Research & Literature

Formate assay in body fluids: application in methanol poisoning.

Makar AB, McMartin KE, Palese M, Tephly TR

Biochemical medicine 1975; (13(2)):117-26 doi:10.1016/0006-2944(75)90147-7.

Delineation of the intimate details of the backbone conformation of pyridine nucleotide coenzymes in aqueous solution.

Bose KS, Sarma RH

Biochemical and biophysical research communications 1975; (66(4)):1173-9 doi:10.1016/0006-291x(75)90482-9.

Metal substitutions incarbonic anhydrase: a halide ion probe study.

Smith RJ, Bryant RG

Biochemical and biophysical research communications 1975; (66(4)):1281-6 doi:10.1016/0006-291x(75)90498-2.

Effect of chloroquine on cultured fibroblasts: release of lysosomal hydrolases and inhibition of their uptake.

Wiesmann UN, DiDonato S, Herschkowitz NN

Biochemical and biophysical research communications 1975; (66(4)):1338-43 doi:10.1016/0006-291x(75)90506-9.

Histological and Ultrastructure Analysis of Dentin Dysplasia Type I in Primary Teeth: A Case Report.

Pintor A, Alexandria A, Marques A, et al.

Ultrastructural pathology 2015; (39(4)):281-5 doi:10.3109/01913123.2014.1002960.

Dentin dysplasia type I - A rare entity.

Malik S, Gupta S, Wadhwan V, Suhasini GP

Journal of oral and maxillofacial pathology : JOMFP 2015; (19(1)):110 doi:10.4103/0973-029X.157220.

Dentin dysplasia type I-novel findings in deciduous and permanent teeth.

Ye X, Li K, Liu L, et al.

BMC oral health 2015; (15()):163 doi:10.1186/s12903-015-0149-9.

Dentin Dysplasia in Notum Knockout Mice.

Vogel P, Read RW, Hansen GM, et al.

Veterinary pathology 2016; (53(4)):853-62 doi:10.1177/0300985815626778.

A splicing mutation in VPS4B causes dentin dysplasia I.

Yang Q, Chen D, Xiong F, et al.

Journal of medical genetics 2016; (53(9)):624-33 doi:10.1136/jmedgenet-2015-103619.

Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.

Xiong F, Ji Z, Liu Y, et al.

Human mutation 2017; (38(1)):95-104 doi:10.1002/humu.23130.

Secondary Alveolar Bone Grafting in Patients Born With Unilateral Cleft Lip and Palate: A 20-Year Follow-up.

Jabbari F, Wiklander L, Reiser E, et al.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2018; (55(2)):173-179 doi:10.1177/1055665617726999.

Dentin dysplasia type I-A dental disease with genetic heterogeneity.

Chen D, Li X, Lu F, et al.

Oral diseases 2019; (25(2)):439-446 doi:10.1111/odi.12861.

Dentin dysplasia: diagnostic challenges.

Alhilou A, Beddis HP, Mighell AJ, Durey K

BMJ case reports 2018; (2018()) doi:10.1136/bcr-2017-223942.

Are Hertwig's epithelial root sheath cells necessary for periodontal formation by dental follicle cells?

Guo Y, Guo W, Chen J, et al.

Archives of oral biology 2018; (94()):1-9 doi:10.1016/j.archoralbio.2018.06.014.

A rare case diagnosed as dentin dysplasia type II.

Perlea P, Dragomir C, Bodeanu A, et al.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2018; (59(1)):359-365.

Vacuolar protein sorting 4B regulates the proliferation and odontoblastic differentiation of human dental pulp stem cells through the Wnt-β-catenin signalling pathway.

Pan Y, Lu T, Peng L, et al.

Artificial cells, nanomedicine, and biotechnology 2019; (47(1)):2575-2584 doi:10.1080/21691401.2019.1629950.

Novel frameshift mutations in DSPP cause dentin dysplasia type II.

Lee JW, Hong J, Seymen F, et al.

Oral diseases 2019; (25(8)):2044-2046 doi:10.1111/odi.13182.

Dentin dysplasia Type I: A rare case report.

Akhil Jose EJ, Palathingal P, Baby D, Thachil JM

Journal of oral and maxillofacial pathology : JOMFP 2019; (23(2)):309 doi:10.4103/jomfp.JOMFP_132_19.

A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review.

Gulati N, Juneja S, Singh A, Singh I

Indian journal of dental research : official publication of Indian Society for Dental Research 2019; (30(4)):643-646 doi:10.4103/ijdr.IJDR_318_18.

Full Regeneration of Maxillary Alveolar Bone Using Autogenous Partially Demineralized Dentin Matrix and Particulate Cancellous Bone and Marrow for Implant-Supported Full Arch Rehabilitation.

Umebayashi M, Ohba S, Kurogi T, et al.

The Journal of oral implantology 2020; (46(2)):122-127 doi:10.1563/aaid-joi-D-19-00315.

Eleven-year follow-up of reconstruction with autogenous iliac bone graft and implant-supported fixed complete denture for severe maxillary atrophy: A case report.

Lee JH, Yeo IL

Medicine 2020; (99(9)):e18950 doi:10.1097/MD.0000000000018950.

VPS4B mutation impairs the osteogenic differentiation of dental follicle cells derived from a patient with dentin dysplasia type I.

Li Q, Lu F, Chen T, et al.

International journal of oral science 2020; (12(1)):22 doi:10.1038/s41368-020-00088-z.

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss.

Morkmued S, Clauss F, Schuhbaur B, et al.

Scientific reports 2020; (10(1)):14817 doi:10.1038/s41598-020-71749-6.

Endodontic treatment of dentin dysplasia type I D.

Buchanan GD, Tredoux S, Nel C, Gamieldien MY

Australian endodontic journal : the journal of the Australian Society of Endodontology Inc 2021; (47(2)):343-349 doi:10.1111/aej.12444.

Guided endodontic treatment of multiple teeth with dentin dysplasia: a case report.

Krug R, Volland J, Reich S, et al.

Head & face medicine 2020; (16(1)):27 doi:10.1186/s13005-020-00240-4.

An unusual variation of radicular dentin dysplasia: A rare case report with review of literature.

Patnana AK, Chugh VK, Chugh A

Indian journal of dental research : official publication of Indian Society for Dental Research 2020; (31(5)):807-812 doi:10.4103/ijdr.IJDR_372_19.

Orthodontic Treatment of a Patient with Dentin Dysplasia Type I and Bilateral Maxillary Canine Impaction: Case Presentation and a Family-Based Genetic Analysis.

Papagiannis A, Fanourakis G, Mitsea A, et al.

Children (Basel, Switzerland) 2021; (8(6)) doi:10.3390/children8060519.

Dentinogenesis imperfecta type 2: a case report.

Mohan KR, Narayanan M, Ravikumar PT

General dentistry 2021; (69(6)):74-76.

A case of multiple rootless teeth: A case report and review.

Gopalakrishnan S, Balasubramaniam N, Ramamoorthi R, Vedachalam R

Journal of oral and maxillofacial pathology : JOMFP 2021; (25(3)):559 doi:10.4103/jomfp.jomfp_337_20.

Translated Mutant DSPP mRNA Expression Level Impacts the Severity of Dentin Defects.

Kim YJ, Lee Y, Zhang H, et al.

Journal of personalized medicine 2022; (12(6)) doi:10.3390/jpm12061002.

A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.

Yuan M, Zheng X, Xue Y, et al.

Oral diseases 2023; (29(6)):2394-2400 doi:10.1111/odi.14494.

Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients.

Du Q, Cao L, Yan N, et al.

Clinical oral investigations 2023; (27(7)):3885-3894 doi:10.1007/s00784-023-05009-y.

External mandibular fixation for gunshot fractures: report of 2 cases.

Elbir B, Kolsuz N, Varol A

Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES 2023; (29(6)):741-745 doi:10.14744/tjtes.2022.77315.

Type I Dentin Dysplasia: The Literature Review and Case Report of a Family Affected by Misrecognition and Late Diagnosis.

Putrino A, Caputo M, Galeotti A, et al.

Medicina (Kaunas, Lithuania) 2023; (59(8)) doi:10.3390/medicina59081477.

Use of Individually Designed CAD/CAM Suprastructures for Dental Reconstruction in Patients with Cleft Lip and Palate.

Mäntynen P, Laurila M, Strausz T, et al.

Dentistry journal 2023; (11(9)) doi:10.3390/dj11090212.

Impaired breakdown of Herwig's epithelial root sheath disturbs tooth root development.

Jeong JK, Kim TH, Choi H, Cho ES

Developmental dynamics : an official publication of the American Association of Anatomists 2024; (253(4)):423-434 doi:10.1002/dvdy.667.

Prosthetic Oral Rehabilitation with CAD/CAM Suprastructures in Patients with Severe Tissue Deficits: A Case Series.

Laurila M, Mäntynen P, Mauno J, Suojanen J

Dentistry journal 2023; (11(12)) doi:10.3390/dj11120289.

Removal of fiber posts using conventional versus guided endodontics: a comparative study of dentin loss and complications.

Krug R, Schwarz F, Dullin C, et al.

Clinical oral investigations 2024; (28(3)):192 doi:10.1007/s00784-024-05577-7.

Reviving a Smile: A Multidisciplinary Approach to Dentin Dysplasia.

Kr AV, Raja K, Krishnan RK, et al.

Cureus 2024; (16(5)):e59697 doi:10.7759/cureus.59697.

A Novel Approach to the Management of Dentin Dysplasia Using Zygoma Implants: A Case Report.

Sharma G, Mundada B, Bhola N, et al.

Cureus 2024; (16(8)):e68099 doi:10.7759/cureus.68099.

A Novel Variant in Dentin Sialophosphoprotein (DSPP) Gene Causes Dentinogenesis Imperfecta Type III: Case Report.

Wang Y, Xu X, Ding Y, Yuan G

Molecular genetics & genomic medicine 2025; (13(3)):e70087 doi:10.1002/mgg3.70087.

Endodontic Management of Dentin Dysplasia Type II in a Pediatric Patient: A Case Report.

Saberi E, Rezvani S

Iranian endodontic journal 2025; (20(1)):e17 doi:10.22037/iej.v20i1.47021.

Beyond the diagnosis: Unraveling DSPP genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta.

Boonyakanog A, Sriwangyang K, Eamtanaporn T, et al.

The Japanese dental science review 2026; (62()):46-56 doi:10.1016/j.jdsr.2026.01.001.

[Clinical and genetic analysis of a Chinese pedigree affected with Hereditary dentin dysplasia type II due to a variant of DSPP gene].

Li F, Yang Y, Liu Y, et al.

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2025; (42(11)):1329-1336 doi:10.3760/cma.j.cn511374-20241219-00668.