O-083. Parental imprinting in normal and abnormal growth

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Genetic conflict in early development: parental imprinting in normal and abnormal growth.

Parental (genomic) imprinting is the process by which the differential expression of maternal and paternal alleles at certain genetic loci in mammalian embryos occurs. Such loci are implicated in the control of fetal, placental and neonatal growth, and, more generally, in diverse aspects of fetal nutrient acquisition and maternal-fetal interactions. Not surprisingly, the aberrant expression of ...

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Parental genomic imprinting in endocrinopathies.

Genomic imprinting is the phenomenon whereby some genes preferentially produce mRNA transcripts from the gene copy derived from the parent of a specific sex. It has been implicated in a number of human diseases (most of them of endocrine interest), such as Prader-Willi/Angelman syndromes, Silver-Russell syndrome, Beckwith-Wiedemann syndrome, transient neonatal diabetes, the focal form of nesidi...

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.................................................................................... 5 ABBREVIATIONS .......................................................................... 7 FOREWORD ................................................................................... 9 INTRODUCTION .......................................................................... 10 GENERAL ASPECTS ON GROWTH REGULAT...

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Normal Abnormal Normal Abnormal

reference electrode (3). The ionized calcium concentration of sequential retentates prepared by ultrafiltration of a human control serum increased with increasing protein concentration in a way consistent with Donnan theory (4, 5) when the analyzers’ standard reference-electrode liquid junctionswere used; however, the ionized calcium in the same retentates declined slightly with increasing prot...

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ژورنال

عنوان ژورنال: Human Reproduction

سال: 1999

ISSN: 1460-2350,0268-1161

DOI: 10.1093/humrep/14.suppl_3.45-a