Mancera-Rincón et al., 2024 - Google Patents
Maturity-onset diabetes of the young type 7 (MODY7) and the krüppellike factor 11 mutation (KLF11). A reviewMancera-Rincón et al., 2024
- Document ID
- 7074409450028950076
- Author
- Mancera-Rincón P
- Luna-España M
- Rincon O
- Guzmán I
- Alvarez M
- Publication year
- Publication venue
- Current Diabetes Reviews
External Links
Snippet
Introduction: Maturity-onset diabetes of the young (MODY) is a rare disease due to a single gene mutation that affects several family members in most cases. The Krüppel-like factor 11 (KLF11) gene mutation is associated with decreased insulin sensitivity to high glucose …
- 108010074864 Factor XI 0 title abstract description 5
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/04—Endocrine or metabolic disorders
- G01N2800/042—Disorders of carbohydrate metabolism, e.g. diabetes, glucose metabolism
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay
- G01N33/564—Immunoassay; Biospecific binding assay for pre-existing immune complex or autoimmune disease, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Urakami | Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment | |
Umpierrez et al. | Narrative review: ketosis-prone type 2 diabetes mellitus | |
Vaxillaire et al. | Genetic basis of maturity-onset diabetes of the young | |
Yorifuji et al. | Comprehensive molecular analysis of Japanese patients with pediatric‐onset MODY‐type diabetes mellitus | |
den Uyl et al. | Metabolic effects of high‐dose prednisolone treatment in early rheumatoid arthritis: Balance between diabetogenic effects and inflammation reduction | |
Nishimura et al. | Slowly progressive type 1 diabetes mellitus: current knowledge and future perspectives | |
Yahaya et al. | Genetics and pathophysiology of maturity-onset diabetes of the young (MODY): A Review of current trends | |
Mohan et al. | Associations of β-cell function and insulin resistance with youth-onset type 2 diabetes and prediabetes among Asian Indians | |
Hegele et al. | Genetic and physiological insights into the metabolic syndrome | |
Schmid et al. | Globular and full-length adiponectin induce NO-dependent vasodilation in resistance arteries of Zucker lean but not Zucker diabetic fatty rats | |
Wojcik et al. | The elevated gene expression level of the A2B adenosine receptor is associated with hyperglycemia in women with gestational diabetes mellitus | |
Oliveira et al. | Maturity-onset diabetes of the young: from a molecular basis perspective toward the clinical phenotype and proper management | |
Yew et al. | tRNA methyltransferase homologue gene TRMT 10A mutation in young adult‐onset diabetes with intellectual disability, microcephaly and epilepsy | |
Miranda‐Lora et al. | Associations of common variants in the SLC16A11, TCF7L2, and ABCA1 genes with pediatric‐onset type 2 diabetes and related glycemic traits in families: a case‐control and case‐parent trio study | |
Moon et al. | Genetic polymorphisms in peroxisome proliferator‐activated receptor γ are associated with Type 2 diabetes mellitus and obesity in the Korean population | |
Yeow et al. | Preserved glucagon-like peptide-1 responses to oral glucose, but reduced incretin effect, insulin secretion and sensitivity in young Asians with type 2 diabetes mellitus | |
Andersen et al. | PGC-1α Gly482Ser polymorphism associates with hypertension among Danish whites | |
Harsunen et al. | Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register | |
Bertoccini et al. | The vitamin D receptor functional variant rs2228570 (C> T) does not associate with type 2 diabetes mellitus | |
Opstad et al. | Reduced leukocyte telomere lengths and sirtuin 1 gene expression in long‐term survivors of type 1 diabetes: A Dialong substudy | |
Mancera-Rincón et al. | Maturity-onset diabetes of the young type 7 (MODY7) and the krüppellike factor 11 mutation (KLF11). A review | |
Yamakage et al. | Association of protein tyrosine phosphatase 1B gene polymorphism with the effects of weight reduction therapy on bodyweight and glycolipid profiles in obese patients | |
Montagnana et al. | The Pro12Ala polymorphism of the PPARG gene is not associated with the metabolic syndrome in an urban population of middle‐aged Swedish individuals | |
Gomathi et al. | The-866G/A polymorphism in the promoter of the UCP2 gene is associated with risk for type 2 diabetes and with decreased insulin levels | |
Langer et al. | The novel GCK variant p. Val455Leu associated with hyperinsulinism is susceptible to allosteric activation and is conducive to weight gain and the development of diabetes |