Nuclear Receptor Variants in Liver Disease [PDF]
This review aims to provide a snapshot of the actual state of knowledge on genetic variants of nuclear receptors (NR) involved in regulating important aspects of liver metabolism.
Lammert, Frank+2 more
core +2 more sources
Diabetes mellitus and ischemic heart disease. the role of ion channels [PDF]
Diabetes mellitus is one the strongest risk factors for cardiovascular disease and, in particular, for ischemic heart disease (IHD). The pathophysiology of myocardial ischemia in diabetic patients is complex and not fully understood: some diabetic ...
De Marchis, Marialaura+8 more
core +2 more sources
Patient Attitudes Toward Genetic Testing for Inherited Predispositions to Hematologic Malignancies [PDF]
Although inherited predispositions to hematologic malignancies have previously been considered extremely rare, approximately 12 causative genes have been implicated in the last decade.
Beecroft, Taylor
core +1 more source
Background and Objectives: The aim of the following cross-sectional study is to determine the association between human leukocyte antigen (HLA) alleles and outcomes in patients presenting to the emergency department (ED) with SARS-CoV-2 infection ...
Ester Lobato-Martinez+8 more
doaj +1 more source
Genetically selected baby free of inherited predisposition to early-onset Alzheimer's disease [PDF]
Merle Spriggs
openalex +1 more source
Untangling Cultural Differences in Behavioral, Physiological, and Psychological Symptoms of Dementia and Alzheimer’s Disease [PDF]
According to the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR; 4th ed. Revised; American Psychiatric Association) and (BPSD) there are many behavioral, physiological, and psychological issues that have been correlated with the ...
Avant, John S
core +1 more source
CLINICAL APPLICABILITY OF PROPOSED ALGORITHM FOR IDENTIFYING INDIVIDUALS AT RISK FOR HEREDITARY HEMATOLOGIC MALIGNANCIES [PDF]
Over the past decade, more than 12 genes have been identified to cause hereditary predispositions to hematologic malignancies. These syndromes are characterized by an increased risk to develop myelodysplastic syndrome (MDS), acute myeloid leukemia (AML),
Clifford, Maggie
core +1 more source
Resumen: Objetivo: Determinar la existencia de un patrón familiar de agregación del síndrome de intestino irritable (SII). Diseño: Es un estudio de casos y controles con proporción 1:2, llevado a cabo en una consulta externa de medicina general-familiar.
José M. Ramírez Aranda+4 more
doaj
DISSECTING THE GENETIC SUSCEPTIBILITY TO GRAVES’ DISEASE IN A COHORT OF PATIENTS OF ITALIAN ORIGIN
Graves’ disease (GD) is an autoimmune oligogenic disorder with a strong hereditary component. Several GD-susceptibility genes have been identified and confirmed during the last two decades.
Angela eLombardi+9 more
doaj +1 more source
Association between SNCA Intron and genetic predisposition to sporadic Parkinson's disease: a meta-analysis based on 49576 individuals [PDF]
Peng Li+4 more
openalex +1 more source