The Habbanite isolate. I. Genetic markers in the blood

Typing of normal and variant red cells with ABO, Rh, and Kell typing reagents using a gel typing system.

Immunohematology·1991

Comparison of the reactions of the Rh-related murine monoclonal antibodies BS58 and R6A.

Vox sanguinis·1990

PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system.

Human genetics·1987

Genetic polymorphisms among Ethiopian Jews in Israel.

Gene geography : a computerized bulletin on human gene frequencies·1987

The isolation and characterisation of a putative adipocyte precursor cell type from the white adipose tissue of the chicken (Gallus domesticus).

Comparative biochemistry and physiology. A, Comparative physiology·1987

Identification and partial characterization of the human erythrocyte membrane component(s) that express the antigens of the LW blood-group system.

The Biochemical journal·1986

A frequentist test of proportional colocalization after selecting relevant genetic variants.

Human heredity·2026

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Human heredity·2026

Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

Human heredity·2026

Erratum.

Human heredity·2026

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Human heredity·2025

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

Human heredity·2025

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Related Experiment Videos

The Habbanite isolate. I. Genetic markers in the blood

Related Concept Videos

Typing of normal and variant red cells with ABO, Rh, and Kell typing reagents using a gel typing system.

Comparison of the reactions of the Rh-related murine monoclonal antibodies BS58 and R6A.

PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system.

Genetic polymorphisms among Ethiopian Jews in Israel.

The isolation and characterisation of a putative adipocyte precursor cell type from the white adipose tissue of the chicken (Gallus domesticus).

Identification and partial characterization of the human erythrocyte membrane component(s) that express the antigens of the LW blood-group system.

A frequentist test of proportional colocalization after selecting relevant genetic variants.

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

Erratum.

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Related Experiment Videos

The Habbanite isolate. I. Genetic markers in the blood

Related Concept Videos

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