A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogene

At-home vs In-office Bleaching: An Updated Systematic Review and Meta-analysis.

Operative dentistry·2025

ARID1B-related disorder in 87 adults: Natural history and self-sustainability.

Genetics in medicine open·2024

Clinical performance of posterior restorations using a universal adhesive over moist and dry dentin: A 36-month double-blind split-mouth randomized clinical trial.

Journal of dentistry·2024

Demographic structure across all known populations of the rheophyte Dyckia brevifolia Baker (Bromeliaceae) in the Itajaí-Açu River, Southern Brazil.

Brazilian journal of biology = Revista brasleira de biologia·2024

Effect of silver diamine fluoride on the longevity of the bonding properties to caries-affected dentine.

Journal of dentistry·2024

Color Match of a Universal-shade Composite Resin for Restoration of Non-carious Cervical Lesions: An Equivalence Randomized Clinical Trial.

Operative dentistry·2023

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

Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.

Journal of medical genetics·2026

Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.

Journal of medical genetics·2026

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

Journal of medical genetics·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Dynamic effects of short-term storage temperature and duration on the transcriptome and functional pathways of umbilical cord blood-derived NK cells.

Journal of immunological methods·2026

MAD2B guides chromosome stability in mitosis via the MAD2B-CIP2A signaling axis.

Journal of molecular cell biology·2026

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Frontiers in cell and developmental biology·2026

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

Planta·2026

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

The FEBS journal·2026

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Stem cell reports·2026

Related Experiment Videos

A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its

Related Concept Videos

At-home vs In-office Bleaching: An Updated Systematic Review and Meta-analysis.

ARID1B-related disorder in 87 adults: Natural history and self-sustainability.

Clinical performance of posterior restorations using a universal adhesive over moist and dry dentin: A 36-month double-blind split-mouth randomized clinical trial.

Demographic structure across all known populations of the rheophyte Dyckia brevifolia Baker (Bromeliaceae) in the Itajaí-Açu River, Southern Brazil.

Effect of silver diamine fluoride on the longevity of the bonding properties to caries-affected dentine.

Color Match of a Universal-shade Composite Resin for Restoration of Non-carious Cervical Lesions: An Equivalence Randomized Clinical Trial.

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Founder variant in OTOG causing non-syndromic sensorineural hearing loss in Irish traveller population.

Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.

Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Dynamic effects of short-term storage temperature and duration on the transcriptome and functional pathways of umbilical cord blood-derived NK cells.

MAD2B guides chromosome stability in mitosis via the MAD2B-CIP2A signaling axis.

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Related Experiment Videos

A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its...

Related Concept Videos

Related Articles

A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its