Sequence of the putative LDL receptor binding regions of apolipoprotein B in mouse and hamster

Renal growth and development in mice lacking AT1A receptors for angiotensin II.

The American journal of physiology·1998

Imaging of oxygen saturation and distribution of erythrocytes in microvessels.

Microcirculation (New York, N.Y. : 1994)·1998

Using a reference point and videokeratography for intraoperative identification of astigmatism axis.

Journal of cataract and refractive surgery·1998

Hypertension, cardiac hypertrophy, and sudden death in mice lacking natriuretic peptide receptor A.

Proceedings of the National Academy of Sciences of the United States of America·1998

Limb, genital, CNS, and facial malformations result from gene/environment-induced cholesterol deficiency: further evidence for a link to sonic hedgehog.

American journal of medical genetics·1998

Acetylcholine-induced coronary microvascular vasospasm in a patient with angina pectoris and normal coronary angiogram--a case report.

Angiology·1997

Characterization and phylogenetic implications of the first complete mitochondrial genome of Brachylaima sp. (Digenea: Brachylaimoidea).

Gene·2026

Editor's corner: Targeting the miR-146a-3p/BDNF pathway in major depressive disorder.

Gene·2026

Genome-wide identification of the UBC protein family in grapevine and preliminary functional characterization during berry ripening.

Gene·2026

Identification of common heme-coordinating polymorphisms in human intracellular and secreted proteomes.

Gene·2026

Targeting host factors in antiviral therapy: new frontiers in combating viral infections.

Gene·2026

Dormancy and reactivation of disseminated tumor cells: From molecular mechanisms to therapeutic implications.

Gene·2026

Genetic Prioritization of Plasma Proteins Across Dementia Subtypes: A Proteome-Wide Mendelian Randomization and Bayesian Colocalization Analysis.

Cellular and molecular neurobiology·2026

Genetic covariance between plant biparental populations: concept and estimation.

Heredity·2026

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

iScience·2026

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Journal of equine science·2026

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Frontiers in medicine·2026

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

EBioMedicine·2026

Related Experiment Videos

Sequence of the putative LDL receptor binding regions of apolipoprotein B in mouse and hamster

Related Concept Videos

Renal growth and development in mice lacking AT1A receptors for angiotensin II.

Imaging of oxygen saturation and distribution of erythrocytes in microvessels.

Using a reference point and videokeratography for intraoperative identification of astigmatism axis.

Hypertension, cardiac hypertrophy, and sudden death in mice lacking natriuretic peptide receptor A.

Limb, genital, CNS, and facial malformations result from gene/environment-induced cholesterol deficiency: further evidence for a link to sonic hedgehog.

Acetylcholine-induced coronary microvascular vasospasm in a patient with angina pectoris and normal coronary angiogram--a case report.

Characterization and phylogenetic implications of the first complete mitochondrial genome of Brachylaima sp. (Digenea: Brachylaimoidea).

Editor's corner: Targeting the miR-146a-3p/BDNF pathway in major depressive disorder.

Genome-wide identification of the UBC protein family in grapevine and preliminary functional characterization during berry ripening.

Identification of common heme-coordinating polymorphisms in human intracellular and secreted proteomes.

Targeting host factors in antiviral therapy: new frontiers in combating viral infections.

Dormancy and reactivation of disseminated tumor cells: From molecular mechanisms to therapeutic implications.

Genetic Prioritization of Plasma Proteins Across Dementia Subtypes: A Proteome-Wide Mendelian Randomization and Bayesian Colocalization Analysis.

Genetic covariance between plant biparental populations: concept and estimation.

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

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Sequence of the putative LDL receptor binding regions of apolipoprotein B in mouse and hamster

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