A system of nomenclature for band patterns of mouse chromosomes

Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.

Clinical genetics·2008

Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.

Journal of medical genetics·2008

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study.

American journal of human genetics·2007

The human genome project: implications for the endocrinologist.

Journal of pediatric endocrinology & metabolism : JPEM·2002

Spectrum of MECP2 mutations in Rett syndrome.

Brain & development·2001

Multi-exon deletions of the FBN1 gene in Marfan syndrome.

BMC medical genetics·2001

Sustainable integrative cell biology: CENP-C is guilty by association.

Chromosoma·2025

Molecular and bioinformatics analysis of long non-coding RNAs in cervical cancer.

Chromosoma·2025

The synaptonemal complex component corolla regulates meiotic crossover formation in Drosophila melanogaster.

Chromosoma·2025

Phosphorylation as a regulatory mechanism of HP1 protein multifunctionality.

Chromosoma·2025

RAD18 promotes cell malignant behaviors of esophageal squamous cell carcinoma by modulating ATM/STAT3/PD-L1.

Chromosoma·2025

Regulatory effects of lncRNA PVT1 on transcriptome in human breast cancer MDA-MB-231 cell line determined by in silico analyses.

Chromosoma·2025

Sex without crossovers mimics clonal reproduction in Rhynchospora tenuis.

Nature·2026

Transcriptional activity generates chromatin motion that drives nuclear blebbing.

Molecular biology of the cell·2026

Protocol for identifying head direction cells in mice using in vivo extracellular recordings and juxtacellular labeling.

STAR protocols·2026

Parallel analysis of repeat expansions: an updated Clin-CATS workflow for nanopore R10 flow cells.

The Journal of molecular diagnostics : JMD·2026

Unravelling the structure-function features of Ani2, a dual chaperone from Schizosaccharomyces pombe.

International journal of biological macromolecules·2026

Sperm subpopulations differing in mitochondrial abundance show divergent nuclear allele frequencies.

PloS one·2026

Related Experiment Videos

A system of nomenclature for band patterns of mouse chromosomes

Related Concept Videos

Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.

Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands.

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study.

The human genome project: implications for the endocrinologist.

Spectrum of MECP2 mutations in Rett syndrome.

Multi-exon deletions of the FBN1 gene in Marfan syndrome.

Sustainable integrative cell biology: CENP-C is guilty by association.

Molecular and bioinformatics analysis of long non-coding RNAs in cervical cancer.

The synaptonemal complex component corolla regulates meiotic crossover formation in Drosophila melanogaster.

Phosphorylation as a regulatory mechanism of HP1 protein multifunctionality.

RAD18 promotes cell malignant behaviors of esophageal squamous cell carcinoma by modulating ATM/STAT3/PD-L1.

Regulatory effects of lncRNA PVT1 on transcriptome in human breast cancer MDA-MB-231 cell line determined by in silico analyses.

Sex without crossovers mimics clonal reproduction in Rhynchospora tenuis.

Transcriptional activity generates chromatin motion that drives nuclear blebbing.

Protocol for identifying head direction cells in mice using in vivo extracellular recordings and juxtacellular labeling.

Parallel analysis of repeat expansions: an updated Clin-CATS workflow for nanopore R10 flow cells.

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A system of nomenclature for band patterns of mouse chromosomes

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