A centromeric microsatellite probe on chromosome 3: LIB 9-95ca (D3S1338)

The Drosophila homolog of the human tumor suppressor gene BHD interacts with the JAK-STAT and Dpp signaling pathways in regulating male germline stem cell maintenance.

Oncogene·2006

Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer.

Journal of medical genetics·2006

Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer.

Journal of medical genetics·2005

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

American journal of human genetics·2001

Oncogenic mutants of RON and MET receptor tyrosine kinases cause activation of the beta-catenin pathway.

Molecular and cellular biology·2001

The candidate tumor suppressor gene, RASSF1A, from human chromosome 3p21.3 is involved in kidney tumorigenesis.

Proceedings of the National Academy of Sciences of the United States of America·2001

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

Human molecular genetics·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.

Human molecular genetics·2026

The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.

Human molecular genetics·2026

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Human molecular genetics·2026

Simultaneous Quantification of Hundreds of Phosphorylated Metabolites in Multiple Biological Matrices with Ion-Pairing Reversed-Phase Ultrahigh-Performance Liquid Chromatography and Mass Spectrometry.

Analytical chemistry·2026

Revisiting the Fragmentation of Ketoconazole by Positive Electrospray Ionization Tandem Mass Spectrometry and Density Functional Theory Calculations.

Rapid communications in mass spectrometry : RCM·2026

Caspase-3-mediated apoptosis-associated flavor changes in large yellow croaker during cold storage induced by Pseudomonas and Acinetobacter haemolyticus: a metabolomics and headspace solid-phase microextraction-gas chromatography-mass spectrometry study.

Journal of the science of food and agriculture·2026

Glutamine synthetase deficiency triggers mitochondrial oxidative stress and a ribotoxic stress response during acute hepatic metabolic crisis.

Metabolism: clinical and experimental·2026

Multi-omics insights into aroma formation in congou black tea during fermentation.

Food chemistry·2026

Volatilomic analysis of blood and urine by headspace solid-phase microextraction gas chromatography/mass spectrometry for complementary assessment of chronic kidney disease.

Journal of pharmaceutical and biomedical analysis·2026

Related Experiment Videos

A centromeric microsatellite probe on chromosome 3: LIB 9-95ca (D3S1338)

Related Concept Videos

The Drosophila homolog of the human tumor suppressor gene BHD interacts with the JAK-STAT and Dpp signaling pathways in regulating male germline stem cell maintenance.

Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer.

Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer.

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

Oncogenic mutants of RON and MET receptor tyrosine kinases cause activation of the beta-catenin pathway.

The candidate tumor suppressor gene, RASSF1A, from human chromosome 3p21.3 is involved in kidney tumorigenesis.

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.

The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Simultaneous Quantification of Hundreds of Phosphorylated Metabolites in Multiple Biological Matrices with Ion-Pairing Reversed-Phase Ultrahigh-Performance Liquid Chromatography and Mass Spectrometry.

Revisiting the Fragmentation of Ketoconazole by Positive Electrospray Ionization Tandem Mass Spectrometry and Density Functional Theory Calculations.

Caspase-3-mediated apoptosis-associated flavor changes in large yellow croaker during cold storage induced by Pseudomonas and Acinetobacter haemolyticus: a metabolomics and headspace solid-phase microextraction-gas chromatography-mass spectrometry study.

Glutamine synthetase deficiency triggers mitochondrial oxidative stress and a ribotoxic stress response during acute hepatic metabolic crisis.

Multi-omics insights into aroma formation in congou black tea during fermentation.

Volatilomic analysis of blood and urine by headspace solid-phase microextraction gas chromatography/mass spectrometry for complementary assessment of chronic kidney disease.

Related Experiment Videos

A centromeric microsatellite probe on chromosome 3: LIB 9-95ca (D3S1338)

Related Concept Videos

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