Assignment of a type I collagen structural gene to human chromosome 7

Renal hyperparathyroidism: comparative outcomes of parathyroidectomy in two regional centres over 14 years.

Annals of the Royal College of Surgeons of England·2026

Female urethral stricture: a contemporary series.

World journal of urology·2016

Role of the biomarkers for the diagnosis of Creutzfeldt-Jakob disease.

Journal of medicine and life·2016

Molecular pathogenesis of secondary acute promyelocytic leukemia.

Mediterranean journal of hematology and infectious diseases·2011

The effect of geographic location, breed, and pituitary dysfunction on seasonal adrenocorticotropin and α-melanocyte-stimulating hormone plasma concentrations in horses.

Journal of veterinary internal medicine·2011

Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics.

Journal of medical genetics·2007

Wake-activated neuronal populations that regulate sleep drive.

Nature·2026

Observation of conformal field theory spectra in a quantum simulator.

Nature·2026

Human brain organoids record the passage of time over multiple years.

Nature·2026

Discovery of a star sensitive to the spin of Sagittarius A.

Nature·2026

Asymmetric prefrontal representations for leader-follower dynamics.

Nature·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Pediatrics international : official journal of the Japan Pediatric Society·2026

Related Experiment Videos

Assignment of a type I collagen structural gene to human chromosome 7

Related Concept Videos

Renal hyperparathyroidism: comparative outcomes of parathyroidectomy in two regional centres over 14 years.

Female urethral stricture: a contemporary series.

Role of the biomarkers for the diagnosis of Creutzfeldt-Jakob disease.

Molecular pathogenesis of secondary acute promyelocytic leukemia.

The effect of geographic location, breed, and pituitary dysfunction on seasonal adrenocorticotropin and α-melanocyte-stimulating hormone plasma concentrations in horses.

Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics.

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Observation of conformal field theory spectra in a quantum simulator.

Human brain organoids record the passage of time over multiple years.

Discovery of a star sensitive to the spin of Sagittarius A.

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Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Loci Associated With Susceptibility to Biliary Atresia-A Genome-Wide Association Study in Taiwan.

Related Experiment Videos

Assignment of a type I collagen structural gene to human chromosome 7

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