sameAs
N-acetyltransferase 8, a positional candidate for blood pressure and renal regulation: resequencing, association and in silico studyNatural antisense transcript of natriuretic peptide precursor A (NPPA): structural organization and modulation of NPPA expressionThe human ribosomal protein S7-encoding gene: isolation, structure and localization in 2p25Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskBlood pressure loci identified with a gene-centric arrayThe evolution and genomic landscape of CGB1 and CGB2 genesPharmacogenetics of follicle-stimulating hormone actionA novel snoRNA (U73) is encoded within the introns of the human and mouse ribosomal protein S3a genesSLC2A9 is a high-capacity urate transporter in humansMolecular cloning, chromosomal assignment, and expression of the mouse aspartylglucosaminidase geneGene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaGenome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1.High divergence in primate-specific duplicated regions: human and chimpanzee chorionic gonadotropin beta genesPolymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping arrayHypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.Increased Prevalance of the -211 T allele of follicle stimulating hormone (FSH) beta subunit promoter polymorphism and lower serum FSH in infertile men.Differential expression profile of growth hormone/chorionic somatomammotropin genes in placenta of small- and large-for-gestational-age newborns.HYPEST study: profile of hypertensive patients in Estonia.Genomics and genetics of gonadotropin beta-subunit genes: Unique FSHB and duplicated LHB/CGB loci.Segmental duplications and gene conversion: Human luteinizing hormone/chorionic gonadotropin beta gene cluster.No evidence of somatic DNA copy number alterations in eutopic and ectopic endometrial tissue in endometriosis.The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22.Efficient construction of a physical map by fiber-FISH of the CLN5 region: refined assignment and long-range contig covering the critical region on 13q22.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.CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T.Haplotype phasing and inheritance of copy number variants in nuclear families.Annexin A5 Promoter Haplotype M2 Is Not a Risk Factor for Recurrent Pregnancy Loss in Northern Europe.Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.Haplotype structure of FSHB, the beta-subunit gene for fertility-associated follicle-stimulating hormone: possible influence of balancing selection.Genetically determined dosage of follicle-stimulating hormone (FSH) affects male reproductive parameters.Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in EuropeansGenetics 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 mellitus
P50
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P50
description
eesti geneetik
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geneticus
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hulumtuese
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researcher
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ricercatrice
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հետազոտող
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name
Maris Laan
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Maris Laan
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Maris Laan
@es
Maris Laan
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Maris Laan
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Maris Laan
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Maris Laan
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type
label
Maris Laan
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Maris Laan
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Maris Laan
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Maris Laan
@et
Maris Laan
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Maris Laan
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Maris Laan
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altLabel
Laan M
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Maris Alver
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Maris Laan
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Maris Laan
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Maris Laan
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Maris Laan
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Maris Laan
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Maris Laan
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Maris Laan
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P1053
A-4100-2011
P1153
7004351459
P21
P214
1832149544573700490006
P2798
P2953
Maris_Laan
P31
P373
Maris Laan
P3829
P496
0000-0002-8519-243X
P569
1968-02-21T00:00:00Z
2000-01-01T00:00:00Z
P734
P735
P7859
viaf-1832149544573700490006