Pages that link to "Q81753040"
Jump to navigation
Jump to search
The following pages link to Maternal genotype affects adult offspring lipid, obesity, and diabetes phenotypes in LGXSM recombinant inbred strains (Q81753040):
Displaying 16 items.
- Evidence of maternal QTL affecting growth and obesity in adult mice (Q30439484) (← links)
- Multiple imputation of missing phenotype data for QTL mapping (Q30789398) (← links)
- Genome-wide isolation of growth and obesity QTL using mouse speed congenic strains (Q33241997) (← links)
- A maternal-offspring coadaptation theory for the evolution of genomic imprinting (Q33263582) (← links)
- A dominant X-linked QTL regulating pubertal timing in mice found by whole genome scanning and modified interval-specific congenic strain analysis (Q33363114) (← links)
- Metabolic syndrome components in murine models (Q33790395) (← links)
- Fine mapping and candidate gene search of quantitative trait loci for growth and obesity using mouse intersubspecific subcongenic intercrosses and exome sequencing. (Q34514766) (← links)
- Body composition and gene expression QTL mapping in mice reveals imprinting and interaction effects (Q34519459) (← links)
- Four out of eight genes in a mouse chromosome 7 congenic donor region are candidate obesity genes (Q35233881) (← links)
- Disentangling prenatal and postnatal maternal genetic effects reveals persistent prenatal effects on offspring growth in mice (Q35541971) (← links)
- Constraint and divergence of global gene expression in the mammalian embryo (Q35563959) (← links)
- Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides (Q35643031) (← links)
- Detecting maternal-effect loci by statistical cross-fostering (Q35917369) (← links)
- Transgenerational cardiology: One way to a baby's heart is through the mother (Q43121718) (← links)
- Dissection of a genetically complex cluster of growth and obesity QTLs on mouse chromosome 2 using subcongenic intercrosses (Q46795213) (← links)
- Innovative approach to identify multigenomic and environmental interactions associated with birth defects in family-based hybrid designs (Q100389189) (← links)