Location of the t complex on mouse chromosome 17 by in situ hybridization with Tcp-1

Defining components of early thyroid hormone signalling through temperature-mediated activation of molecular memory in cultured Rana [lithobates] catesbeiana tadpole back skin.

General and comparative endocrinology·2023

Comparison of a PCR serotyping assay, Check&Trace assay for Salmonella, and Luminex Salmonella serotyping assay for the characterization of Salmonella enterica identified from fresh and naturally contaminated cilantro.

Food microbiology·2014

Comparison of the in vitro translation products of mRNA isolated from suspension cultures of Phaseolus vulgaris grown on maintenance and induction medium.

Planta·2014

Regulation of induction of phenylalanine ammonia-lyase in suspension cultures of Phaseolus vulgaris.

Planta·2013

Hybrid-arrested translation.

Methods in molecular biology (Clifton, N.J.)·2011

A single amino acid residue is responsible for species-specific incompatibility between CCT and alpha-actin.

FEBS letters·2009

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Immunogenetics·2026

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Immunogenetics·2026

Genetic association of immunosenescence to immune decline.

Immunogenetics·2026

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Immunogenetics·2026

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Immunogenetics·2026

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Immunogenetics·2026

Advancing genetic pathogenicity prediction with three-dimensional proteoform-phenotype analysis.

medRxiv : the preprint server for health sciences·2026

Genetic Spectrum and Family-Based Cascade Screening in Vietnamese Families With Autosomal Dominant Polycystic Kidney Disease.

Nephrology (Carlton, Vic.)·2026

Construction of an AI-Assisted Pedigree Mapping System for Hereditary Gynecological Tumors: Algorithm Development and Pilot Validation Study.

JMIR medical informatics·2026

Characteristics of predicated pathogenic missense variants in human genes for Mendelian disorders.

Frontiers in bioinformatics·2026

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia.

BMC medical genomics·2026

Punctate Palmoplantar Keratoderma Type 1 With a Multigenerational Family History: A Case Report.

Cureus·2026

Related Experiment Videos

Location of the t complex on mouse chromosome 17 by in situ hybridization with Tcp-1

Related Concept Videos

Defining components of early thyroid hormone signalling through temperature-mediated activation of molecular memory in cultured Rana [lithobates] catesbeiana tadpole back skin.

Comparison of a PCR serotyping assay, Check&Trace assay for Salmonella, and Luminex Salmonella serotyping assay for the characterization of Salmonella enterica identified from fresh and naturally contaminated cilantro.

Comparison of the in vitro translation products of mRNA isolated from suspension cultures of Phaseolus vulgaris grown on maintenance and induction medium.

Regulation of induction of phenylalanine ammonia-lyase in suspension cultures of Phaseolus vulgaris.

Hybrid-arrested translation.

A single amino acid residue is responsible for species-specific incompatibility between CCT and alpha-actin.

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Genetic association of immunosenescence to immune decline.

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Advancing genetic pathogenicity prediction with three-dimensional proteoform-phenotype analysis.

Genetic Spectrum and Family-Based Cascade Screening in Vietnamese Families With Autosomal Dominant Polycystic Kidney Disease.

Construction of an AI-Assisted Pedigree Mapping System for Hereditary Gynecological Tumors: Algorithm Development and Pilot Validation Study.

Characteristics of predicated pathogenic missense variants in human genes for Mendelian disorders.

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia.

Punctate Palmoplantar Keratoderma Type 1 With a Multigenerational Family History: A Case Report.

Related Experiment Videos

Location of the t complex on mouse chromosome 17 by in situ hybridization with Tcp-1

Related Concept Videos

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