These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 8762878)

  • 41. Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.
    Yamamoto K; Yoshihashi H; Furuya N; Adachi M; Ito S; Tanaka Y; Masuno M; Chiyo H; Kurosawa K
    Congenit Anom (Kyoto); 2009 Mar; 49(1):8-14. PubMed ID: 19243411
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Nevoid basal cell carcinoma syndrome: review of 118 affected individuals.
    Shanley S; Ratcliffe J; Hockey A; Haan E; Oley C; Ravine D; Martin N; Wicking C; Chenevix-Trench G
    Am J Med Genet; 1994 Apr; 50(3):282-90. PubMed ID: 8042673
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Nucleolar organiser regions in odontogenic cysts and ameloblastomas.
    Allison RT; Spencer S
    Br J Biomed Sci; 1993 Dec; 50(4):309-12. PubMed ID: 8130691
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A high-resolution radiation hybrid map of the region surrounding the Gorlin syndrome gene.
    Obermayr F; Walter MA; Jones HB; Goodfellow PN; Frischauf AM
    Eur J Hum Genet; 1996; 4(4):242-5. PubMed ID: 8875192
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Nevoid basal cell carcinoma syndrome: a review of the literature and a report of a case.
    Bakaeen G; Rajab LD; Sawair FA; Hamdan MA; Dallal ND
    Int J Paediatr Dent; 2004 Jul; 14(4):279-87. PubMed ID: 15242385
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Resolution of odontogenic keratocysts of the jaw in basal cell nevus syndrome with GDC-0449.
    Goldberg LH; Landau JM; Moody MN; Kazakevich N; Holzer AM; Myers A
    Arch Dermatol; 2011 Jul; 147(7):839-41. PubMed ID: 21422324
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Loss of heterozygosity of MIR15A/MIR16-1, negative regulators of the antiapoptotic gene BCL2, is not common in odontogenic keratocysts.
    Asevedo Campos de Resende T; de Fátima Bernardes V; Carolina da Silva J; De Marco LA; Santiago Gomez R; Cavalieri Gomes C; Gonçalves Diniz M
    Oral Surg Oral Med Oral Pathol Oral Radiol; 2018 Apr; 125(4):313-316. PubMed ID: 29472118
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinical, radiographic, pathological and inherited characteristics of odontogenic keratocyst in nevoid basal cell carcinoma syndrome: a study in three Chilean families.
    Castillo-Tobar A; Urzúa B; Tirreau V; Donoso F; Pinares J; Cosmelli-Maturana R; Ortega-Pinto A
    Oral Radiol; 2023 Jul; 39(3):518-527. PubMed ID: 36436193
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.
    Olivieri C; Maraschio P; Caselli D; Martini C; Beluffi G; Maserati E; Danesino C
    Eur J Pediatr; 2003 Feb; 162(2):100-3. PubMed ID: 12548386
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Immunohistochemical analysis of the biological potential of odontogenic keratocysts.
    Kolár Z; Geierová M; Bouchal J; Pazdera J; Zboril V; Tvrdý P
    J Oral Pathol Med; 2006 Feb; 35(2):75-80. PubMed ID: 16430736
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3.
    Farndon PA; Morris DJ; Hardy C; McConville CM; Weissenbach J; Kilpatrick MW; Reis A
    Genomics; 1994 Sep; 23(2):486-9. PubMed ID: 7835901
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The odontogenic keratocyst: a benign cystic tumor?
    Ahlfors E; Larsson A; Sjögren S
    J Oral Maxillofac Surg; 1984 Jan; 42(1):10-9. PubMed ID: 6199488
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Detection of PTCH gene mutations in odontogenic keratocysts by SSCP and DNA sequencing].
    Gu XM; Li TJ
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2006 Aug; 24(4):293-6. PubMed ID: 16999341
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Nevoid basal cell carcinoma syndrome in a black child.
    Hall J; Johnston KA; McPhillips JP; Barnes SD; Elston DM
    J Am Acad Dermatol; 1998 Feb; 38(2 Pt 2):363-5. PubMed ID: 9486718
    [TBL] [Abstract][Full Text] [Related]  

  • 56. MMP-13 expression in keratocyst odontogenic tumour associated with NBCCS and sporadic keratocysts.
    Leonardi R; Matthews JB; Caltabiano R; Greco M; Lombardo C; Loreto C; Santarelli A; Lo Muzio L
    Oral Dis; 2010 Nov; 16(8):795-800. PubMed ID: 20561220
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Basal cell carcinoma syndrome: report of 10 cases.
    Sun DX; Yu Q; Wang PZ; Qian GQ
    Dentomaxillofac Radiol; 1990 Nov; 19(4):181-4. PubMed ID: 2097230
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.
    Shimkets R; Gailani MR; Siu VM; Yang-Feng T; Pressman CL; Levanat S; Goldstein A; Dean M; Bale AE
    Am J Hum Genet; 1996 Aug; 59(2):417-22. PubMed ID: 8755929
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Multiple non-syndromic odontogenic keratocysts in three siblings.
    Nirwan A; Wanjari SP; Saikhedkar R; Karun V
    BMJ Case Rep; 2013 Mar; 2013():. PubMed ID: 23505078
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Evidence of loss of heterozygosity of the PTCH gene in orthokeratinized odontogenic cyst.
    Diniz MG; Galvão CF; Macedo PS; Gomes CC; Gomez RS
    J Oral Pathol Med; 2011 Mar; 40(3):277-80. PubMed ID: 21138481
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.