Somatic cell hybrids: applications relevant to genetic disease

X chromosome inactivation: theme and variations.

Cytogenetic and genome research·2003

Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome.

Annales de genetique·2002

Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation.

American journal of human genetics·2001

Low-copy-number human transgene is recognized as an X inactivation center in mouse ES cells, but fails to induce cis-inactivation in chimeric mice.

Genomics·2001

Severe phenotypes associated with inactive ring X chromosomes.

American journal of medical genetics·2000

Human X inactivation center induces random X chromosome inactivation in male transgenic mice.

Genomics·1999

Housing Insecurity Among Children of Incarcerated Parents in the United States.

The Journal of pediatrics·2026

Antibiotic Utilization in Medicaid-Enrolled Children: Associations with Medical Complexity.

The Journal of pediatrics·2026

Screening for Depression at Adolescent Well-Child Visits: Who Is Screened and What Happens Afterwards?

The Journal of pediatrics·2026

Children with Medical Complexity: Latent Subgroups Across Hospitalizations at Tertiary Children's Hospitals in the United States.

The Journal of pediatrics·2026

Targeted Flow Cardiac MRI in Neonates with Intracardiac Shunts: A Novel Multi-Modality Imaging Approach to Hemodynamic Assessment.

The Journal of pediatrics·2026

Neighborhood-Level Socioeconomic Disadvantage and Adverse Outcomes for Infants with Biliary Atresia in the United States.

The Journal of pediatrics·2026

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Theriogenology·2026

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Annals of the Child Neurology Society·2026

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Pain research & management·2026

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Frontiers in genetics·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Nature communications·2026

Related Experiment Videos

Somatic cell hybrids: applications relevant to genetic disease

Related Concept Videos

X chromosome inactivation: theme and variations.

Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome.

Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation.

Low-copy-number human transgene is recognized as an X inactivation center in mouse ES cells, but fails to induce cis-inactivation in chimeric mice.

Severe phenotypes associated with inactive ring X chromosomes.

Human X inactivation center induces random X chromosome inactivation in male transgenic mice.

Housing Insecurity Among Children of Incarcerated Parents in the United States.

Antibiotic Utilization in Medicaid-Enrolled Children: Associations with Medical Complexity.

Screening for Depression at Adolescent Well-Child Visits: Who Is Screened and What Happens Afterwards?

Children with Medical Complexity: Latent Subgroups Across Hospitalizations at Tertiary Children's Hospitals in the United States.

Targeted Flow Cardiac MRI in Neonates with Intracardiac Shunts: A Novel Multi-Modality Imaging Approach to Hemodynamic Assessment.

Neighborhood-Level Socioeconomic Disadvantage and Adverse Outcomes for Infants with Biliary Atresia in the United States.

Multi-omics identification of ZFPM2 and CD44 as key candidates for testicular size in sheep.

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Related Experiment Videos

Somatic cell hybrids: applications relevant to genetic disease

Related Concept Videos

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