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Associations of folate and choline metabolism gene polymorphisms with orofacial cleftsA mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingPolymorphisms of T helper cell cytokine-associated genes and survival of hemodialysis patients - a prospective study.Involvement of 17β-hydroxysteroid dehydrogenase type gene 1 937 A>G polymorphism in infertility in Polish Caucasian women with endometriosis.Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate.T-cell cytokine gene polymorphisms and vitamin D pathway gene polymorphisms in end-stage renal disease due to type 2 diabetes mellitus nephropathy: comparisons with health status and other main causes of end-stage renal disease.Replication study for the association of seven genome- GWAS-identified Loci with susceptibility to ovarian cancer in the Polish population.Involvement of vascular endothelial growth factor -460 C/T, +405 G/C and +936 C/T polymorphisms in the development of endometriosis.Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts.Vitamin D receptor gene BsmI, FokI, ApaI and TaqI polymorphisms and the risk of systemic lupus erythematosus.Polymorphic variants in the vitamin D pathway genes and the risk of ovarian cancer among non-carriers of BRCA1/BRCA2 mutationsPolymorphisms of Vitamin D Signaling Pathway Genes and Calcium-Sensing Receptor Gene in respect to Survival of Hemodialysis Patients: A Prospective Observational StudyAssociation of the interleukin-12 polymorphic variants with the development of antibodies to surface antigen of hepatitis B virus in hemodialysis patients in response to vaccination or infection.Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients.An analysis of polymorphisms within the Wnt signaling pathway in relation to ovarian cancer risk in a Polish population.A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.De novo EDA mutations: Variable expression in two Egyptian families.Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population.Antibodies to HBV surface antigen in relation to interferon-λ3 in hemodialysis patients.Polymorphic variants in the dopamine receptor D2 in women with endometriosis-related infertility.Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population.EVC gene polymorphisms and risks of isolated hypospadias - a preliminary study.Association investigation of BACH2 rs3757247 and SOD2 rs4880 polymorphisms with the type 1 diabetes and diabetes long-term complications risk in the Polish population.Polymorphic variants of genes related to arginine metabolism and the risk of orofacial clefts.Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.Folate and choline metabolism gene variants and development of uterine cervical carcinoma.Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate.IL4R and IL13 polymorphic variants and development of antibodies to surface antigen of hepatitis B virus in hemodialysis patients in response to HBV vaccination or infection.Polymorphic variants of DNMT3A and the risk of endometriosis.Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.Circulating Interferon-λ3, Responsiveness to HBV Vaccination, and HBV/HCV Infections in Haemodialysis Patients.GREM2 nucleotide variants and the risk of tooth agenesis.Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate.Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate.Association of common variants in PAH and LAT1 with non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Polish population.Further Evidence of the Association of the Diacylglycerol Kinase Kappa (DGKK) Gene With Hypospadias.Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palate.Association of aldosterone synthase (CYP11B2) gene -344T/C polymorphism with the risk of primary chronic glomerulonephritis in the Polish population.Involvement of adropin and adropin-associated genes in metabolic abnormalities of hemodialysis patients.Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.
P50
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P50
description
researcher
@en
name
Adrianna Mostowska
@en
Adrianna Mostowska
@nl
type
label
Adrianna Mostowska
@en
Adrianna Mostowska
@nl
prefLabel
Adrianna Mostowska
@en
Adrianna Mostowska
@nl
P106
P31
P496
0000-0003-4181-9402