about
The evolution and genomic landscape of CGB1 and CGB2 genesDifferential expression profile of growth hormone/chorionic somatomammotropin genes in placenta of small- and large-for-gestational-age newborns.Genomics and genetics of gonadotropin beta-subunit genes: Unique FSHB and duplicated LHB/CGB loci.Expression of beta-subunit of HCG genes during normal and failed pregnancy.Mid-gestational gene expression profile in placenta and link to pregnancy complications.Methylation allelic polymorphism (MAP) in chorionic gonadotropin beta5 (CGB5) and its association with pregnancy success.Structural genomic variation as risk factor for idiopathic recurrent miscarriage.Annexin A5 Promoter Haplotype M2 Is Not a Risk Factor for Recurrent Pregnancy Loss in Northern Europe.Haplotype structure of FSHB, the beta-subunit gene for fertility-associated follicle-stimulating hormone: possible influence of balancing selection.Genetics of recurrent miscarriage: challenges, current knowledge, future directions.Differential placental expression profile of human Growth Hormone/Chorionic Somatomammotropin genes in pregnancies with pre-eclampsia and gestational diabetes mellitusExtensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomesStructural and functional analysis of rare missense mutations in human chorionic gonadotrophin β-subunit.Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta.Increased placental expression and maternal serum levels of apoptosis-inducing TRAIL in recurrent miscarriage.A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage.Extensive load of somatic CNVs in the human placenta.Fine-scale quantification of HCG beta gene transcription in human trophoblastic and non-malignant non-trophoblastic tissues.Chorionic gonadotropin beta-gene variants are associated with recurrent miscarriage in two European populations.RNA sequencing of chorionic villi from recurrent pregnancy loss patients reveals impaired function of basic nuclear and cellular machinery.Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators.Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families.The Influence of Different Maternal Microbial Communities on the Development of Infant Gut and Oral Microbiota.Effects of RNA integrity on transcript quantification by total RNA sequencing of clinically collected human placental samples.WITHDRAWN: TNF-Related Apoptosis-Inducing Ligand TRAIL as a Potential Biomarker for Early Pregnancy Complications.IgG, IgA and IgM antibodies against FSH: serological markers of pathogenic autoimmunity or of normal immunoregulation?Response to "Annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?".A survey of midwives’ views on providing aspects of antenatal care in Estonia[185-POS]FSHB −211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
@nl
հետազոտող
@hy
name
Kristiina Rull
@ast
Kristiina Rull
@en
Kristiina Rull
@es
Kristiina Rull
@nl
Kristiina Rull
@sl
type
label
Kristiina Rull
@ast
Kristiina Rull
@en
Kristiina Rull
@es
Kristiina Rull
@nl
Kristiina Rull
@sl
prefLabel
Kristiina Rull
@ast
Kristiina Rull
@en
Kristiina Rull
@es
Kristiina Rull
@nl
Kristiina Rull
@sl
P1053
H-9555-2013
P106
P21
P2953
Kristiina_Rull
P31
P3829
P496
0000-0002-3396-0716