Stch maps to mouse chromosome 16, extending the conserved synteny with human chromosome 21

Detailed analysis of a 17q21 microdissection library by sequence bioinformatics and isolation of region-specific clones.

Somatic cell and molecular genetics·1998

Assignment of three human markers in chromosome 21q11 to mouse chromosome 16.

Somatic cell and molecular genetics·1998

Characterization and localization of Mox2, the gene encoding the murine homolog of the rat MRC OX-2 membrane glycoprotein.

Mammalian genome : official journal of the International Mammalian Genome Society·1998

The affected gene underlying the class K glycosylphosphatidylinositol (GPI) surface protein defect codes for the GPI transamidase.

Proceedings of the National Academy of Sciences of the United States of America·1997

Specificity of attachment and neurite outgrowth of dissociated basal forebrain cholinergic neurons seeded on to organotypic slice cultures of forebrain.

Neuroscience·1997

Infections in craniofacial surgery: a combined report of 567 procedures from two centers.

Plastic and reconstructive surgery·1997

Exploring differences across pangenome-graph representations using Escherichia coli O157:H7 as a model.

Genomics·2026

Comprehensive analysis of differentially expressed mRNAs, lncRNAs, and miRNAs involved in ovarian differentiation and development in Qihe gibel carp (Carassius gibelio var. Qihe).

Genomics·2026

Genome-wide association and selective sweep analyses reveal genetic loci for teat number trait in pigs.

Genomics·2026

Effects of domestication on the body morphology and genetic diversity of the yellowfin seabream (Acanthopagrus latus).

Genomics·2026

A muskrat tissue atlas of small non-coding RNAs and their regulatory roles in muskrat musk secretion.

Genomics·2026

Dynamic transcriptomic landscape from bulk RNA-seq reveals critical mmu-miR-181a-5p/hif1a and mmu-miR-101a-3p/col1a1 modules for deep second-degree burn wound healing.

Genomics·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

Stch maps to mouse chromosome 16, extending the conserved synteny with human chromosome 21

Related Concept Videos

Detailed analysis of a 17q21 microdissection library by sequence bioinformatics and isolation of region-specific clones.

Assignment of three human markers in chromosome 21q11 to mouse chromosome 16.

Characterization and localization of Mox2, the gene encoding the murine homolog of the rat MRC OX-2 membrane glycoprotein.

The affected gene underlying the class K glycosylphosphatidylinositol (GPI) surface protein defect codes for the GPI transamidase.

Specificity of attachment and neurite outgrowth of dissociated basal forebrain cholinergic neurons seeded on to organotypic slice cultures of forebrain.

Infections in craniofacial surgery: a combined report of 567 procedures from two centers.

Exploring differences across pangenome-graph representations using Escherichia coli O157:H7 as a model.

Comprehensive analysis of differentially expressed mRNAs, lncRNAs, and miRNAs involved in ovarian differentiation and development in Qihe gibel carp (Carassius gibelio var. Qihe).

Genome-wide association and selective sweep analyses reveal genetic loci for teat number trait in pigs.

Effects of domestication on the body morphology and genetic diversity of the yellowfin seabream (Acanthopagrus latus).

A muskrat tissue atlas of small non-coding RNAs and their regulatory roles in muskrat musk secretion.

Dynamic transcriptomic landscape from bulk RNA-seq reveals critical mmu-miR-181a-5p/hif1a and mmu-miR-101a-3p/col1a1 modules for deep second-degree burn wound healing.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

Stch maps to mouse chromosome 16, extending the conserved synteny with human chromosome 21

Related Concept Videos

Related Articles