the absence of nutritional deprivation or catabolic state. Because of the rarity of each lipodystrophy
Julia von Schnurbein   +24 more
doaj   +1 more source

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