BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 9059667)

  • 21. Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9.
    Gailani MR; Bale SJ; Leffell DJ; DiGiovanna JJ; Peck GL; Poliak S; Drum MA; Pastakia B; McBride OW; Kase R
    Cell; 1992 Apr; 69(1):111-7. PubMed ID: 1348213
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.
    Bonifas JM; Bare JW; Kerschmann RL; Master SP; Epstein EH
    Hum Mol Genet; 1994 Mar; 3(3):447-8. PubMed ID: 8012356
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Complications of the nevoid basal cell carcinoma syndrome: a case report.
    Walter AW; Pivnick EK; Bale AE; Kun LE
    J Pediatr Hematol Oncol; 1997; 19(3):258-62. PubMed ID: 9201152
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Location of gene for Gorlin syndrome.
    Farndon PA; Del Mastro RG; Evans DG; Kilpatrick MW
    Lancet; 1992 Mar; 339(8793):581-2. PubMed ID: 1347096
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical and genetic study in 22 patients with basal cell nevus syndrome].
    Pruvost-Balland C; Gorry P; Boutet N; Magnaldo T; Mamelle G; Margulis A; Kolb F; Duvillard P; Spatz A; Brugières L; Chompret A; Avril MF
    Ann Dermatol Venereol; 2006 Feb; 133(2):117-23. PubMed ID: 16508594
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [A nevoid basal cell carcinoma syndrome with chromosomal aberration].
    Sasaki K; Yoshimoto T; Nakao T; Minagawa K; Takahashi Y; Watanabe Y; Tanabe C
    No To Hattatsu; 2000 Jan; 32(1):49-55. PubMed ID: 10655752
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.
    Hahn H; Wicking C; Zaphiropoulous PG; Gailani MR; Shanley S; Chidambaram A; Vorechovsky I; Holmberg E; Unden AB; Gillies S; Negus K; Smyth I; Pressman C; Leffell DJ; Gerrard B; Goldstein AM; Dean M; Toftgard R; Chenevix-Trench G; Wainwright B; Bale AE
    Cell; 1996 Jun; 85(6):841-51. PubMed ID: 8681379
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two male patients with nevoid basal cell carcinoma syndrome from Turkey.
    Tümer C; Er N; Balci S; Ataç A
    Turk J Pediatr; 2001; 43(4):351-5. PubMed ID: 11765170
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The human growth-arrest-specific gene GAS1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome.
    Wicking C; Breen M; Negus K; Berkman J; Evdokiou A; Cowled P; Chenevix-Trench G; Wainwright B
    Cytogenet Cell Genet; 1995; 68(1-2):119-21. PubMed ID: 7956349
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site.
    Bare JW; Lebo RV; Epstein EH
    Cancer Res; 1992 Mar; 52(6):1494-8. PubMed ID: 1540957
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Nevoid basal-cell syndrome: literature review and case report in a family.
    José Tincani A; Santos Martins A; Gomes Andrade R; Franco Mello EJ; Camargo Bueno MA
    Sao Paulo Med J; 1995; 113(3):917-21. PubMed ID: 8728727
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region.
    Levanat S; Chidambaram A; Wicking C; Bray-Ward P; Pressman C; Toftgard R; Gailani MR; Myers JC; Wainwright B; Dean M; Bale AE
    Cytogenet Cell Genet; 1997; 76(3-4):208-13. PubMed ID: 9186526
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.
    Vorechovský I; Tingby O; Hartman M; Strömberg B; Nister M; Collins VP; Toftgård R
    Oncogene; 1997 Jul; 15(3):361-6. PubMed ID: 9233770
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.
    Panhuysen CI; Karban A; Knodle Manning A; Bayless TM; Duerr RH; Bailey-Wilson JE; Epstein EH; Brant SR
    Hum Genet; 2006 Aug; 120(1):31-41. PubMed ID: 16733713
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Nevoid basal cell carcinoma syndrome.
    Bohnert E; Jung EG
    Arch Dermatol Res; 1989; 281(3):218. PubMed ID: 2774653
    [No Abstract]   [Full Text] [Related]  

  • 38. Physical mapping of the 5 Mb D9S196-D9S180 interval harboring the basal cell nevus syndrome gene and localization of six genes in this region.
    Xie J; Quinn A; Zhang X; Bare J; Rothman A; Collins C; Cutone S; Rutter M; McCormick MK; Epstein E
    Genes Chromosomes Cancer; 1997 Apr; 18(4):305-9. PubMed ID: 9087571
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts.
    Lench NJ; High AS; Markham AF; Hume WJ; Robinson PA
    Eur J Cancer B Oral Oncol; 1996 May; 32B(3):202-6. PubMed ID: 8762878
    [TBL] [Abstract][Full Text] [Related]  

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