Dinucleotide repeat polymorphism at the D12S371 locus

Same author

Objective measurement of oral function in adults with spinal muscular atrophy.

Orphanet journal of rare diseases·2023

Same author

Combinatorial ASO-mediated therapy with low dose SMN and the protective modifier Chp1 is not sufficient to ameliorate SMA pathology hallmarks.

Neurobiology of disease·2022

Same author

Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies.

Revue neurologique·2020

Same author

Respiratory muscle endurance training reduces chronic neck pain: A pilot study.

Journal of back and musculoskeletal rehabilitation·2016

Same author

[Prostate biopsy: Procedure in the clinical routine].

Der Urologe. Ausg. A·2015

Same author

Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families.

Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus·2015

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 the D12S371 locus

Related Concept Videos

Objective measurement of oral function in adults with spinal muscular atrophy.

Combinatorial ASO-mediated therapy with low dose SMN and the protective modifier Chp1 is not sufficient to ameliorate SMA pathology hallmarks.

Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies.

Respiratory muscle endurance training reduces chronic neck pain: A pilot study.

[Prostate biopsy: Procedure in the clinical routine].

Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families.

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 the D12S371 locus

Related Concept Videos

Related Articles

Objective measurement of oral function in adults with spinal muscular atrophy.

Combinatorial ASO-mediated therapy with low dose SMN and the protective modifier Chp1 is not sufficient to ameliorate SMA pathology hallmarks.

Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies.

Respiratory muscle endurance training reduces chronic neck pain: A pilot study.

[Prostate biopsy: Procedure in the clinical routine].

Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families.

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.