A second generation linkage map of the human genome based on highly informative microsatellite loci

Construction and characterization of a BAC library for functional genomics in Xenopus tropicalis.

Developmental biology·2016

Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.

Prenatal diagnosis·2015

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.

Neurology·2007

The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution.

Proceedings of the National Academy of Sciences of the United States of America·2006

A SAGE approach to identifying novel trans-acting factors involved in the X inactivation process.

Cytogenetic and genome research·2006

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

Journal of medical genetics·2005

Role of estrogen receptor α in the regulation of breast cancer progression: signaling pathways and therapeutic implications.

Gene·2026

Aberrant behaviors of microRNA-142 in head and neck malignancy.

Gene·2026

MicroRNAs as novel therapeutics against multidrug-resistant ESKAPE pathogens: mechanisms, challenges, and future directions.

Gene·2026

First complete mitochondrial genome of Uzelothrips scabrosus (Thysanoptera: Uzelothripidae) provides insights into gene rearrangements and phylogenetic position within Terebrantia.

Gene·2026

RNA decay rate as a control point for long non-coding RNA function: a BRIC-based causal analysis of NEAT1.

Gene·2026

Integrative multi-omics analysis identifies an enhancer-driven ELF3-CLDN4 regulatory axis that shapes an immunosuppressive microenvironment and predicts prognosis in high-grade serous ovarian cancer.

Gene·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

A second generation linkage map of the human genome based on highly informative microsatellite loci

Related Concept Videos

Construction and characterization of a BAC library for functional genomics in Xenopus tropicalis.

Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.

The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution.

A SAGE approach to identifying novel trans-acting factors involved in the X inactivation process.

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

Role of estrogen receptor α in the regulation of breast cancer progression: signaling pathways and therapeutic implications.

Aberrant behaviors of microRNA-142 in head and neck malignancy.

MicroRNAs as novel therapeutics against multidrug-resistant ESKAPE pathogens: mechanisms, challenges, and future directions.

First complete mitochondrial genome of Uzelothrips scabrosus (Thysanoptera: Uzelothripidae) provides insights into gene rearrangements and phylogenetic position within Terebrantia.

RNA decay rate as a control point for long non-coding RNA function: a BRIC-based causal analysis of NEAT1.

Integrative multi-omics analysis identifies an enhancer-driven ELF3-CLDN4 regulatory axis that shapes an immunosuppressive microenvironment and predicts prognosis in high-grade serous ovarian cancer.

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

A second generation linkage map of the human genome based on highly informative microsatellite loci

Abstract:

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