Trzeciak WH - Search Results

1

Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development.

Pereira TV, Salzano FM, Mostowska A, Trzeciak WH, Ruiz-Linares A, Chies JA, Saavedra C, Nagamachi C, Hurtado AM, Hill K, Castro-de-Guerra D, Silva-Júnior WA, Bortolini MC. Pereira TV, et al. Among authors: trzeciak wh. Proc Natl Acad Sci U S A. 2006 Apr 11;103(15):5676-81. doi: 10.1073/pnas.0509562103. Epub 2006 Apr 3. Proc Natl Acad Sci U S A. 2006. PMID: 16585527 Free PMC article.

2

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.

Mostowska A, Kobielak A, Trzeciak WH. Mostowska A, et al. Among authors: trzeciak wh. Eur J Oral Sci. 2003 Oct;111(5):365-70. doi: 10.1034/j.1600-0722.2003.00069.x. Eur J Oral Sci. 2003. PMID: 12974677 Review.

3

A novel mutation in PAX9 causes familial form of molar oligodontia.

Mostowska A, Biedziak B, Trzeciak WH. Mostowska A, et al. Among authors: trzeciak wh. Eur J Hum Genet. 2006 Feb;14(2):173-9. doi: 10.1038/sj.ejhg.5201536. Eur J Hum Genet. 2006. PMID: 16333316

4

Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia.

Mostowska A, Kobielak A, Biedziak B, Trzeciak WH. Mostowska A, et al. Among authors: trzeciak wh. Eur J Oral Sci. 2003 Jun;111(3):272-6. doi: 10.1034/j.1600-0722.2003.00036.x. Eur J Oral Sci. 2003. PMID: 12786960

5

A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?

Mostowska A, Biedziak B, Trzeciak WH. Mostowska A, et al. Among authors: trzeciak wh. J Appl Genet. 2006;47(2):159-64. doi: 10.1007/BF03194616. J Appl Genet. 2006. PMID: 16682758

6

The novel polymorphic variants within the paired box of the PAX9 gene are associated with selective tooth agenesis.

Kobielak A, Kobielak K, Wiśniewski AS, Mostowska A, Biedziak B, Trzeciak WH. Kobielak A, et al. Among authors: trzeciak wh. Folia Histochem Cytobiol. 2001;39(2):111-2. Folia Histochem Cytobiol. 2001. PMID: 11374781 Review.

7

Gene symbol: IRF6. Disease: Van der Woude syndrome.

Mostowska A, Wójcicki P, Kobus K, Trzeciak WH. Mostowska A, et al. Among authors: trzeciak wh. Hum Genet. 2005 May;116(6):534. Hum Genet. 2005. PMID: 15988826 No abstract available.

8

A novel mutation A1270G of the EDA1 gene causing Tyr343Cys substitution in ectodysplasin-A in a family with anhidrotic ectodermal dysplasia.

Kobielak A, Kobielak K, Biedziak B, Trzeciak WH. Kobielak A, et al. Among authors: trzeciak wh. Acta Biochim Pol. 2003;50(1):255-8. Acta Biochim Pol. 2003. PMID: 12673367

9

Mutation in the regulatory region of the EDA gene coincides with the symptoms of anhidrotic ectodermal dysplasia.

Kobielak K, Kobielak A, Limon J, Trzeciak WH. Kobielak K, et al. Among authors: trzeciak wh. Acta Biochim Pol. 1998;45(1):245-50. Acta Biochim Pol. 1998. PMID: 9701517

10

Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia.

Kobielak K, Kobielak A, Roszkiewicz J, Wierzba J, Limon J, Trzeciak WH. Kobielak K, et al. Among authors: trzeciak wh. Am J Med Genet. 2001 May 1;100(3):191-7. Am J Med Genet. 2001. PMID: 11343303

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