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TranscriptomicsDNA methylation profiles in the uterus during early pregnancy
Co-ordinated regulation of endometrial gene expression is essential for successful pregnancy establishment. A non-receptive uterine environment may be a key contributor to pregnancy loss, as the majority of pregnancy losses occur prior to embryo implantation. DNA methylation has been highlighted as...
ORGANISM(S): Bos taurus 
2013-05-03 | E-GEOD-43501 | biostudies-arrayexpress
MetabolomicsA Murine Model of Maternal Micronutrient Deficiencies and Gut Inflammatory Host-microbe Interactions in the Offspring.

BACKGROUND & AIMS: Micronutrient deficiency (MND) (ie, lack of vitamins and minerals) during pregnancy is a major public health concern. Historically, studies have considered micronutrients in isolation; however, MNDs rarely occur alone. The impact of co-occurring MNDs on pu...

2024-10-18 | MTBLS3476 | MetaboLights
UnknownSurvey of functional Mendelian variants in New Zealand Huntaway and Heading dog breeds.
Not available
S-EPMC12445248 | biostudies-literature
UnknownStructural and epistatic regulatory variants cause hallmark white spotting in cattle.
Not available
S-EPMC12617462 | biostudies-literature
UnknownBi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.
Not available
S-EPMC10027477 | biostudies-literature
UnknownAdd-On Treatment With Zilebesiran for Inadequately Controlled Hypertension: The KARDIA-2 Randomized Clinical Trial.
Not available
S-EPMC12120674 | biostudies-literature
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Not available
S-EPMC11291762 | biostudies-literature
UnknownBiallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities.
Not available
S-EPMC10620944 | biostudies-literature
UnknownA cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B.
Not available
S-EPMC12808965 | biostudies-literature
UnknownMutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Not available
S-EPMC5819591 | biostudies-literature
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