Dinucleotide repeat polymorphism at D16S533

Same author

Recurrent MDM2 Amplification in the Spectrum of HMGA2-Altered Pleomorphic Adenoma, Atypical Pleomorphic Adenoma and Carcinoma Ex Pleomorphic Adenoma.

Head and neck pathology·2025

Same author

A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects.

Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation·2017

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

Oncogene·2017

Same author

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development.

SpringerPlus·2016

Same author

Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis.

Virchows Archiv : an international journal of pathology·2014

Same author

ENCCA WP17-WP7 consensus paper on teenagers and young adults (TYA) with bone sarcomas.

Annals of oncology : official journal of the European Society for Medical Oncology·2014

Same journal

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

Human molecular genetics·2026

Same journal

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Human molecular genetics·2026

Same journal

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Human molecular genetics·2026

Same journal

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Human molecular genetics·2026

Same journal

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Human molecular genetics·2026

Same journal

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.

Human molecular genetics·2026

Related Experiment Videos

Dinucleotide repeat polymorphism at D16S533

Related Concept Videos

Recurrent MDM2 Amplification in the Spectrum of HMGA2-Altered Pleomorphic Adenoma, Atypical Pleomorphic Adenoma and Carcinoma Ex Pleomorphic Adenoma.

A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects.

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

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development.

Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis.

ENCCA WP17-WP7 consensus paper on teenagers and young adults (TYA) with bone sarcomas.

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.

Related Experiment Videos

Dinucleotide repeat polymorphism at D16S533

Related Concept Videos

Related Articles

Recurrent MDM2 Amplification in the Spectrum of HMGA2-Altered Pleomorphic Adenoma, Atypical Pleomorphic Adenoma and Carcinoma Ex Pleomorphic Adenoma.

A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects.

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

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development.

Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis.

ENCCA WP17-WP7 consensus paper on teenagers and young adults (TYA) with bone sarcomas.

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Nicotinamide riboside prevents mitochondrial dysfunction in nemaline myopathy type 6.

Retraction: Aqua-soluble DDQ reduces the levels of Dr1 and Ab and inhibits abnormal interactions between Ab and Dr1 and protects Alzheimer's disease neurons from Ab- and Dr1-induced mitochondrial and synaptic toxicities.