Related Experiment Videos
Thymidine kinase activity in individuals with galactokinase deficiency
American Journal of Human Genetics
|September 1, 1987
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Colour differences in Caucasian and Oriental women's faces illuminated by white light-emitting diode sources.
International journal of cosmetic science·2018
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males.
European journal of neurology·2013
FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome.
Clinical genetics·2011
Non-invasive measurement of local pulse pressure by pulse wave-based ultrasound manometry (PWUM).
Physiological measurement·2011
Administration of an angiotensin-converting enzyme inhibitor improves vascular function and urinary albumin excretion in low-risk essential hypertensive patients receiving anti-hypertensive treatment with calcium channel blockers. Organ-protecting effects independent of anti-hypertensive effect.
Clinical and experimental hypertension (New York, N.Y. : 1993)·2011
Expression of CD64 on polymorphonuclear neutrophils in patients with familial Mediterranean fever.
Clinical and experimental immunology·2011
The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.
American journal of human genetics·2026
Shared inheritance reveals landscape of somatic and germline cancer risk in TP53.
American journal of human genetics·2026
Examining gaps in institutional policies for clinical genomic data sharing: A cross-jurisdictional study.
American journal of human genetics·2026
Anthropometric and cardio-metabolic trait variation and genetic associations in sub-Saharan Africa.
American journal of human genetics·2026
Systematic and proactive evaluation of AIRE missense variant effects.
American journal of human genetics·2026
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.
American journal of human genetics·2026
A homozygous lamin B receptor variant resulting in Pelger-Huët anomaly without skeletal dysplasia.
Nucleus (Austin, Tex.)·2026
ZATELLITE: a toolkit to visualize and manipulate human centromeres in live cells using synthetic zinc fingers.
bioRxiv : the preprint server for biology·2026
Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.
medRxiv : the preprint server for health sciences·2026
Structural determination of human nucleosomes reconstituted by the ExACT platform.
bioRxiv : the preprint server for biology·2026
The linker histone H1.4 condenses chromatin in maturing postmitotic neurons.
bioRxiv : the preprint server for biology·2026
dif-XerCD is Required for Chromosome Segregation During cSDR-Dependent Growth in Escherichia coli.
Molecular and cellular biology·2026