Related Experiment Videos
Molecular characterisation of beta thalassaemia heterozygotes in Brazil
Journal of Medical Genetics
|September 1, 1993
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
PI3K inhibition by BKM120 results in anti-proliferative effects on corticotroph tumor cells.
Journal of endocrinological investigation·2022
Perinatal exposure to a high-fat diet alters proopiomelanocortin, neuropeptide Y and dopaminergic receptors gene expression and the food preference in offspring adult rats.
Brazilian journal of biology = Revista brasleira de biologia·2021
Clostridium difficile toxins or infection induce upregulation of adenosine receptors and IL-6 with early pro-inflammatory and late anti-inflammatory pattern.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas·2020
Beneficial Effects of Soluble Guanylyl Cyclase Stimulation and Activation in Sickle Cell Disease Are Amplified by Hydroxyurea: In Vitro and In Vivo Studies.
The Journal of pharmacology and experimental therapeutics·2020
A Brazilian regional basic diet-induced chronic malnutrition drives liver inflammation with higher ApoA-I activity in C57BL6J mice.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas·2020
Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.
Journal of medical genetics·2026
Solid tumours in RASopathies: insights from a large monocentric cohort and systematic review of the literature.
Journal of medical genetics·2026
Hypertrophic cardiomyopathy: a genome-wide association meta-analysis and polygenic risk score.
Journal of medical genetics·2026
Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.
Journal of medical genetics·2026
Exploring the clinical and mutational spectrum of MORC2-associated disorders.
Journal of medical genetics·2026
Founder variant in OTOG causing non-syndromic sensorineural hearing loss in Irish traveller population.
Journal of medical genetics·2026
Homozygous variants in ZSWIM6 cause severe syndromic short stature and developmental delay.
Hormone research in paediatrics·2026
Before hormones: early sex-specific mechanisms shaping nervous system development, function, and postnatal disease susceptibility.
Frontiers in behavioral neuroscience·2026
The genome sequence of the Silver Colonel, Odontomyia argentata (Fabricius, 1794) (Diptera: Stratiomyidae).
Wellcome open research·2026
The genome sequence of a nematode, Thelazia callipaeda Railliet & Henry, 1910 (Rhabditida: Thelaziidae).
Wellcome open research·2026
Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency.
The Journal of molecular diagnostics : JMD·2026