Genomes and Genes
J K Hartsfield
Affiliation: Indiana University
- Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smokingJ K Hartsfield
Oral Facial Genetics Section, Indiana University School of Dentistry, Indianapolis, Indiana 46202 5186, USA
Am J Med Genet 102:21-4. 2001..This suggests that when mothers smoke periconceptionally, their infants having these alleles at either (or both) loci were not at substantially increased risk for CL/P compared to infants with the wild-type alleles...
- Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia)J K Hartsfield
Department of Orthodontics and Oral Facial Genetics, Indiana University School of Dentistry, Indianapolis, IN, USA
Orthod Craniofac Res 10:121-8. 2007..The same genetic-environmental factors and or etiological mechanisms may then be investigated in apparently sporadic cases...
- The Ephx1(d) allele encoding an Arg338Cys substitution is associated with heat labilityJ K Hartsfield
Oral Facial Genetics Program, Department of Oral Facial Development, Indiana University School of Dentistry, 1121 W Michigan Street, DS270, Indianapolis, Indiana 46202, USA
Mamm Genome 11:915-8. 2000..5cm (lod = 10.0)...
- Root resorption associated with orthodontic force in IL-1Beta knockout mouseR A Al-Qawasmi
Indiana University School of Dentistry, Indianapolis, IN 46202, USA
J Musculoskelet Neuronal Interact 4:383-5. 2004
- Assignment1 of microsomal epoxide hydrolase (EPHX1) to human chromosome 1q42.1 by in situ hybridizationJ K Hartsfield
Division of Oral Facial Genetics, Indiana University School of Dentistry, Indianapolis IN, USA
Cytogenet Cell Genet 83:44-5. 1998
- Genetic predisposition to external apical root resorption in orthodontic patients: linkage of chromosome-18 markerR A Al-Qawasmi
Department of Oral Facial Development, Indiana University School of Dentistry, 1121 West Michigan Street, Indianapolis 46202 5186, USA
J Dent Res 82:356-60. 2003..5; p = 0.02) of EARR affecting the maxillary central incisor with the microsatellite marker D18S64 (tightly linked to TNFRSF11A). This indicates that the TNFRSF11A locus, or another tightly linked gene, is associated with EARR...
- Phenytoin embryopathy: effect of epoxide hydrolase inhibitor on phenytoin exposure in utero in C57BL/6J miceJ K Hartsfield
Department of Oral Facial Development, Indiana University, Indianapolis 46202 5186, USA
Biochem Mol Med 56:131-43. 1995..This suggests either that differences in the genotypes of Swiss and C57BL/6J mice may be a contributing factor or that other teratogenic mechanisms were involved...
- Comparison of reliability in anatomical landmark identification using two-dimensional digital cephalometrics and three-dimensional cone beam computed tomography in vivoP C Chien
Department of Orthodontics and Oral Facial Genetics, Indiana University Shool of Dentistry, Indianapolis, IN, USA
Dentomaxillofac Radiol 38:262-73. 2009..To compare reliability for landmark identification on patient images from three-dimensional (3D) cone beam CT (CBCT) and digital two-dimensional (2D) lateral cephalograms...
- A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetranceE T Everett
Department of Oral Facial Development, Indiana University School of Dentistry, Indianapolis 46202, USA
Cleft Palate Craniofac J 36:533-41. 1999..To determine whether specific mutations within the fibroblast growth factor receptor 2 (FGFR2) gene that are associated with Crouzon syndrome can be present in an individual who had been assumed to be "clinically normal."..
- Dentin dysplasia, type II linkage to chromosome 4qJ A Dean
Department of Oral Facial Development, Indiana University School of Dentistry, Indianapolis 46202 5186, USA
J Craniofac Genet Dev Biol 17:172-7. 1997..1 cM, includes SPPI, D4S2691, D4S2690, D4S451, and D4S2456, and overlaps the most likely location of the DGII locus. A candidate gene for DGII should also be considered a candidate gene for dentin dysplasia, type II...
- The use of small titanium screws for orthodontic anchorageT Deguchi
Department of Orthodontics, Okayama University Graduate School of Medicine and Dentistry, 2 5 1, Shikata cho, Japan
J Dent Res 82:377-81. 2003..Analysis of these data indicates that small titanium screws were able to function as rigid osseous anchorage against orthodontic load for 3 months with a minimal (under 3 weeks) healing period...
- Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpointO T Mueller
Department of Pediatrics, University of South Florida College of Medicine, Tampa 33612
Am J Hum Genet 49:804-10. 1991..The translocation chromosome originated from an unaffected male without a visible translocation, indicating that the most likely cause of OCRL in this patient is the de novo translocation that disrupted the OCRL locus...