Sister-chromatid exchange in 4 human races

Obestatin and adropin in Prader-Willi syndrome and nonsyndromic obesity: Associations with weight, BMI-z, and HOMA-IR.

Pediatric obesity·2018

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.

Clinical genetics·2017

Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.

Journal of intellectual disability research : JIDR·2017

Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi Syndrome.

Journal of clinical epigenetics·2017

EVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME.

The Journal of rare disorders·2016

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

Journal of endocrinological investigation·2015

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mutation research·2026

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Mutation research·2026

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Mutation research·2026

Non-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression.

Mutation research·2026

miR-145-5p induces ferroptosis by targeting Notch2 to suppress melanoma progression.

Mutation research·2026

Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications.

Mutation research·2026

HIPK4 is a novel gene associated with teratozoospermia and male infertility.

Human reproduction open·2026

Edge Preserved U-Net for chromosome edge detection.

Computational biology and chemistry·2026

A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

International journal of molecular sciences·2026

Circadian Disruption Is Associated with Elevated Whole-Semen mtDNA Copy Number and Implicates CRY1 as a Candidate Regulator in Humans and Mice.

International journal of molecular sciences·2026

A single-cell multi-omic atlas of the human pancreas reveals potential for cellular plasticity across development, health, and disease.

Cell metabolism·2026

Ataxin-2 regulates the synaptonemal complex to ensure chromosome pairing during female meiosis.

Genetics·2026

Related Experiment Videos

Sister-chromatid exchange in 4 human races

Related Concept Videos

Obestatin and adropin in Prader-Willi syndrome and nonsyndromic obesity: Associations with weight, BMI-z, and HOMA-IR.

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.

Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.

Examination of Global Methylation and Targeted Imprinted Genes in Prader-Willi Syndrome.

EVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME.

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.

The role of KIT mutations in oral melanoma and disease progression: A literature review on early detection and targeted therapy.

Mothers against decapentaplegic homolog 3-activated FAT atypical cadherin 2 regulates programmed death ligand-1 to mediate immune evasion in lung squamous cell carcinoma.

Potential targets and molecular mechanisms of curcumin in treating Laryngeal and Pharyngeal Carcinoma throat cancer based on network pharmacology and bioinformatics analysis.

Non-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression.

miR-145-5p induces ferroptosis by targeting Notch2 to suppress melanoma progression.

Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications.

HIPK4 is a novel gene associated with teratozoospermia and male infertility.

Edge Preserved U-Net for chromosome edge detection.

A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

Circadian Disruption Is Associated with Elevated Whole-Semen mtDNA Copy Number and Implicates CRY1 as a Candidate Regulator in Humans and Mice.

A single-cell multi-omic atlas of the human pancreas reveals potential for cellular plasticity across development, health, and disease.

Ataxin-2 regulates the synaptonemal complex to ensure chromosome pairing during female meiosis.

Related Experiment Videos

Sister-chromatid exchange in 4 human races

Related Concept Videos

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