A common genetic origin of specific dyslexia and insulin-dependent diabetes mellitus?

Genetic markers for glutamic acid decarboxylase do not predict insulin-dependent diabetes mellitus in pairs of affected siblings.

Human genetics·2016

Precision measurement of the neutron twist-3 matrix element d(2)(n): probing color forces.

Physical review letters·2014

A transparent Pyrex μ-reactor for combined in situ optical characterization and photocatalytic reactivity measurements.

The Review of scientific instruments·2013

The effects of multidisciplinary rehabilitation: RePCa-a randomised study among primary prostate cancer patients.

British journal of cancer·2013

Measurements of parity-violating asymmetries in electron-deuteron scattering in the nucleon resonance region.

Physical review letters·2013

Random modelling of contagious diseases.

Acta biotheoretica·2013

Diagnostic and mechanistic roles of miR-5584-5p in endometriosis via the FZD2-mediated Wnt/β-catenin EMT axis.

Hereditas·2026

Multi-omics mapping of TIMP1-associated stromal-myeloid remodeling in autoimmune gastritis and gastric cancer.

Hereditas·2026

Beyond the variant: hereditary cancer awareness in the multi-omics era.

Hereditas·2026

Hereditary breast cancer: emerging roles of non-coding RNAs.

Hereditas·2026

The prognostic value of miR-363-5p in colorectal cancer and its associated molecular mechanisms.

Hereditas·2026

MicroRNA-345-3p expression inhibits colorectal cancer liver metastasis by targeting KHDRBS1 and TGF-β signaling pathway.

Hereditas·2026

Genomic ascertainment of systemic autoinflammatory diseases: a retrospective cohort study in two population-based biobanks.

The Lancet. Rheumatology·2026

Epidemiological and molecular insights into human lice (Anoplura: Pediculidae) in France: genetic diversity and DNA barcoding.

Parasite (Paris, France)·2026

Prevalence and potential risk factors associated with idiopathic epilepsy in Golden Retrievers.

Journal of veterinary internal medicine·2026

Comprehensive assessment of the genotype-phenotype spectrum and treatment for monoallelic insulin receptoropathy in a cohort of 505 people.

Research square·2026

Neurobiological etiology of impulsivity in the context of aggressive behaviors in schizophrenia.

Psychiatria polska·2026

A Study on the Differences in the Probability of Iron Deficiency Anemia and the Severity of Anemia among People with Different Blood Types.

Clinical laboratory·2026

Related Experiment Videos

A common genetic origin of specific dyslexia and insulin-dependent diabetes mellitus?

Related Concept Videos

Genetic markers for glutamic acid decarboxylase do not predict insulin-dependent diabetes mellitus in pairs of affected siblings.

Precision measurement of the neutron twist-3 matrix element d(2)(n): probing color forces.

A transparent Pyrex μ-reactor for combined in situ optical characterization and photocatalytic reactivity measurements.

The effects of multidisciplinary rehabilitation: RePCa-a randomised study among primary prostate cancer patients.

Measurements of parity-violating asymmetries in electron-deuteron scattering in the nucleon resonance region.

Random modelling of contagious diseases.

Diagnostic and mechanistic roles of miR-5584-5p in endometriosis via the FZD2-mediated Wnt/β-catenin EMT axis.

Multi-omics mapping of TIMP1-associated stromal-myeloid remodeling in autoimmune gastritis and gastric cancer.

Beyond the variant: hereditary cancer awareness in the multi-omics era.

Hereditary breast cancer: emerging roles of non-coding RNAs.

The prognostic value of miR-363-5p in colorectal cancer and its associated molecular mechanisms.

MicroRNA-345-3p expression inhibits colorectal cancer liver metastasis by targeting KHDRBS1 and TGF-β signaling pathway.

Genomic ascertainment of systemic autoinflammatory diseases: a retrospective cohort study in two population-based biobanks.

Epidemiological and molecular insights into human lice (Anoplura: Pediculidae) in France: genetic diversity and DNA barcoding.

Prevalence and potential risk factors associated with idiopathic epilepsy in Golden Retrievers.

Comprehensive assessment of the genotype-phenotype spectrum and treatment for monoallelic insulin receptoropathy in a cohort of 505 people.

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A common genetic origin of specific dyslexia and insulin-dependent diabetes mellitus?

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