Dynamic mutations on the move

Same author

Effect of age in rodent models of focal and forebrain ischemia.

Stroke·1996

Same author

bcl-w, a novel member of the bcl-2 family, promotes cell survival.

Oncogene·1996

Same author

Assignment of the human GRB14 gene to chromosome 2q22-q24 by fluorescence in situ hybridization.

Genomics·1996

Same author

The effects of calcium on the thermal stability and activity of manganese peroxidase.

Archives of biochemistry and biophysics·1996

Same author

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene.

Genomics·1996

Same author

Asymptomatic large pituitary adenomas discovered at autopsy.

Surgical neurology·1996

Same journal

Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

Journal of medical genetics·2026

Same journal

Functional characterisation and pathological significance of variants of MEF2C promoter in tetralogy of Fallot.

Journal of medical genetics·2026

Same journal

Identification of biallelic loss-of-function PREP variants in three individuals with syndromic intellectual disability.

Journal of medical genetics·2026

Same journal

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Journal of medical genetics·2026

Same journal

Interpreting TP53 variants: somatic mosaicism and ERCC6L2-driven clonal evolution.

Journal of medical genetics·2026

Same journal

Review of estimates of birth incidence and population prevalence over time and between countries of the rare neurodevelopmental condition Prader-Willi syndrome.

Journal of medical genetics·2026

Related Experiment Videos

Dynamic mutations on the move

Related Concept Videos

Effect of age in rodent models of focal and forebrain ischemia.

bcl-w, a novel member of the bcl-2 family, promotes cell survival.

Assignment of the human GRB14 gene to chromosome 2q22-q24 by fluorescence in situ hybridization.

The effects of calcium on the thermal stability and activity of manganese peroxidase.

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene.

Asymptomatic large pituitary adenomas discovered at autopsy.

Longest surviving patient with a homozygous splice-altering <i>EGFR</i> pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

Functional characterisation and pathological significance of variants of <i>MEF2C</i> promoter in tetralogy of Fallot.

Identification of biallelic loss-of-function <i>PREP</i> variants in three individuals with syndromic intellectual disability.

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Interpreting <i>TP53</i> variants: somatic mosaicism and <i>ERCC6L2</i>-driven clonal evolution.

Review of estimates of birth incidence and population prevalence over time and between countries of the rare neurodevelopmental condition Prader-Willi syndrome.

Related Experiment Videos

Dynamic mutations on the move

Related Concept Videos

Related Articles

Effect of age in rodent models of focal and forebrain ischemia.

bcl-w, a novel member of the bcl-2 family, promotes cell survival.

Assignment of the human GRB14 gene to chromosome 2q22-q24 by fluorescence in situ hybridization.

The effects of calcium on the thermal stability and activity of manganese peroxidase.

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene.

Asymptomatic large pituitary adenomas discovered at autopsy.

Longest surviving patient with a homozygous splice-altering <i>EGFR</i> pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

Functional characterisation and pathological significance of variants of <i>MEF2C</i> promoter in tetralogy of Fallot.

Identification of biallelic loss-of-function <i>PREP</i> variants in three individuals with syndromic intellectual disability.

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Interpreting <i>TP53</i> variants: somatic mosaicism and <i>ERCC6L2</i>-driven clonal evolution.

Review of estimates of birth incidence and population prevalence over time and between countries of the rare neurodevelopmental condition Prader-Willi syndrome.