Angiotensin-converting enzyme gene polymorphism in Behçet's disease in Iranian population

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Case reports in ophthalmological medicine·2026

A de novo NR2F1 c.330 C > A variant in Bosch-Boonstra-Schaaf optic atrophy syndrome presenting with early-onset developmental and epileptic encephalopathy.

Molecular biology reports·2026

Novel Variants in PLPBP, SCN1A, and SLC6A1: Genetics, Bioinformatics, and clinical Elucidation of Three Distinct Cases of Developmental and Epileptic Encephalopathy.

Journal of neurogenetics·2026

The promising role of muse cells in regenerative medicine: Mechanisms, applications, and future directions.

Life sciences·2025

Identification of a Novel TRIT1 Mutation in a Consanguineous Iranian-Azeri-Turkish Family With Global Developmental Delay.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience·2025

Genetic insights into progressive myoclonic epilepsies: A case study of KCTD7 mutation in an Iranian-Azeri-Turkish family.

Epilepsy & behavior reports·2025

A novel ZEB1 splice-site variant causing early-onset type 3 posterior polymorphous corneal dystrophy and suspected corneal ectasia.

Ophthalmic genetics·2026

Intrafamilial phenotypic variability in CRX-associated retinopathy due to a frameshift variant (c.661del).

Ophthalmic genetics·2026

PCARE-associated inherited retinal diseases: clinical and molecular insights from a Portuguese population.

Ophthalmic genetics·2026

First CDH3-related HJMD case in a black patient: novel variants and diagnostic odyssey.

Ophthalmic genetics·2026

Crossover to acetazolamide for the treatment of cystoid fluid collections in X-linked retinoschisis: the REAXIS study.

Ophthalmic genetics·2026

Unique retinal phenotype may support pathogenicity of FSCN2 in inherited retinal degenerations: a case report and review of the literature.

Ophthalmic genetics·2026

Correction: Shared and condition-associated gut microbiota alterations in older adults with depression and constipation: evidence from the American Gut Project.

Frontiers in microbiology·2026

Clinically altered brain activity may not look like aged brain activity: Implications for brain-age modeling and biomarker strategies.

Alzheimer's & dementia (New York, N. Y.)·2026

Research progress and application prospects of multi-omics integration strategies in precision risk stratification of type 1 diabetes mellitus.

Frontiers in immunology·2026

Investigating the causal impact of gut microbiota on periodontitis based on Mendelian randomization, bulk transcriptomics, and single-cell transcriptomics.

Frontiers in cell and developmental biology·2026

Partitioned blood pressure polygenic risk reveals differential genetic effects of tissue-specific enhancers and their interactions on cardiovascular disease.

Research square·2026

Enhanced chromatin compaction is associated with de novo expression of a nuclear microprotein, global loss of H3 acetylation and local transcriptional changes in retinal rod photoreceptors.

Research square·2026

Related Experiment Videos

Angiotensin-converting enzyme gene polymorphism in Behçet's disease in Iranian population

Related Concept Videos

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

A de novo NR2F1 c.330 C > A variant in Bosch-Boonstra-Schaaf optic atrophy syndrome presenting with early-onset developmental and epileptic encephalopathy.

Novel Variants in PLPBP, SCN1A, and SLC6A1: Genetics, Bioinformatics, and clinical Elucidation of Three Distinct Cases of Developmental and Epileptic Encephalopathy.

The promising role of muse cells in regenerative medicine: Mechanisms, applications, and future directions.

Identification of a Novel TRIT1 Mutation in a Consanguineous Iranian-Azeri-Turkish Family With Global Developmental Delay.

Genetic insights into progressive myoclonic epilepsies: A case study of KCTD7 mutation in an Iranian-Azeri-Turkish family.

A novel ZEB1 splice-site variant causing early-onset type 3 posterior polymorphous corneal dystrophy and suspected corneal ectasia.

Intrafamilial phenotypic variability in CRX-associated retinopathy due to a frameshift variant (c.661del).

PCARE-associated inherited retinal diseases: clinical and molecular insights from a Portuguese population.

First CDH3-related HJMD case in a black patient: novel variants and diagnostic odyssey.

Crossover to acetazolamide for the treatment of cystoid fluid collections in X-linked retinoschisis: the REAXIS study.

Unique retinal phenotype may support pathogenicity of FSCN2 in inherited retinal degenerations: a case report and review of the literature.

Correction: Shared and condition-associated gut microbiota alterations in older adults with depression and constipation: evidence from the American Gut Project.

Clinically altered brain activity may not look like aged brain activity: Implications for brain-age modeling and biomarker strategies.

Research progress and application prospects of multi-omics integration strategies in precision risk stratification of type 1 diabetes mellitus.

Investigating the causal impact of gut microbiota on periodontitis based on Mendelian randomization, bulk transcriptomics, and single-cell transcriptomics.

Partitioned blood pressure polygenic risk reveals differential genetic effects of tissue-specific enhancers and their interactions on cardiovascular disease.

Enhanced chromatin compaction is associated with de novo expression of a nuclear microprotein, global loss of H3 acetylation and local transcriptional changes in retinal rod photoreceptors.

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Angiotensin-converting enzyme gene polymorphism in Behçet's disease in Iranian population

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