Ambral syndrome and congenital generalized hypertrichosis

Variants rs2758346, rs5746094, and rs2758331 of SOD2 gene: association study with breast cancer in a Mexican population and their analysis in silico.

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SOD1 gene variants rs4817415, rs2070424, and rs1041740 and their association with breast cancer risk.

European review for medical and pharmacological sciences·2023

Influence of nitric oxide signaling mechanisms in cancer.

International journal of immunopathology and pharmacology·2022

Mutational spectrum of the iduronate-2-sulfatase gene in Mexican patients with Hunter syndrome.

European review for medical and pharmacological sciences·2022

Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population.

European review for medical and pharmacological sciences·2021

The rs1008562, rs2234671, and rs3138060 polymorphisms of the CXCR1 gene are associated with breast cancer risk in a Mexican population.

European review for medical and pharmacological sciences·2020

Genetic Architecture of Pediatric Cardiomyopathies Assessed by Whole-Exome Sequencing: Insights Into Early-Onset and Syndromic Forms.

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Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

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Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum.

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A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

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Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1-Related Noonan Syndrome.

Clinical genetics·2026

Hereditary Polyneuropathy Experience of a Tertiary Single-Center in Türkiye: Beyond the Tip of the Iceberg.

Clinical genetics·2026

Note on a Weighted Geometric Inequality in Hyperbolic Space.

Journal of geometric analysis·2026

An Energy-Efficient Hybrid LoRa-Wi-Fi Architecture for Real- Time Water Quality Monitoring and Machine Learning-Based Trend Forecasting.

Sensors (Basel, Switzerland)·2026

A Prolonged Multimodal Lateral Flow Immunoassay Enabled by Synergistic Peroxidase-Heme Nanohybrids.

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Persistent Unexplained Hydronephrosis in an Adolescent: A Multimodal Imaging Challenge.

Journal of clinical ultrasound : JCU·2026

Point-of-Care Ultrasound-Guided Hydrodissection in Emergency Care: A Structured Narrative Review of Perineural and Related Musculoskeletal Applications.

Cureus·2026

Turbulent seismoacoustic imprints during a hurricane landfall.

Science (New York, N.Y.)·2026

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Ambral syndrome and congenital generalized hypertrichosis

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Variants rs2758346, rs5746094, and rs2758331 of SOD2 gene: association study with breast cancer in a Mexican population and their analysis in silico.

SOD1 gene variants rs4817415, rs2070424, and rs1041740 and their association with breast cancer risk.

Influence of nitric oxide signaling mechanisms in cancer.

Mutational spectrum of the iduronate-2-sulfatase gene in Mexican patients with Hunter syndrome.

Association between rs61764370, rs9266, and rs140080026 polymorphisms of the KRAS gene and breast cancer risk in a Mexican population.

The rs1008562, rs2234671, and rs3138060 polymorphisms of the CXCR1 gene are associated with breast cancer risk in a Mexican population.

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Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.

Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum.

A De Novo DHX16 Variant Associated With Neuromuscular Oculoauditory Syndrome Regulates Pre-mRNA Splicing In Vitro.

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Hereditary Polyneuropathy Experience of a Tertiary Single-Center in Türkiye: Beyond the Tip of the Iceberg.

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Ambral syndrome and congenital generalized hypertrichosis

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