Chromosome 9qh inversions may not be true inversions

Development of a new peptide-bead coupling method for an all peptide-based Luminex multiplexing assay for detection of Plasmodium falciparum antibody responses.

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RUNX3 gene polymorphisms and haplotypes in Mexican patients with colorectal cancer.

Genetics and molecular research : GMR·2015

Effect of ZNF217 gene polymorphisms on colorectal cancer development in a Mexican population.

Genetics and molecular research : GMR·2015

p53 expression in oral lichenoid lesions and oral lichen planus.

General dentistry·2015

MDR1 C3435T polymorphism in Mexican patients with breast cancer.

Genetics and molecular research : GMR·2014

CRISPR/Cas9-based repair of a heterozygous HNF1A mutation in patient-derived hiPSCs.

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TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processing.

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The Russian FSHD registry: a first look at the cohort.

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Genetic ancestry of the Mulam ethnic group: admixture from ancient Yellow River, southern native, and Austronesian populations.

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Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension.

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α-Thalassemia in Oraons-indigenous tribal population from Jharkhand, India: insights to common deletions.

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Identification of the Novel HLA-A*68:346 Allele in a Brazilian Individual by Next-Generation Sequencing.

HLA·2026

Immunoglobulin Superfamily Protein BTNL9 Functions as a Non-Canonical Transcriptional Regulator to Suppress NSCLC Through Cell Cycle and p53 Pathways.

International journal of molecular sciences·2026

Identification of the Novel HLA-DRB1*04:01:26 Allele by Next-Generation Sequencing.

HLA·2026

The HLA-C*08:01:45 Allele, Identified by Next-Generation Sequencing in an Indian Individual.

HLA·2026

Identification of the Novel HLA-DRB1*11:01:49 Allele Using Next-Generation Sequencing in a Chinese Individual.

HLA·2026

Resolving diagnostic complexity: long-read sequencing unmasks a Hong Kongαα/‒α4.2 genotype mimicking a heterozygous ‒α3.7 deletion on multiplex ligation-dependent probe amplification.

Laboratory medicine·2026

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Chromosome 9qh inversions may not be true inversions

Related Concept Videos

Development of a new peptide-bead coupling method for an all peptide-based Luminex multiplexing assay for detection of Plasmodium falciparum antibody responses.

Short communication: Field fertility in Holstein bulls: Can type of breeding strategy (artificial insemination following estrus versus timed artificial insemination) alter service sire fertility?

RUNX3 gene polymorphisms and haplotypes in Mexican patients with colorectal cancer.

Effect of ZNF217 gene polymorphisms on colorectal cancer development in a Mexican population.

p53 expression in oral lichenoid lesions and oral lichen planus.

MDR1 C3435T polymorphism in Mexican patients with breast cancer.

CRISPR/Cas9-based repair of a heterozygous HNF1A mutation in patient-derived hiPSCs.

TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processing.

The Russian FSHD registry: a first look at the cohort.

Genetic ancestry of the Mulam ethnic group: admixture from ancient Yellow River, southern native, and Austronesian populations.

Identification of novel loci regulating circulating melatonin and its causal relationship with hypertension.

α-Thalassemia in Oraons-indigenous tribal population from Jharkhand, India: insights to common deletions.

Identification of the Novel HLA-A*68:346 Allele in a Brazilian Individual by Next-Generation Sequencing.

Immunoglobulin Superfamily Protein BTNL9 Functions as a Non-Canonical Transcriptional Regulator to Suppress NSCLC Through Cell Cycle and p53 Pathways.

Identification of the Novel HLA-DRB1*04:01:26 Allele by Next-Generation Sequencing.

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Identification of the Novel HLA-DRB1*11:01:49 Allele Using Next-Generation Sequencing in a Chinese Individual.

Resolving diagnostic complexity: long-read sequencing unmasks a Hong Kongαα/‒α4.2 genotype mimicking a heterozygous ‒α3.7 deletion on multiplex ligation-dependent probe amplification.

Related Experiment Videos

Chromosome 9qh inversions may not be true inversions

Related Concept Videos

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