Abnormal cell lineages in mutants of the nematode Caenorhabditis elegans

Nematode postembryonic cell lineages.

Journal of nematology·2009

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

Science (New York, N.Y.)·2009

The DNA sequence and biological annotation of human chromosome 1.

Nature·2006

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia.

Neurology·2006

DNA sequence and analysis of human chromosome 9.

Nature·2004

A new class of C. elegans synMuv genes implicates a Tip60/NuA4-like HAT complex as a negative regulator of Ras signaling.

Developmental cell·2004

Botulinum toxin dysregulates calcium activity and prevents Dpp/BMP secretion from epithelial cells in the developing fly wing.

Developmental biology·2026

Consequences of losing metamorphosis on the evolution of opsin and phototransduction gene expression in the eyes of Brook Salamanders.

Developmental biology·2026

Shedding light on the proteolytically released ectodomains of membrane-bound Semaphorins.

Developmental biology·2026

NADH FLIM reveals cellular bioenergetics and mitochondrial morphology during Drosophila convergent extension.

Developmental biology·2026

Notch-regulated hematopoiesis in Drosophila: Parallels and contrasts with vertebrate blood development.

Developmental biology·2026

Limitations of serial cloning in mammals: unresolved donor-cell genomic integrity challenges broad claims of cloning limits.

Developmental biology·2026

S100 Calcium-Binding Protein 16 (S100A16) Promotes Hepatic Stellate Cell Activation Via Erb-B2 Receptor Tyrosine Kinase 2 (ERBB2)-mediated Glycolysis to Facilitate Liver Fibrosis.

Cell biochemistry and function·2026

Loss of LRRK2 Protects Against Ox-LDL-Induced Endothelial Oxidative Damage Via NRF2.

Molecular and cellular biology·2026

A Rare t(1;11)(q42;q23) Rearrangement with Trisomy 8 and Trisomy 21 in a Pediatric Acute Myeloid Leukemia Patient with Aberrant CD7 Expression and Jacob Syndrome: Diagnostic Value of Conventional Cytogenetics and Fluorescence in Situ Hybridization in a Rapidly Fatal Case.

Journal of the Association of Genetic Technologists·2026

Targeting Compensatory AKT Activation Overcomes Resistance to AXL Inhibition in Acute Lymphoblastic Leukemia.

Molecular cancer therapeutics·2026

Constructing an External Control Arm Using the French REALYSA Cohort to Replicate Outcomes of a Randomized Trial Arm in Advanced Hodgkin Lymphoma.

Clinical pharmacology and therapeutics·2026

Dynamic risk stratification using early CAR-T expansion in R/R LBCL treated with axicabtagene ciloleucel.

British journal of haematology·2026

Related Experiment Videos

Abnormal cell lineages in mutants of the nematode Caenorhabditis elegans

Related Concept Videos

Nematode postembryonic cell lineages.

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

The DNA sequence and biological annotation of human chromosome 1.

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia.

DNA sequence and analysis of human chromosome 9.

A new class of C. elegans synMuv genes implicates a Tip60/NuA4-like HAT complex as a negative regulator of Ras signaling.

Botulinum toxin dysregulates calcium activity and prevents Dpp/BMP secretion from epithelial cells in the developing fly wing.

Consequences of losing metamorphosis on the evolution of opsin and phototransduction gene expression in the eyes of Brook Salamanders.

Shedding light on the proteolytically released ectodomains of membrane-bound Semaphorins.

NADH FLIM reveals cellular bioenergetics and mitochondrial morphology during Drosophila convergent extension.

Notch-regulated hematopoiesis in Drosophila: Parallels and contrasts with vertebrate blood development.

Limitations of serial cloning in mammals: unresolved donor-cell genomic integrity challenges broad claims of cloning limits.

S100 Calcium-Binding Protein 16 (S100A16) Promotes Hepatic Stellate Cell Activation Via Erb-B2 Receptor Tyrosine Kinase 2 (ERBB2)-mediated Glycolysis to Facilitate Liver Fibrosis.

Loss of LRRK2 Protects Against Ox-LDL-Induced Endothelial Oxidative Damage Via NRF2.

A Rare t(1;11)(q42;q23) Rearrangement with Trisomy 8 and Trisomy 21 in a Pediatric Acute Myeloid Leukemia Patient with Aberrant CD7 Expression and Jacob Syndrome: Diagnostic Value of Conventional Cytogenetics and Fluorescence in Situ Hybridization in a Rapidly Fatal Case.

Targeting Compensatory AKT Activation Overcomes Resistance to AXL Inhibition in Acute Lymphoblastic Leukemia.

Constructing an External Control Arm Using the French REALYSA Cohort to Replicate Outcomes of a Randomized Trial Arm in Advanced Hodgkin Lymphoma.

Dynamic risk stratification using early CAR-T expansion in R/R LBCL treated with axicabtagene ciloleucel.

Related Experiment Videos

Abnormal cell lineages in mutants of the nematode Caenorhabditis elegans

Related Concept Videos

Related Articles