Literature DB >> 25992983

An interview with Sylvia Frazier-Bowers.

Sylvia Frazier-Bowers, Gustavo Zanardi, José Augusto Mendes Miguel, Rhita Almeida, Ricardo Machado Cruz.   

Abstract

Dr. Frazier-Bowers is an associate professor at the University of North Carolina, Chapel Hill (UNC-CH), in the Department of Orthodontics. She received a BA from the University of Illinois, Urbana-Champaign, and a DDS from the University of Illinois, Chicago. After completing the NIH Dentist-Scientist Program at UNC-CH in Orthodontics (Certificate, 97’) and Genetics and Molecular Biology (PhD, 99’), she completed a post-doctoral fellowship at the University of Texas Health Science Center, Houston (UTHSC), in the Department of Orthodontics. Leadership positions include president of local NC-AADR (North Carolina (2005-2006); director of the AADR Craniofacial Biology group (CBG) 2004-2007; IADR/AADR councilor for NC-AADR (2007, 2008, 2012) and for the CBG (2012-2015); member of Southern Association of Orthodontists Scientific Affairs Committee (2005-2013) and the American Association of Orthodontists Council on Scientific Affairs (2014 – Present). Dr. Frazier-Bowers also serves various editorial boards including the Journal of Dental Research and the Scientific Advisory board for the Consortium on Orthodontic Advances in Science and Technology. Her current role as faculty at UNC-CH includes conducting human genetic studies to determine the etiology of inherited tooth disorders, mentoring students at all levels, teaching graduate and pre-doctoral level Growth and Development courses and treating patients in the UNC School of Dentistry faculty practice in Orthodontics.

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Mesh:

Year:  2015        PMID: 25992983      PMCID: PMC4445221          DOI: 10.1590/2176-9451.20.2.022-028.int

Source DB:  PubMed          Journal:  Dental Press J Orthod        ISSN: 2176-9451


  11 in total

1.  Polymorphisms in the Matrilin-1 gene and risk of mandibular prognathism in Koreans.

Authors:  J Y Jang; E K Park; H M Ryoo; H I Shin; T H Kim; J S Jang; H S Park; J Y Choi; T G Kwon
Journal:  J Dent Res       Date:  2010-08-25       Impact factor: 6.116

2.  A missense mutation in DUSP6 is associated with Class III malocclusion.

Authors:  T Nikopensius; M Saag; T Jagomägi; T Annilo; M Kals; P A Kivistik; L Milani; A Metspalu
Journal:  J Dent Res       Date:  2013-08-21       Impact factor: 6.116

3.  Genetic variation in myosin 1H contributes to mandibular prognathism.

Authors:  Maria Tassopoulou-Fishell; Kathleen Deeley; Erica M Harvey; James Sciote; Alexandre R Vieira
Journal:  Am J Orthod Dentofacial Orthop       Date:  2012-01       Impact factor: 2.650

4.  Primary failure of eruption and PTH1R: the importance of a genetic diagnosis for orthodontic treatment planning.

Authors:  Sylvia A Frazier-Bowers; Darrin Simmons; J Timothy Wright; William R Proffit; James L Ackerman
Journal:  Am J Orthod Dentofacial Orthop       Date:  2010-02       Impact factor: 2.650

5.  Decrease in the expression of the type 1 PTH/PTHrP receptor (PTH1R) on chondrocytes in animals with osteoarthritis.

Authors:  Christoph Becher; Thomas Szuwart; Philipp Ronstedt; Sven Ostermeier; Adrian Skwara; Susanne Fuchs-Winkelmann; Carsten O Tibesku
Journal:  J Orthop Surg Res       Date:  2010-04-26       Impact factor: 2.359

6.  Primary failure of eruption: further characterization of a rare eruption disorder.

Authors:  Sylvia A Frazier-Bowers; Karen E Koehler; James L Ackerman; William R Proffit
Journal:  Am J Orthod Dentofacial Orthop       Date:  2007-05       Impact factor: 2.650

7.  Evidence of linkage in a Hispanic cohort with a Class III dentofacial phenotype.

Authors:  S Frazier-Bowers; R Rincon-Rodriguez; J Zhou; K Alexander; E Lange
Journal:  J Dent Res       Date:  2009-01       Impact factor: 6.116

8.  Establishing the diagnostic criteria for eruption disorders based on genetic and clinical data.

Authors:  Stephanie Golubic Rhoads; Heather M Hendricks; Sylvia A Frazier-Bowers
Journal:  Am J Orthod Dentofacial Orthop       Date:  2013-08       Impact factor: 2.650

9.  PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.

Authors:  Eva Decker; Angelika Stellzig-Eisenhauer; Britta S Fiebig; Christiane Rau; Wolfram Kress; Kathrin Saar; Franz Rüschendorf; Norbert Hubner; Tiemo Grimm; Bernhard H F Weber
Journal:  Am J Hum Genet       Date:  2008-12       Impact factor: 11.025

10.  Novel mutations in PTH1R associated with primary failure of eruption and osteoarthritis.

Authors:  S A Frazier-Bowers; H M Hendricks; J T Wright; J Lee; K Long; C F Dibble; S Bencharit
Journal:  J Dent Res       Date:  2013-12-03       Impact factor: 6.116

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