Genetic complementation analysis in somatic cell hybrids of alpha-L-iduronidase deficient cells

X-linked Emery-Dreifuss muscular dystrophy with lamin A deficiency and IBM inclusions.

Clinical neuropathology·2010

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.

Muscle & nerve·2004

[Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures].

Der Nervenarzt·2002

Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues.

Cytogenetics and cell genetics·2002

Both emerin and lamin C depend on lamin A for localization at the nuclear envelope.

Journal of cell science·2001

The cyo operon of Pseudomonas putida is involved in carbon catabolite repression of phenol degradation.

Molecular genetics and genomics : MGG·2001

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

Human genetics·2026

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

Human genetics·2026

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

Human genetics·2026

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

Human genetics·2026

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

Human genetics·2026

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

Human genetics·2026

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat.

Journal of clinical laboratory analysis·2026

HIPK4 is a novel gene associated with teratozoospermia and male infertility.

Human reproduction open·2026

Edge Preserved U-Net for chromosome edge detection.

Computational biology and chemistry·2026

A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

International journal of molecular sciences·2026

Circadian Disruption Is Associated with Elevated Whole-Semen mtDNA Copy Number and Implicates CRY1 as a Candidate Regulator in Humans and Mice.

International journal of molecular sciences·2026

A single-cell multi-omic atlas of the human pancreas reveals potential for cellular plasticity across development, health, and disease.

Cell metabolism·2026

Related Experiment Videos

Genetic complementation analysis in somatic cell hybrids of alpha-L-iduronidase deficient cells

Related Concept Videos

X-linked Emery-Dreifuss muscular dystrophy with lamin A deficiency and IBM inclusions.

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.

[Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures].

Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues.

Both emerin and lamin C depend on lamin A for localization at the nuclear envelope.

The cyo operon of Pseudomonas putida is involved in carbon catabolite repression of phenol degradation.

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.

Clinical and Cytogenomic Characterization of Three Patients With Distal 1q43q44 Deletion: Twin Sisters With a de novo Deletion and a Patient With der(1)t(1;21)(q43;q22.3)mat.

HIPK4 is a novel gene associated with teratozoospermia and male infertility.

Edge Preserved U-Net for chromosome edge detection.

A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

Circadian Disruption Is Associated with Elevated Whole-Semen mtDNA Copy Number and Implicates CRY1 as a Candidate Regulator in Humans and Mice.

A single-cell multi-omic atlas of the human pancreas reveals potential for cellular plasticity across development, health, and disease.

Related Experiment Videos

Genetic complementation analysis in somatic cell hybrids of alpha-L-iduronidase deficient cells

Related Concept Videos

Related Articles