A polymorphic dinucleotide repeat in the 5' flanking region of the human interleukin 11 (IL11) gene

Neuropilin-1 is upregulated in the adaptive response of prostate tumors to androgen-targeted therapies and is prognostic of metastatic progression and patient mortality.

Oncogene·2017

Bimodal in vivo imaging provides early assessment of stem-cell-based photoreceptor engraftment.

Eye (London, England)·2015

Rip3 knockdown rescues photoreceptor cell death in blind pde6c zebrafish.

Cell death and differentiation·2014

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

Clinical genetics·2013

Retina restored and brain abnormalities ameliorated by single-copy knock-in of human NR2E1 in null mice.

Molecular and cellular biology·2012

Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa.

Experimental eye research·2008

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Immunogenetics·2026

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Immunogenetics·2026

Genetic association of immunosenescence to immune decline.

Immunogenetics·2026

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Immunogenetics·2026

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Immunogenetics·2026

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Immunogenetics·2026

Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.

Japanese journal of ophthalmology·2026

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

Prenatal diagnosis·2026

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

Experimental biology and medicine (Maywood, N.J.)·2026

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

medRxiv : the preprint server for health sciences·2026

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

Related Experiment Videos

A polymorphic dinucleotide repeat in the 5' flanking region of the human interleukin 11 (IL11) gene

Related Concept Videos

Neuropilin-1 is upregulated in the adaptive response of prostate tumors to androgen-targeted therapies and is prognostic of metastatic progression and patient mortality.

Bimodal in vivo imaging provides early assessment of stem-cell-based photoreceptor engraftment.

Rip3 knockdown rescues photoreceptor cell death in blind pde6c zebrafish.

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

Retina restored and brain abnormalities ameliorated by single-copy knock-in of human NR2E1 in null mice.

Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa.

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Genetic association of immunosenescence to immune decline.

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

Related Experiment Videos

A polymorphic dinucleotide repeat in the 5' flanking region of the human interleukin 11 (IL11) gene

Related Concept Videos

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