Jk(a-b-) and Kidd blood group genotypes in Chinese people

Evaluating a Guideline-Integrated Clinical Interaction Framework Vs a Standard Large Language Model Interaction for Dietary Recommendations in Recurrent Urolithiasis: In Silico Study.

Journal of medical Internet research·2026

The Novel HLA-A*02:1229 Allele Was Identified by Next-Generation Sequencing.

HLA·2026

Characterisation of the Novel HLA-A02:1205 and HLA-A02:07:27 Alleles by Next-Generation Sequencing.

HLA·2026

HLA-DQB1*06:02 and a critical amino acid variant in protection against occult hepatitis B virus infection.

Frontiers in immunology·2026

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

HLA·2026

Identification of Two Novel HLA-DQB1 Alleles, HLA-DQB102:239 and HLA-DQB102:271.

HLA·2026

Optimizing blood resource allocation in Oklahoma: A geospatial analysis of available supply and potential networks of distribution.

Transfusion·2026

First molecularly characterized Para-Bombay phenotype in Iraq: Clinical, serological and genetic insights with implications for transfusion safety.

Transfusion·2026

How do I manage catastrophic failure of liquid nitrogen storage for human cells, tissues, and cellular and tissue-based products?

Transfusion·2026

Molecular characterization of CD36 deficiency in blood donors of Middle Eastern and African origin reveals transcript-level defects beyond genomic variants.

Transfusion·2026

How do we remediate blood banking/transfusion medicine fellows?

Transfusion·2026

Same-day rescue plerixafor during leukapheresis is safe and effective in allogeneic donors suboptimally responding to granulocyte colony-stimulating factor mobilization.

Transfusion·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

Jk(a-b-) and Kidd blood group genotypes in Chinese people

Related Concept Videos

Evaluating a Guideline-Integrated Clinical Interaction Framework Vs a Standard Large Language Model Interaction for Dietary Recommendations in Recurrent Urolithiasis: In Silico Study.

The Novel HLA-A*02:1229 Allele Was Identified by Next-Generation Sequencing.

Characterisation of the Novel HLA-A02:1205 and HLA-A02:07:27 Alleles by Next-Generation Sequencing.

HLA-DQB1*06:02 and a critical amino acid variant in protection against occult hepatitis B virus infection.

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

Identification of Two Novel HLA-DQB1 Alleles, HLA-DQB102:239 and HLA-DQB102:271.

Optimizing blood resource allocation in Oklahoma: A geospatial analysis of available supply and potential networks of distribution.

First molecularly characterized Para-Bombay phenotype in Iraq: Clinical, serological and genetic insights with implications for transfusion safety.

How do I manage catastrophic failure of liquid nitrogen storage for human cells, tissues, and cellular and tissue-based products?

Molecular characterization of CD36 deficiency in blood donors of Middle Eastern and African origin reveals transcript-level defects beyond genomic variants.

How do we remediate blood banking/transfusion medicine fellows?

Same-day rescue plerixafor during leukapheresis is safe and effective in allogeneic donors suboptimally responding to granulocyte colony-stimulating factor mobilization.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

Jk(a-b-) and Kidd blood group genotypes in Chinese people

Related Concept Videos

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