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Displaying (1 - 8 of 8)
Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome
Placental phenotypes associated with abnormal genomic imprinting on distal mouse chromosome 7
Douglas College Human Anatomy & Physiology II
Applications of the site-specific recombinase Cre to the study of genomic imprinting
The human microbiota: The importance and relevance of its incorporation into anatomy and physiology curricula
Transcription factor ASCL2 is required for development of the glycogen trophoblast cell lineage
Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction
The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith–Wiedemann region