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Bone|May 12, 2019
A novel combination of biallelic ALPL mutations associated with adult hypophosphatasia: A phenotype-genotype association and computational analysis studyLuciane Martins, Amanda Bandeira de Almeida, Elis Janaína Lira Dos Santos, et al.Plos One|May 6, 2016
Secretome Profiling of Periodontal Ligament from Deciduous and Permanent Teeth Reveals a Distinct Expression Pattern of Laminin ChainsPriscila A Giovani, Cristiane R Salmon, Luciane Martins, et al.Journal of Molecular Graphics & Modelling|August 6, 2017
Computational analysis for GNAQ mutations: New insights on the molecular etiology of Sturge-Weber syndromeLuciane Martins, Priscila Alves Giovani, Pedro Diniz Rebouças, et al.Bone|June 25, 2013
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotypeLuciane Martins, Thaisângela L Rodrigues, Mariana Martins Ribeiro, et al.Diabetes|February 28, 2004
Mice with targeted disruption of the Dio2 gene have cold-induced overexpression of the uncoupling protein 1 gene but fail to increase brown adipose tissue lipogenesis and adaptive thermogenesisMarcelo A Christoffolete, Camila C G Linardi, Lucia de Jesus, et al.Journal of Periodontal Research|November 19, 2020
Comparative proteomic analysis of dental cementum from deciduous and permanent teethPriscila A Giovani, Luciane Martins, Cristiane R Salmon, et al.Antimicrobial Stewardship & Healthcare Epidemiology : ASHE|April 27, 2026
Antimicrobial resistance before and after the COVID-19 pandemic in Northern BrazilJosé Eudes de Carvalho Neri, Julius Caesar Mendes Soares Monteiro, Lorena Luciane Martins Rodrigues, et al.Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|October 15, 2018
Variable expressivity and novel PTEN mutations in Cowden syndromeRenato Assis Machado, Lívia Maris Ribeiro Paranaíba, Luciane Martins, et al.Journal of Periodontology|August 3, 2019
Novel rare frameshift variation in aggressive periodontitis: Exomic and familial-screening analysisTiago Taiete, Marcio Z Casati, Luciane Martins, et al.International Journal of Molecular Sciences|January 8, 2023
Childhood Hypophosphatasia Associated with a Novel Biallelic ALPL Variant at the TNSALP Dimer InterfaceLuciane Martins, Luis Gustavo F Lessa, Taccyanna M Ali, et al.Pageof 2