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Journal Abstract Search

306 related items for PubMed ID: 31982676

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  • 2. Immunohistochemical evaluation of Sonic Hedgehog signaling pathway proteins (Shh, Ptch1, Ptch2, Smo, Gli1, Gli2, and Gli3) in sporadic and syndromic odontogenic keratocysts.
    Hoyos Cadavid AM, Kaminagakura E, Rodrigues MFSD, Pinto CAL, Teshima THN, Alves FA.
    Clin Oral Investig; 2019 Jan; 23(1):153-159. PubMed ID: 29564556
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  • 3. The immunoprofile of odontogenic keratocyst (keratocystic odontogenic tumor) that includes expression of PTCH, SMO, GLI-1 and bcl-2 is similar to ameloblastoma but different from odontogenic cysts.
    Vered M, Peleg O, Taicher S, Buchner A.
    J Oral Pathol Med; 2009 Aug; 38(7):597-604. PubMed ID: 19473442
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  • 4. Expression of the Sonic Hedgehog receptor "PATCHED" in basal cell carcinomas and odontogenic keratocysts.
    Zedan W, Robinson PA, Markham AF, High AS.
    J Pathol; 2001 Aug; 194(4):473-7. PubMed ID: 11523056
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  • 5. Dental Screening Including Panoramic Radiograph for Gorlin-Goltz Syndrome in Patients With Multiple Basal Cell Carcinomas.
    Pitak-Arnnop P, Witohendro LK, Tangmanee C, Bhakdinaronk A, Subbalekha K, Auychai P, Sirintawat N, Meningaud JP, Neff A.
    J Cutan Med Surg; 2022 Aug; 26(6):586-592. PubMed ID: 36205130
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  • 6. PTCH1 mutations in odontogenic keratocysts: are they related to epithelial cell proliferation?
    Pan S, Li TJ.
    Oral Oncol; 2009 Oct; 45(10):861-5. PubMed ID: 19362041
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  • 12. PTCH1 alterations are frequent but other genetic alterations are rare in sporadic odontogenic keratocysts.
    Qu J, Zhang J, Zhang H, Li X, Hong Y, Zhai J, Wang Y, Chen F, Li T.
    Oral Dis; 2019 Sep; 25(6):1600-1607. PubMed ID: 31162759
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  • 14. [PTCH gene mutations in odontogenic keratocysts].
    Yuan JW, Li TJ, Zhong HH, Zhao HS.
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2006 Jan; 41(1):41-4. PubMed ID: 16620627
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  • 15. PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts.
    Gu XM, Zhao HS, Sun LS, Li TJ.
    J Dent Res; 2006 Sep; 85(9):859-63. PubMed ID: 16931872
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  • 18. Delayed Diagnosis of Gorlin-Goltz Syndrome: The Importance of the Multidisciplinary Approach.
    Figueira JA, Batista FRS, Rosso K, Veltrini VC, Pavan AJ.
    J Craniofac Surg; 2018 Sep; 29(6):e530-e531. PubMed ID: 29521748
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  • 19. Basal cell carcinoma arising in association with a maxillary keratocyst in a patient with Gorlin-Goltz syndrome. Report of a case.
    Lazaridou MN, Dimitrakopoulos I, Tilaveridis I, Iliopoulos C, Heva A.
    Oral Maxillofac Surg; 2012 Mar; 16(1):127-31. PubMed ID: 21744042
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  • 20. Basal Cell Nevus (Gorlin) Syndrome with a Novel Heterozygous Deletion Frameshift Mutation (C.959delc, P.val322 Phe Fsx2) in the Ptch1 Gene Associated with Epiretinal Membrane, Odontogenic Keratocysts and without Skin Lesions and Falx Cerebri Calcification.
    Akaltun A, Eroz R, Dogan M, Bolu S, Onder HI, Onbas O, Kocabay K.
    Genet Couns; 2016 Mar; 27(2):259-62. PubMed ID: 29485834
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