Adrianna Mostowska

Summary

Affiliation: Medical University
Country: Poland

Publications

  1. doi Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 94:943-50. 2012
  2. doi Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Arch Oral Biol 57:790-5. 2012
  3. doi Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 120:1-8. 2012
  4. doi Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poland
    Birth Defects Res A Clin Mol Teratol 88:538-45. 2010
  5. doi Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 91:948-55. 2011
  6. doi Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 94:42-6. 2012
  7. doi Polymorphisms in CHDH gene and the risk of tooth agenesis
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 91:169-76. 2011
  8. doi Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 118:325-32. 2010
  9. doi Associations of folate and choline metabolism gene polymorphisms with orofacial clefts
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, Poznan, Poland
    J Med Genet 47:809-15. 2010
  10. ncbi Polymorphic variants of genes encoding main antioxidant enzymes and the risk of CL/P-affected pregnancies
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences in Poznan, Swiecickiego St 6, 60 781 Poznan, Poland
    Clin Biochem 40:416-9. 2007

Collaborators

  • Margarita Lianeri
  • Paweł P Jagodziński
  • Piotr Wojcicki
  • Anna Sowińska
  • Anna Dabrowska
  • Joanna Hauser
  • K K Hozyasz
  • Aleksandra Szczepankiewicz
  • Alicja E Grzegorzewska
  • Malgorzata Szczepanska
  • Wojciech Warchoł
  • Agnieszka Gaczkowska
  • Malgorzata Wegner
  • Przemyslaw Wirstlein
  • Jana Skrzypczak
  • Matthew Misztal
  • Piotr M Wobszal
  • Piotr Pawlik
  • Andrzej Roszak
  • Magdalena Mostowska
  • Tiago V Pereira
  • Bartosz Kempisty
  • Ebtesam M Abdalla
  • Ireneusz Stolarek
  • Ghada M Elhady
  • Mateusz Paciorkowski
  • Marek Figlerowicz
  • Monika K Świderska
  • Karin M L Dowidar
  • Bartosz Frycz
  • Magdalena Polcyn-Adamczak
  • Mahua Choudhury
  • Dorota Zozulinska-Ziolkiewicz
  • Bogna Wierusz-Wysocka
  • Maria Piorunska-Stolzmann
  • Aleksandra Araszkiewicz
  • Paulina Zielinska
  • Zofia Niemir
  • Grzegorz Ostromecki
  • Magdalena Pawlik
  • Dominik Pajzderski
  • Stefan Sajdak
  • A Kobielak
  • Helena Kedzia
  • Andrzej Oko
  • Wieslaw H Trzeciak
  • Francisco M Salzano
  • Marta Łuczak
  • Cleusa Nagamachi
  • Maria Catira Bortolini
  • Carmen Saavedra
  • Piotr Czerski
  • Ilona Górska
  • Wilson A Silva-Junior
  • Andres Ruiz-Linares
  • Dinorah Castro-de-Guerra
  • Ana M Hurtado
  • Kim Hill
  • José A B Chies
  • B Biedziak
  • W H Trzeciak
  • A S Wisniewski
  • K Kobielak

Detail Information

Publications45

  1. doi Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 94:943-50. 2012
    ....
  2. doi Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Arch Oral Biol 57:790-5. 2012
    ..The aim of the study was to search for casual mutations underlying hypodontia in a family with agenesis of the second premolars and third molars...
  3. doi Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 120:1-8. 2012
    ..In conclusion, our study confirmed the involvement of polymorphisms in the WNT3 gene in NCL/P aetiology in the tested population...
  4. doi Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poland
    Birth Defects Res A Clin Mol Teratol 88:538-45. 2010
    ..Because of the genetic heterogeneity of facial clefts, the aim of this study was to investigate the contribution of previously reported candidate genes and chromosomal loci to the risk of CL/P in the Polish population...
  5. doi Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 91:948-55. 2011
    ..It has been shown that maternal psychological stress in the periconceptional period can contribute to an increase in the risk of NCL/P affecting pregnancy...
  6. doi Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 94:42-6. 2012
    ..Therefore, the objective of this report was to investigate the contribution of the top seven polymorphisms reaching genome-wide statistical significance in GWAS analyses in the Polish population...
  7. doi Polymorphisms in CHDH gene and the risk of tooth agenesis
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 91:169-76. 2011
    ..The purpose of this study was to evaluate the possibility that polymorphic variants of genes encoding the main folate and choline metabolism enzymes might be associated with the risk of hypodontia in the Polish population...
  8. doi Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 118:325-32. 2010
    ..Altogether, our study identified a novel gene, the nucleotide variants of which were be associated with a decreased risk of having a baby with NCL/P...
  9. doi Associations of folate and choline metabolism gene polymorphisms with orofacial clefts
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, Poznan, Poland
    J Med Genet 47:809-15. 2010
    ..It has been reported that maternal nutritional factors are likely to play a major role in development of NCL/P in the embryo...
  10. ncbi Polymorphic variants of genes encoding main antioxidant enzymes and the risk of CL/P-affected pregnancies
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences in Poznan, Swiecickiego St 6, 60 781 Poznan, Poland
    Clin Biochem 40:416-9. 2007
    ..The study focused on the correlation between maternal polymorphisms of genes encoding antioxidant enzymes and the risk of having a child with CL/P in the Polish population...
  11. ncbi Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population
    A Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences in Poznan, Poznan, Poland
    Clin Genet 69:512-7. 2006
    ..Our observations are consistent with a significant role of the methyl cycle in the development of craniofacial structures in humans...
  12. ncbi A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, Swiecickiego 6, 60 781 Poznan, Poland
    J Appl Genet 47:159-64. 2006
    ..It may also support the view that this common anomaly of human dentition might be an oligogenic trait caused by simultaneous mutations of different genes...
  13. ncbi Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences in Poznan, Swiecickiego St 6, 60 781 Poznan, Poland
    J Hum Genet 51:262-6. 2006
    ..This alternation may negatively affect the splicing process and cellular concentration of AXIN2 protein. Our findings suggest that AXIN2 polymorphic variants may be associated with both hypodontia and oligodontia...
  14. ncbi A novel mutation in PAX9 causes familial form of molar oligodontia
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, Poznan, Poland
    Eur J Hum Genet 14:173-9. 2006
    ..Our results support the view that mutations in PAX9 constitute a causative factor in nonsyndromic oligodontia...
  15. ncbi Gene symbol: IRF6. Disease: Van der Woude syndrome
    A Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences in Poznan, Poland
    Hum Genet 116:534. 2005
  16. doi Folate and choline metabolism gene variants and development of uterine cervical carcinoma
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, 6 Swiecickiego St, 60 781 Poznan, Poland
    Clin Biochem 44:596-600. 2011
    ..The aim of this study was to evaluate the possibility that polymorphic variants of genes that may affect DNA methylation status are associated with the risk of cervical cancer in the Polish population...
  17. pmc Association 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
    Alicja E Grzegorzewska
    Department of Nephrology, Transplantology and Internal Diseases, Poznan University of Medical Sciences, 49 Przybyszewskiego Blvd, 60 355, Poznan, Poland
    Mol Biol Rep 40:6899-911. 2013
    ....
  18. pmc Association of Retinoid X Receptor Alpha Gene Polymorphism with Clinical Course of Chronic Glomerulonephritis
    Alicja E Grzegorzewska
    Department of Nephrology, Transplantology and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland
    Med Sci Monit 21:3671-81. 2015
    ..004, Pgenotype=0.008). CONCLUSIONS RXRA rs10776909 allele T is specifically involved in the pathogenesis of ChGN. This risk allele may be also associated with worse clinical course of ChGN. ..
  19. doi Novel PAX9 mutation associated with syndromic tooth agenesis
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 121:403-11. 2013
    ..In conclusion, the novel PAX9 deletion might be responsible for tooth agenesis and trichodysplasia in the investigated family. This c.59delC mutation potentially leads to PAX9 transcription factor haploinsufficiency. ..
  20. pmc DNMT1, DNMT3A and DNMT3B gene variants in relation to ovarian cancer risk in the Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, 6 Swiecickiego Street, 60 781, Poznan, Poland
    Mol Biol Rep 40:4893-9. 2013
    ..Our results may suggest that DNMT1 variants may be risk factors of ovarian cancer...
  21. pmc Vitamin D receptor gene BsmI and FokI polymorphisms in relation to ovarian cancer risk in the Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Genet Test Mol Biomarkers 17:183-7. 2013
    ..The role of vitamin D receptor (VDR) single-nucleotide polymorphisms (SNPs) in ovarian cancer has been studied in various populations; however, these results are discordant between different ethnicities...
  22. ncbi Association of 677C>T polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene with bipolar disorder and schizophrenia
    Bartosz Kempisty
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, 6 Swiecickiego St, 60 781 Poznan, Poland
    Neurosci Lett 400:267-71. 2006
    ..393; 95% CI=1.429-4.006; P=0.0008 and OR=2.036; 95% CI=1.207-3.433; P=0.0073, respectively). This finding indicates possible association of BD and schizophrenia with the 1p36.3 MTHFR locus...
  23. ncbi Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 111:365-70. 2003
    ..This paper aims to review current literature about the molecular mechanisms responsible for selective tooth agenesis in humans...
  24. doi Association between DNMT3L polymorphic variants and the risk of endometriosis-associated infertility
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznań 60 781, Poland
    Mol Med Rep 13:1040-6. 2016
    ..On the basis of these results, the present study has demonstrated that variations in the DNMT3L gene do not contribute to stage I-II endometriosis-associated infertility...
  25. doi Folate and choline metabolism gene variants in relation to ovarian cancer risk in the Polish population
    Piotr Pawlik
    Clinic of Gynecological Surgery, Poznan University of Medical Sciences, Poznan, Poland
    Mol Biol Rep 39:5553-60. 2012
    ..Our results might suggest that the selected polymorphic gene variants may not contribute to ovarian cancer incidence...
  26. ncbi Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, Swiecickiego Str 6, PL 60 781 Poznan, Poland
    Eur J Oral Sci 111:272-6. 2003
    ..Our results support the view that mutations in PAX9 could constitute a causative factor of oligodontia. We hypothesize that the G151A transition in PAX9 might be responsible for the sporadic form of tooth agenesis in this patient...
  27. doi Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 100:670-8. 2014
    ..Given the critical role of DNA damage repair in the embryonic development, we decided to test the hypothesis that polymorphisms of selected DNA repair genes might contribute to the risk of NSCL/P in the Polish population...
  28. ncbi Contribution of IL12A and IL12B polymorphisms to the risk of cervical cancer
    Andrzej Roszak
    Department of Radiotherapy and Gynecological Oncology, Greater Poland Cancer Centre Poznan, Poznan, Poland
    Pathol Oncol Res 18:997-1002. 2012
    ..Our studies confirmed that the IL12B 3'UTR A>C polymorphism may be a genetic risk factor for cervical cancer...
  29. doi No association of monocyte chemoattractant protein-1 -2518 A/G polymorphism with the risk of primary glomerulonephritis in the Polish population
    Magdalena Mostowska
    Department of Nephrology, Transplantology and Internal Medicine, Poznan University of Medical Sciences, 49 Przybyszewskiego St, 60355, Poznan, Poland
    Mol Biol Rep 39:5933-41. 2012
    ..Our observations indicate that the MCP-1 -2518 A > G and C1GalT1 1365 A > G polymorphisms might not be a risk factor in the incidence of primary GN in the Polish population...
  30. doi Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Birth Defects Res A Clin Mol Teratol 103:847-56. 2015
    ..The aim of the present study was to find the GREM1 functional variants implicated in the aetiology of this common developmental anomaly in the Polish population...
  31. doi Polymorphic variants in vitamin D signaling pathway genes and the risk of endometriosis-associated infertility
    Malgorzata Szczepanska
    Department of Obstetrics, Gynecology and Gynecological Oncology, Division of Reproduction, Poznan University of Medical Sciences, Poznań 60 781, Poland
    Mol Med Rep 12:7109-15. 2015
    ..659 (1.122‑2.453), P=0.011]. The results of the present study suggested that VDR gene variants act as genetic risk factors for endometriosis‑associated infertility...
  32. doi 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
    Alicja E Grzegorzewska
    Department of Nephrology, Transplantology and Internal Diseases, Poznan University of Medical Sciences, 49 Przybyszewskiego Blvd, Poznan 60 355, Poland
    Vaccine 31:1766-70. 2013
    ..8%, CC 3.8%; IL13 CC 60.5%, CT 34.6%, TT 4.9%). In HD patients, neither the IL4R nor IL13 polymorphism is associated with anti-HBs development irrespective of whether an immunization is provoked by HBV vaccination or HBV infection...
  33. pmc Polymorphic variants in the vitamin D pathway genes and the risk of ovarian cancer among non-carriers of BRCA1/BRCA2 mutations
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznań 60 781, Poland
    Oncol Lett 11:1181-1188. 2016
    ..004; Pcorr=0.032). In conclusion, this study demonstrated that certain VDR and RXRA SNPs may be risk factors for OC in non-carriers of BRCA1/BRCA2 mutations in the Polish population...
  34. pmc Replication study for the association of seven genome- GWAS-identified Loci with susceptibility to ovarian cancer in the Polish population
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, 6 Swiecickiego St, 60 781, Poznan, Poland
    Pathol Oncol Res 21:307-13. 2015
    ..532 (95% CI = 0.342 - 0.827, p = 0.005, p(corr) = 0.035). Despite the relatively small sample size of cases and controls, our studies confirmed some of the previously-demonstrated GWAS SNPs as genetic risk factors for EOTs...
  35. pmc Vitamin D receptor gene BsmI, FokI, ApaI and TaqI polymorphisms and the risk of systemic lupus erythematosus
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, 6 Swiecickiego St, 60 781, Poznan, Poland
    Mol Biol Rep 40:803-10. 2013
    ..Our study indicates that the studied VDR FokI variant might increase the risk of some clinical presentations in patients with SLE...
  36. pmc Polymorphisms of Vitamin D Signaling Pathway Genes and Calcium-Sensing Receptor Gene in respect to Survival of Hemodialysis Patients: A Prospective Observational Study
    Alicja E Grzegorzewska
    Chair and Department of Nephrology, Transplantology and Internal Diseases, Poznan University of Medical Sciences, Przybyszewskiego 49, 60 355 Poznan, Poland
    Int J Endocrinol 2016:2383216. 2016
    ..59, 95% CI 0.37-0.96, P = 0.04). In conclusion, GC rs2298849 and VDR rs2228570 SNPs are associated with survival on HD. VDR-related cardiovascular mortality may occur due to connections of rs2228570 with dyslipidemia. ..
  37. doi WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies
    Adrianna Mostowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Eur J Oral Sci 123:1-8. 2015
    ..In conclusion, this is the first report implicating coding variants in the WNT10A gene in the aetiology of MLIA. These results will require further confirmation using larger-scale studies...
  38. pmc Antibodies to hepatitis B virus surface antigen and interleukin 12 and interleukin 18 gene polymorphisms in hemodialysis patients
    Alicja E Grzegorzewska
    Department of Nephrology, Transplantology and Internal Diseases, Poznan University of Medical Sciences, 49 Przybyszewskiego Blvd, 60 355 Poznan, Poland
    BMC Nephrol 13:75. 2012
    ..We studied whether polymorphisms in the IL12A 3` untranslated region (UTR) and IL12B 3`UTR may contribute to anti-HBs development (titre ≥ 10 IU/L) in HD patients either individually or jointly with the IL18 polymorphism...
  39. pmc Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients
    Alicja E Grzegorzewska
    Department of Nephrology, Transplantology and Internal Diseases, Poznan University of Medical Sciences, Poznan, Poland
    Sci Rep 6:35188. 2016
    ..According to computational analysis, potential binding sites for GLI3, AHR and TP53 are removed by the A allele, whereas binding sites for SOX18 and TP63 are created...
  40. pmc Association investigation of BACH2 rs3757247 and SOD2 rs4880 polymorphisms with the type 1 diabetes and diabetes long-term complications risk in the Polish population
    Malgorzata Wegner
    Lipid Metabolism Laboratory, Department of General Chemistry, Chemistry and Clinical Biochemistry, Poznan University of Medical Sciences, Poznan 60 780, Poland
    Biomed Rep 3:327-332. 2015
    ..The present study did not confirm the involvement of BACH2 rs3757247 and SOD2 rs4880 polymorphisms in the development of DM1 and diabetes long-term complications. Further studies in a larger population sample are required...
  41. doi De novo EDA mutations: Variable expression in two Egyptian families
    Agnieszka Gaczkowska
    Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland
    Arch Oral Biol 68:21-8. 2016
    ....
  42. doi Polymorphic variants in the dopamine receptor D2 in women with endometriosis-related infertility
    Malgorzata Szczepanska
    Department of Obstetrics, Gynecology and Gynecological Oncology, Division of Reproduction, Poznan University of Medical Sciences, Poznań 60 781, Poland
    Mol Med Rep 12:3055-60. 2015
    ..The present results did not confirm DRD2 gene variants to be genetic risk factors for endometriosis-related infertility...
  43. ncbi The novel polymorphic variants within the paired box of the PAX9 gene are associated with selective tooth agenesis
    A Kobielak
    Department of Biochemistry and Molecular Biology, University of Medical Sciences, Poznan, Poland
    Folia Histochem Cytobiol 39:111-2. 2001
    ..However, this polymorphism does not alter amino acid sequence of the protein product of this gene...
  44. ncbi [Genetic polymorphisms of GSTM1 and GSTT1 in mothers of children with isolated cleft lip with or without cleft palate]
    Kamil K Hozyasz
    Kilinika Pediatrii, Instytut Matki i Dziecka, Warszawa
    Przegl Lek 62:1019-22. 2005
    ..Our results suggest that homozygous deletions of GSTM1 and GSTT1 in mother genome might increase the risk of having child with cleft lip with or without cleft palate...
  45. pmc Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development
    Tiago V Pereira
    Departamento de Genetica, Instituto de Biociencias, Universidade Federal do Rio Grande do Sul, Caixa Postal 15053, 91501 970 Porto Alegre, Brazil
    Proc Natl Acad Sci U S A 103:5676-81. 2006
    ..New World and Old World primate lineages may, however, have different degrees of restriction for changes in this DNA region...