Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1

Mutant p53 upregulates alpha-1 antitrypsin expression and promotes invasion in lung cancer.

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Mutant p53 drives invasion in breast tumors through up-regulation of miR-155.

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Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11.

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Systematic characterisation of the rat and human CYP24A1 promoter.

Molecular and cellular endocrinology·2010

Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis.

Journal of clinical pathology·2007

Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?

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A de novo TRPV4 variant c.2479C>G (p.Pro827Ala) in Spondylometaphyseal dysplasia Kozlowski type: identification and functional analysis.

Human molecular genetics·2026

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Human molecular genetics·2026

Fetal myogenesis chromatin state and CpG from the open alliance markers and their intersection with adult muscle and gastrointestinal genetics.

Human molecular genetics·2026

The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

Human molecular genetics·2026

A functional framework in patient fibroblasts informs ATP7A variant pathogenicity and identifies p.Q990P as a novel cause of distal motor neuropathy.

Human molecular genetics·2026

Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

Human molecular genetics·2026

Genomic landscape of Mexican patients with maturity onset diabetes of the young: beyond mutations in MODY-known genes.

Frontiers in endocrinology·2026

Linking SIRT1 gene variation and protein levels to the pathophysiology of type 2 diabetes.

Molecular biology research communications·2026

Pharmacogenetic analyses in people with dementia in Northeast Germany.

Alzheimer's & dementia (Amsterdam, Netherlands)·2026

Research progress on targeted regulatory proteins in the prevention and treatment of atherosclerosis.

Frontiers in immunology·2026

Retraction Note: Micropropagation and assessment of genetic fidelity of Dendrocalamus strictus (Roxb.) nees using RAPD and ISSR markers.

3 Biotech·2026

Distribution of ST116 carbapenem-resistant Citrobacter freundii in public genomes and characterization of a triple-carbapenemase-producing strain.

Frontiers in cellular and infection microbiology·2026

Related Experiment Videos

Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1

Related Concept Videos

Mutant p53 upregulates alpha-1 antitrypsin expression and promotes invasion in lung cancer.

Mutant p53 drives invasion in breast tumors through up-regulation of miR-155.

Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11.

Systematic characterisation of the rat and human CYP24A1 promoter.

Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis.

Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?

A de novo TRPV4 variant c.2479C>G (p.Pro827Ala) in Spondylometaphyseal dysplasia Kozlowski type: identification and functional analysis.

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Fetal myogenesis chromatin state and CpG from the open alliance markers and their intersection with adult muscle and gastrointestinal genetics.

The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

A functional framework in patient fibroblasts informs ATP7A variant pathogenicity and identifies p.Q990P as a novel cause of distal motor neuropathy.

Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

Genomic landscape of Mexican patients with maturity onset diabetes of the young: beyond mutations in MODY-known genes.

Linking SIRT1 gene variation and protein levels to the pathophysiology of type 2 diabetes.

Pharmacogenetic analyses in people with dementia in Northeast Germany.

Research progress on targeted regulatory proteins in the prevention and treatment of atherosclerosis.

Retraction Note: Micropropagation and assessment of genetic fidelity of Dendrocalamus strictus (Roxb.) nees using RAPD and ISSR markers.

Distribution of ST116 carbapenem-resistant Citrobacter freundii in public genomes and characterization of a triple-carbapenemase-producing strain.

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Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1

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