Cargando…

HNF1A gene polymorphisms and cardiovascular risk factors in individuals with late-onset autosomal dominant diabetes: a cross-sectional study

BACKGROUND: Type 2 diabetes mellitus (T2DM) is a genetically heterogeneous disease, hepatocyte nuclear factor-1 homeobox A (HNF1A) single-nucleotide polymorphisms (SNPs) playing a minor role in its pathogenesis. HNF1A is a frequent cause of monogenic diabetes, albeit with early-onset. Some uncommon...

Descripción completa

Detalles Bibliográficos
Autores principales:	Giuffrida, Fernando MA, Furuzawa, Gilberto K, Kasamatsu, Teresa S, Oliveira, Marcos M, Reis, Andre F, Dib, Sergio A
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2009
Materias:	Original Investigation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696421/ https://www.ncbi.nlm.nih.gov/pubmed/19490620 http://dx.doi.org/10.1186/1475-2840-8-28

Ejemplares similares

Ante‐ and postmortem tau in autosomal dominant and late‐onset Alzheimer’s disease
por: Chen, Charles D., et al.
Publicado: (2020)

Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A
por: Marchesin, Valentina, et al.
Publicado: (2019)

Metabolomic and lipidomic signatures in autosomal dominant and late-onset Alzheimer’s disease brains
por: Novotny, Brenna C., et al.
Publicado: (2023)

Autosomal Dominant Tubulointerstitial Kidney Disease HNF1B With Maturity-Onset Diabetes of the Young: A Case Report With Kidney Biopsy
por: Oba, Yuki, et al.
Publicado: (2020)

Familial urothelial cell carcinoma of the bladder with autosomal dominant inheritance and late onset phenotype
por: Brown, Robin, et al.
Publicado: (2014)

Comparing cortical signatures of atrophy between late-onset and autosomal dominant Alzheimer disease
por: Dincer, Aylin, et al.
Publicado: (2020)

The Varied Clinical Presentation of Autosomal Dominant Tubulointerstitial Kidney Disease Due to HNF1β Mutations
por: Bleyer, Anthony J., et al.
Publicado: (2020)

Trajectory of Unawareness of Memory Decline in Individuals With Autosomal Dominant Alzheimer Disease
por: Vannini, Patrizia, et al.
Publicado: (2020)

A Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
por: Lv, Huibin, et al.
Publicado: (2014)

FMRI Complexity Correlates with Tau-PET and Cognitive Decline in Late-Onset and Autosomal Dominant Alzheimer’s Disease
por: Jann, Kay, et al.
Publicado: (2023)

Association of circulating levels of nicotinamide phosphoribosyltransferase (NAMPT/Visfatin) and of a frequent polymorphism in the promoter of the NAMPT gene with coronary artery disease in diabetic and non-diabetic subjects
por: Saddi-Rosa, Pedro, et al.
Publicado: (2013)

Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss
por: Nishio, Shin-ya, et al.
Publicado: (2021)

The role of noise and positive feedback in the onset of autosomal dominant diseases
por: Bosl, William J, et al.
Publicado: (2010)

Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report
por: Varga, Lukas, et al.
Publicado: (2019)

Granuloma annulare and necrobiosis lipoidica in a patient with HNF1A-MODY
por: Brandes, Gabriela Irene Garcia, et al.
Publicado: (2022)

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
por: Olivé, Montse, et al.
Publicado: (2019)

Autosomal dominant and autosomal recessive polycystic kidney disease: hypertension and secondary cardiovascular effect in children
por: Lucchetti, L., et al.
Publicado: (2023)

Involvement of cochlin binding to sulfated heparan sulfate/heparin in the pathophysiology of autosomal dominant late-onset hearing loss (DFNA9)
por: Honda, Tomoko, et al.
Publicado: (2022)

Network Analysis of a Pkd1-Mouse Model of Autosomal Dominant Polycystic Kidney Disease Identifies HNF4α as a Disease Modifier
por: Menezes, Luis F., et al.
Publicado: (2012)

Duplication and deletion upstream of LMNB1 in autosomal dominant adult-onset leukodystrophy
por: Mezaki, Naomi, et al.
Publicado: (2018)

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report
por: Tao, Tian, et al.
Publicado: (2020)

Hyperaldosteronism and cardiovascular risk in patients with autosomal dominant polycystic kidney disease
por: Lai, Silvia, et al.
Publicado: (2016)

Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume
por: Balbo, B.E.P., et al.
Publicado: (2014)

Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3
por: Xiao, Xueshan, et al.
Publicado: (2019)

Characteristics and Distribution of Intracranial Aneurysms in Patients with Autosomal Dominant Polycystic Kidney Disease Compared with the General Population: A Meta-Analysis
por: Haemmerli, Julien, et al.
Publicado: (2023)

Autosomal dominant intellectual disability
por: Wieczorek, Dagmar
Publicado: (2018)

Autosomal dominant polycystic kidney
por: Gudadhe, Rugaved Raghavendra, et al.
Publicado: (2022)

Association of the ACE gene polymorphism with the progression of autosomal dominant polycystic kidney disease.
por: Lee, K. B., et al.
Publicado: (2000)

White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer’s disease
por: Araque Caballero, Miguel Ángel, et al.
Publicado: (2018)

LMNB1 Duplication-Mediated Autosomal Dominant Adult-Onset Leukodystrophy in an Indian Family
por: Bijarnia-Mahay, Sunita, et al.
Publicado: (2021)

Multiple Cardiovascular Manifestations in a Patient with Autosomal Dominant Polycystic Kidney Disease
por: Kang, Young Ran, et al.
Publicado: (2014)

An HNF1α truncation associated with maturity-onset diabetes of the young impairs pancreatic progenitor differentiation by antagonizing HNF1β function
por: Cujba, Ana-Maria, et al.
Publicado: (2022)

Strategies for Outcrossing and Genetic Manipulation of Drosophila Compound Autosome Stocks
por: Martins, Torcato, et al.
Publicado: (2013)

Assessment of fetal modified myocardial performance index in early‐onset and late‐onset fetal growth restriction
por: Zhang, Lina, et al.
Publicado: (2019)

Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy
por: Cirak, Sebahattin, et al.
Publicado: (2010)

Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis
por: Hussain, Hafiz Muhammad Jafar, et al.
Publicado: (2022)

Zebrafish Models of Autosomal Dominant Ataxias
por: Quelle-Regaldie, Ana, et al.
Publicado: (2021)

The infinitesimal model with dominance
por: Barton, Nicholas H, et al.
Publicado: (2023)

Sex Differences in Cognitive Abilities Among Children With the Autosomal Dominant Alzheimer Disease Presenilin 1 E280A Variant From a Colombian Cohort
por: Fox-Fuller, Joshua T., et al.
Publicado: (2021)

Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
por: Duenk, Pascal, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_cccv80aab6neesi4n99lan2qoa