Two new types of C-band variants in human chromosome (6ph+ and 12ph+)

Cytogenetic validation of DS02R1-estimated dose for atomic bomb survivors in Hiroshima and Nagasaki with FISH.

International journal of radiation biology·2024

Chromosome aberrations do not persist in the lymphocytes or bone marrow cells of mice irradiated in utero or soon after birth.

Radiation research·2007

A method to differentiate between the levels of ESR signals induced by sunlight and by ionizing radiation in teeth from atomic bomb survivors.

Radiation research·2006

Clonally expanded T-cell populations in atomic bomb survivors do not show excess levels of chromosome instability.

Radiation research·2005

Cefoselis, a beta-lactam antibiotic, easily penetrates the blood-brain barrier and causes seizure independently by glutamate release.

Journal of neural transmission (Vienna, Austria : 1996)·2004

Human fetuses do not register chromosome damage inflicted by radiation exposure in lymphoid precursor cells except for a small but significant effect at low doses.

Radiation research·2004

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.

Jinrui idengaku zasshi. The Japanese journal of human genetics·1991

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 Clinical Nanopore Cas9-Targeted Sequencing 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

Two new types of C-band variants in human chromosome (6ph+ and 12ph+)

Related Concept Videos

Cytogenetic validation of DS02R1-estimated dose for atomic bomb survivors in Hiroshima and Nagasaki with FISH.

Chromosome aberrations do not persist in the lymphocytes or bone marrow cells of mice irradiated in utero or soon after birth.

A method to differentiate between the levels of ESR signals induced by sunlight and by ionizing radiation in teeth from atomic bomb survivors.

Clonally expanded T-cell populations in atomic bomb survivors do not show excess levels of chromosome instability.

Cefoselis, a beta-lactam antibiotic, easily penetrates the blood-brain barrier and causes seizure independently by glutamate release.

Human fetuses do not register chromosome damage inflicted by radiation exposure in lymphoid precursor cells except for a small but significant effect at low doses.

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.

Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.

The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.

The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.

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 Clinical Nanopore Cas9-Targeted Sequencing Workflow for Nanopore R10 Flow Cells.

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

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

Related Experiment Videos

Two new types of C-band variants in human chromosome (6ph+ and 12ph+)

Related Concept Videos

Related Articles