-
1
-
-
0031898686
-
UVB induces atypical melanocytic lesions and melanoma in human skin
-
Atillasoy ES, Seykora JT, Soballe PW, Elenitsas R, Nesbit M, Elder DE, et al.: UVB induces atypical melanocytic lesions and melanoma in human skin. Am J Pathol 1998, 152:1179-1186.
-
(1998)
Am J Pathol
, vol.152
, pp. 1179-1186
-
-
Atillasoy, E.S.1
Seykora, J.T.2
Soballe, P.W.3
Elenitsas, R.4
Nesbit, M.5
Elder, D.E.6
-
2
-
-
0030838767
-
The molecular basis of nonmelanoma skin cancer: New understanding
-
Grossman D, Leffell DJ: The molecular basis of nonmelanoma skin cancer: new understanding [review]. Arch Dermatol 1997, 133:1263-1270. This paper is an excellent review of the current status of molecular and genetic processes in non-melanoma skin cancer.
-
(1997)
Arch Dermatol
, vol.133
, pp. 1263-1270
-
-
Grossman, D.1
Leffell, D.J.2
-
3
-
-
0023222358
-
Nevoid basal-cell carcinoma syndrome
-
Gorlin RJ: Nevoid basal-cell carcinoma syndrome [review]. Medicine 1987, 66:98-113.
-
(1987)
Medicine
, vol.66
, pp. 98-113
-
-
Gorlin, R.J.1
-
4
-
-
0026627965
-
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, et al.: Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell 1992, 69:111-117.
-
(1992)
Cell
, vol.69
, pp. 111-117
-
-
Gailani, M.R.1
Bale, S.J.2
Leffell, D.J.3
DiGiovanna, J.J.4
Peck, G.L.5
Poliak, S.6
-
5
-
-
15844386165
-
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, et al.: Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 1996, 85:841-851.
-
(1996)
Cell
, vol.85
, pp. 841-851
-
-
Hahn, H.1
Wicking, C.2
Zaphiropoulous, P.G.3
Gailani, M.R.4
Shanley, S.5
Chidambaram, A.6
-
6
-
-
15844381336
-
Human homolog of patched, a candidate gene for the basal cell nevus syndrome
-
Johnson RL, Rothman AL, Xie J, Goodrich LV, Bare JW, Bonifas JM, et al.: Human homolog of patched, a candidate gene for the basal cell nevus syndrome. Science 1996, 272:1668-1671.
-
(1996)
Science
, vol.272
, pp. 1668-1671
-
-
Johnson, R.L.1
Rothman, A.L.2
Xie, J.3
Goodrich, L.V.4
Bare, J.W.5
Bonifas, J.M.6
-
7
-
-
0030876833
-
Developmental genes and cancer: Role of patched in basal cell carcinoma of the skin
-
Gailani MR, Bale AE: Developmental genes and cancer: role of patched in basal cell carcinoma of the skin [review]. J Natl Cancer Inst 1997, 89:1103-1109. An excellent review on the patched gene in basal cell carcinomas is presented in this paper.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1103-1109
-
-
Gailani, M.R.1
Bale, A.E.2
-
8
-
-
0027760995
-
Sonic hedgehog mediates the polarizing activity of the ZPA
-
Riddle RD, Johnson RL, Laufer E, Tabin C: Sonic hedgehog mediates the polarizing activity of the ZPA. Cell 1993, 75:1401-1416.
-
(1993)
Cell
, vol.75
, pp. 1401-1416
-
-
Riddle, R.D.1
Johnson, R.L.2
Laufer, E.3
Tabin, C.4
-
9
-
-
0029004233
-
Floor plate and motor neuron induction by different concentrations of the amino-terminal cleavage product of sonic hedgehog autoproteolysis
-
Roelink H, Porter JA, Chiang C, Tanabe Y, Chang DT, Beachy PA, Jessell TM: Floor plate and motor neuron induction by different concentrations of the amino-terminal cleavage product of sonic hedgehog autoproteolysis. Cell 1995, 81:445-455.
-
(1995)
Cell
, vol.81
, pp. 445-455
-
-
Roelink, H.1
Porter, J.A.2
Chiang, C.3
Tanabe, Y.4
Chang, D.T.5
Beachy, P.A.6
Jessell, T.M.7
-
10
-
-
0030844141
-
Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours
-
Dahmane N, Lee J, Robins P, Heller P, Ruiz I, Altaba A: Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours. Nature 1997, 389:876-881.
-
(1997)
Nature
, vol.389
, pp. 876-881
-
-
Dahmane, N.1
Lee, J.2
Robins, P.3
Heller, P.4
Ruiz, I.5
Altaba, A.6
-
11
-
-
0031913524
-
Activating smoothened mutations in sporadic basal-cell carcinoma
-
Xie J, Murone M, Luoh SM, Ryan A, Gu Q, Zhang C, et al.: Activating Smoothened mutations in sporadic basal-cell carcinoma. Nature 1998, 391:90-92.
-
(1998)
Nature
, vol.391
, pp. 90-92
-
-
Xie, J.1
Murone, M.2
Luoh, S.M.3
Ryan, A.4
Gu, Q.5
Zhang, C.6
-
12
-
-
0030955557
-
Basal cell carcinomas in mice overexpressing sonic hedgehog
-
Oro AE, Higgins KM, Hu Z, Bonifas JM, Epstein EH Jr, Scott MP: Basal cell carcinomas in mice overexpressing sonic hedgehog. Science 1997, 276:817-821.
-
(1997)
Science
, vol.276
, pp. 817-821
-
-
Oro, A.E.1
Higgins, K.M.2
Hu, Z.3
Bonifas, J.M.4
Epstein E.H., Jr.5
Scott, M.P.6
-
13
-
-
0030802458
-
Induction of basal cell carcinoma features in transgenic human skin expressing Sonic Hedgehog
-
Fan H, Oro AE, Scott MP, Khavari PA: Induction of basal cell carcinoma features in transgenic human skin expressing Sonic Hedgehog. Nat Med 1997, 3:788-792.
-
(1997)
Nat Med
, vol.3
, pp. 788-792
-
-
Fan, H.1
Oro, A.E.2
Scott, M.P.3
Khavari, P.A.4
-
14
-
-
0031837549
-
Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome
-
Aszterbaum M, Rothman A, Johnson RL, Fisher M, Xie J, Bonifas JM, et al.: Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome. J Invest Dermatol 1998, 110:885-888.
-
(1998)
J Invest Dermatol
, vol.110
, pp. 885-888
-
-
Aszterbaum, M.1
Rothman, A.2
Johnson, R.L.3
Fisher, M.4
Xie, J.5
Bonifas, J.M.6
-
15
-
-
0017970363
-
Origin of familial malignant melanomas from heritable melanocytic lesions. The B-K syndrome
-
Clark WH Jr, Reimer RR, Greene M, Ainsworth AM, Mastrangelo MJ: Origin of familial malignant melanomas from heritable melanocytic lesions. The B-K syndrome. Arch Dermatol 1978, 114:732-738.
-
(1978)
Arch Dermatol
, vol.114
, pp. 732-738
-
-
Clark W.H., Jr.1
Reimer, R.R.2
Greene, M.3
Ainsworth, A.M.4
Mastrangelo, M.J.5
-
16
-
-
0018123909
-
Familial atypical multiple molemelanoma syndrome
-
Lynch HT, Frichot BC III, Lynch JF: Familial atypical multiple molemelanoma syndrome. J Med Genet 1978, 15:352-356.
-
(1978)
J Med Genet
, vol.15
, pp. 352-356
-
-
Lynch, H.T.1
Frichot B.C. III2
Lynch, J.F.3
-
17
-
-
0021940118
-
High risk of malignant melanoma in melanoma-prone families with dysplastic nevi
-
Greene MH, Clark WH Jr, Tucker MA, Kraemer KH, Elder DE, Fraser MC: High risk of malignant melanoma in melanoma-prone families with dysplastic nevi. Ann Intern Med 1985, 102:458-465.
-
(1985)
Ann Intern Med
, vol.102
, pp. 458-465
-
-
Greene, M.H.1
Clark W.H., Jr.2
Tucker, M.A.3
Kraemer, K.H.4
Elder, D.E.5
Fraser, M.C.6
-
18
-
-
0030912777
-
Clinically recognized dysplastic nevi. A central risk factor for cutaneous melanoma
-
Tucker MA, Halpern A, Holly EA, Hartge P, Elder DE, Sagebiel RW, et al.: Clinically recognized dysplastic nevi. A central risk factor for cutaneous melanoma. JAMA 1997, 277:1439-1444.
-
(1997)
JAMA
, vol.277
, pp. 1439-1444
-
-
Tucker, M.A.1
Halpern, A.2
Holly, E.A.3
Hartge, P.4
Elder, D.E.5
Sagebiel, R.W.6
-
19
-
-
0024320151
-
Mapping the gene for hereditary cutaneous malignant melanomadysplastic nevus to chromosome 1p
-
Published erratum appears in N Engl J Med 1991,324:925
-
Bale SJ, Dracopoli NC, Tucker MA, Clark WH Jr, Fraser MC, Stanger BZ, et al.: Mapping the gene for hereditary cutaneous malignant melanomadysplastic nevus to chromosome 1p N Engl J Med 1989, 320:1367-1372. [Published erratum appears in N Engl J Med 1991,324:925.]
-
(1989)
N Engl J Med
, vol.320
, pp. 1367-1372
-
-
Bale, S.J.1
Dracopoli, N.C.2
Tucker, M.A.3
Clark W.H., Jr.4
Fraser, M.C.5
Stanger, B.Z.6
-
20
-
-
0028013327
-
Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity
-
Goldstein AM, Dracopoli NC, Engelstein M, Fraser MC, Clark WH Jr, Tucker MA: Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity. Am J Hum Genet 1994, 54:489-496.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 489-496
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Engelstein, M.3
Fraser, M.C.4
Clark W.H., Jr.5
Tucker, M.A.6
-
21
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain JW, et al.: Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science 1992, 258:1148-1152.
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
Lewis, C.M.4
Anderson, D.E.5
Fountain, J.W.6
-
22
-
-
0027495164
-
Linkage analysis in Dutch familial atypical multiple molemelanoma (FAMMM) syndrome families. Effect of naevus count
-
Gruis NA, Sandkuijl LA, Weber JL, Van der Zee A, Borgstein AM, Bergman, W, Frants RR: Linkage analysis in Dutch familial atypical multiple molemelanoma (FAMMM) syndrome families. Effect of naevus count. Melanoma Res 1993, 3:271-277.
-
(1993)
Melanoma Res
, vol.3
, pp. 271-277
-
-
Gruis, N.A.1
Sandkuijl, L.A.2
Weber, J.L.3
Van Der Zee, A.4
Borgstein, A.M.5
Bergman, W.6
Frants, R.R.7
-
23
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis NA, Weaver-Feldhaus J, Liu Q, Harshman K, Tavtigian SV, et al.: A cell cycle regulator potentially involved in genesis of many tumor types. Science 1994, 264:436-440.
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
Liu, Q.4
Harshman, K.5
Tavtigian, S.V.6
-
24
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori T, Miura K, Wu DJ, Lois A, Takabayashi K, Carson DA: Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature 1994, 368:753-756.
-
(1994)
Nature
, vol.368
, pp. 753-756
-
-
Nobori, T.1
Miura, K.2
Wu, D.J.3
Lois, A.4
Takabayashi, K.5
Carson, D.A.6
-
25
-
-
0029587551
-
Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest
-
Quelle DE, Zindy F, Ashmun RA, Sherr CJ: Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell 1995, 83:993-1000.
-
(1995)
Cell
, vol.83
, pp. 993-1000
-
-
Quelle, D.E.1
Zindy, F.2
Ashmun, R.A.3
Sherr, C.J.4
-
26
-
-
0028982932
-
A novel p16INK4A transcript
-
Mao L, Merlo A, Bedi G, Shapiro GI, Edwards CD, Rollins BJ, Sidransky D: A novel p16INK4A transcript. Cancer Res 1995, 55:2995-2997.
-
(1995)
Cancer Res
, vol.55
, pp. 2995-2997
-
-
Mao, L.1
Merlo, A.2
Bedi, G.3
Shapiro, G.I.4
Edwards, C.D.5
Rollins, B.J.6
Sidransky, D.7
-
27
-
-
0029060657
-
Complex structure and regulation of the P16 (MTS1) locus
-
Stone S, Jiang P, Dayananth P, Tavtigian SV, Katcher H, Parry D, et al.: Complex structure and regulation of the P16 (MTS1) locus. Cancer Res 1995, 55:2988-2994.
-
(1995)
Cancer Res
, vol.55
, pp. 2988-2994
-
-
Stone, S.1
Jiang, P.2
Dayananth, P.3
Tavtigian, S.V.4
Katcher, H.5
Parry, D.6
-
28
-
-
0029993450
-
Role of the INK4a locus in tumor suppression and cell mortality
-
Serrano M, Lee H, Chin L, Cordon-Cardo C, Beach D, Depinho RA: Role of the INK4a locus in tumor suppression and cell mortality. Cell 1996, 85:27-37.
-
(1996)
Cell
, vol.85
, pp. 27-37
-
-
Serrano, M.1
Lee, H.2
Chin, L.3
Cordon-Cardo, C.4
Beach, D.5
Depinho, R.A.6
-
29
-
-
0027769876
-
A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4
-
Serrano M, Hannon GJ, Beach D: A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature 1993, 366:704-707.
-
(1993)
Nature
, vol.366
, pp. 704-707
-
-
Serrano, M.1
Hannon, G.J.2
Beach, D.3
-
30
-
-
0031894534
-
Molecular genetics of familial cutaneous melanoma
-
Haluska FG, Hodi FS: Molecular genetics of familial cutaneous melanoma [review]. J Clin Oncol 1998, 16:670-682. This is an excellent review emphasizing the importance of the role of the p16 gene in melanoma.
-
(1998)
J Clin Oncol
, vol.16
, pp. 670-682
-
-
Haluska, F.G.1
Hodi, F.S.2
-
31
-
-
0029664339
-
Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
-
Zuo L, Weger J, Yang Q, Goldstein AM, Tucker MA, Walker GJ, et al.: Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma. Nat Genet 1996, 12:97-99.
-
(1996)
Nat Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
Goldstein, A.M.4
Tucker, M.A.5
Walker, G.J.6
-
32
-
-
6844226190
-
Prevalence of pl 6 and CDK4 germline mutations in 48 melanoma-prone families in France
-
The French Familial Melanoma Study Group. [Published erratum appears in Hum Mol Genet 1998 7:941]
-
Soufir N, Avril MF, Chompret A, Demenais F, Bombled J, Spatz A, et al.: Prevalence of pl 6 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. Hum Mol Genet 1998, 7:209-216. [Published erratum appears in Hum Mol Genet 1998 7:941].
-
(1998)
Hum Mol Genet
, vol.7
, pp. 209-216
-
-
Soufir, N.1
Avril, M.F.2
Chompret, A.3
Demenais, F.4
Bombled, J.5
Spatz, A.6
-
33
-
-
0031808138
-
Expression of the tumor suppressor gene product p16INK4 in benign and malignant melanocytic lesions
-
Keller-Melchior R, Schmidt R, Piepkorn M: Expression of the tumor suppressor gene product p16INK4 in benign and malignant melanocytic lesions. J Invest Dermatol 1998, 110:932-938.
-
(1998)
J Invest Dermatol
, vol.110
, pp. 932-938
-
-
Keller-Melchior, R.1
Schmidt, R.2
Piepkorn, M.3
-
34
-
-
0030610586
-
Loss of expression of the p16INK4/CDKN2 gene in cutaneous malignant melanoma correlates with tumor cell proliferation and invasive stage
-
Talve L, Sauroja I, Collan Y, Punnonen K, Ekfors T: Loss of expression of the p16INK4/CDKN2 gene in cutaneous malignant melanoma correlates with tumor cell proliferation and invasive stage. Int J Cancer 1997, 74:255-259.
-
(1997)
Int J Cancer
, vol.74
, pp. 255-259
-
-
Talve, L.1
Sauroja, I.2
Collan, Y.3
Punnonen, K.4
Ekfors, T.5
-
35
-
-
0023835460
-
Thymine dimer repair in fibroblasts of patients with dysplastic naevus syndrome (DNS)
-
Roth M, Boyle JM, Muller H: Thymine dimer repair in fibroblasts of patients with dysplastic naevus syndrome (DNS). Experientia 1988, 44:169-171.
-
(1988)
Experientia
, vol.44
, pp. 169-171
-
-
Roth, M.1
Boyle, J.M.2
Muller, H.3
-
36
-
-
10544224961
-
Enzyme therapy of xeroderma pigmentosum: Safety and efficacy testing of T4N5 liposome lotion containing a prokaryotic DNA repair enzyme
-
Yarosh D, Klein J, Kibitel J, Alas L, O'Connor A, Cummings B, et al.: Enzyme therapy of xeroderma pigmentosum: safety and efficacy testing of T4N5 liposome lotion containing a prokaryotic DNA repair enzyme. Photodermatol Photoimmunol Photomed 1996, 12:122-130.
-
(1996)
Photodermatol Photoimmunol Photomed
, vol.12
, pp. 122-130
-
-
Yarosh, D.1
Klein, J.2
Kibitel, J.3
Alas, L.4
O'Connor, A.5
Cummings, B.6
-
37
-
-
0028053988
-
Xeroderma pigmentosum and related disorders: Examining the linkage between defective DNA repair and cancer
-
Kraemer KH, Levy DD, Parris CN, Gozukara EM, Moriwaki S, Adelberg S, Seidman MM: Xeroderma pigmentosum and related disorders: examining the linkage between defective DNA repair and cancer [review]. J Invest Dermatol 1994, 103:96S-101S.
-
(1994)
J Invest Dermatol
, vol.103
-
-
Kraemer, K.H.1
Levy, D.D.2
Parris, C.N.3
Gozukara, E.M.4
Moriwaki, S.5
Adelberg, S.6
Seidman, M.M.7
-
38
-
-
0014421995
-
Defective repair replication of DNA in xeroderma pigmentosum
-
Cleaver JE: Defective repair replication of DNA in xeroderma pigmentosum. Nature 1968, 218:652-656.
-
(1968)
Nature
, vol.218
, pp. 652-656
-
-
Cleaver, J.E.1
-
39
-
-
0030855328
-
The molecular basis of xeroderma pigmentosum
-
Copeland NE, Hanke CW, Michalak JA: The molecular basis of xeroderma pigmentosum [review]. Dermatol Surg 1997, 23:447-455. This article is a good review of the molecular processes involved in XP.
-
(1997)
Dermatol Surg
, vol.23
, pp. 447-455
-
-
Copeland, N.E.1
Hanke, C.W.2
Michalak, J.A.3
-
41
-
-
0032101146
-
Defective bypass replication of a leading strand cyclobutane thymine dimer in xeroderma pigmentosum variant cell extracts
-
Svoboda DL, Briley LP, Vos JM: Defective bypass replication of a leading strand cyclobutane thymine dimer in xeroderma pigmentosum variant cell extracts. Cancer Res 1998, 58:2445-2448.
-
(1998)
Cancer Res
, vol.58
, pp. 2445-2448
-
-
Svoboda, D.L.1
Briley, L.P.2
Vos, J.M.3
-
42
-
-
0030925436
-
Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis
-
Cordeiro-Stone M, Zaritskaya LS, Price LK, Kaufmann WK: Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis. J Biol Chem 1997, 272:13945-13954.
-
(1997)
J Biol Chem
, vol.272
, pp. 13945-13954
-
-
Cordeiro-Stone, M.1
Zaritskaya, L.S.2
Price, L.K.3
Kaufmann, W.K.4
-
43
-
-
0023130695
-
Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases
-
Kraemer KH, Lee MM, Scotto J: Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases. Arch Dermatol 1987, 123:241-250.
-
(1987)
Arch Dermatol
, vol.123
, pp. 241-250
-
-
Kraemer, K.H.1
Lee, M.M.2
Scotto, J.3
-
44
-
-
7144254441
-
Melanocortin 1 receptor variants in an Irish population
-
Smith R, Healy E, Siddiqui S, Flanagan N, Steijlen PM, Rosdahl I, et al.: Melanocortin 1 receptor variants in an Irish population. J Invest Dermatol 1998, 111:119-122.
-
(1998)
J Invest Dermatol
, vol.111
, pp. 119-122
-
-
Smith, R.1
Healy, E.2
Siddiqui, S.3
Flanagan, N.4
Steijlen, P.M.5
Rosdahl, I.6
-
45
-
-
0029793064
-
Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients
-
Chidambaram A, Goldstein AM, Gailani MR, Gerrard B, Bale SJ, DiGiovanna JJ, et al.: Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients. Cancer Res 1996, 56:4599-4601.
-
(1996)
Cancer Res
, vol.56
, pp. 4599-4601
-
-
Chidambaram, A.1
Goldstein, A.M.2
Gailani, M.R.3
Gerrard, B.4
Bale, S.J.5
DiGiovanna, J.J.6
-
46
-
-
0029841366
-
Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: Different in vivo mechanisms of PTCH inactivation
-
Unden AB, Holmberg E, Lundh-Rozell B, Stahle-Backdahl M, Zaphiropoulos, PG, Toftgard R, Vorechovsky I: Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation. Cancer Res 1996, 56:4562-4565.
-
(1996)
Cancer Res
, vol.56
, pp. 4562-4565
-
-
Unden, A.B.1
Holmberg, E.2
Lundh-Rozell, B.3
Stahle-Backdahl, M.4
Zaphiropoulos, P.G.5
Toftgard, R.6
Vorechovsky, I.7
-
47
-
-
16044363842
-
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
-
Gailani MR, Stahle-Backdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, et al.: The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nat Genet 1996, 14:78-81.
-
(1996)
Nat Genet
, vol.14
, pp. 78-81
-
-
Gailani, M.R.1
Stahle-Backdahl, M.2
Leffell, D.J.3
Glynn, M.4
Zaphiropoulos, P.G.5
Pressman, C.6
-
48
-
-
12844276949
-
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident
-
Wicking C, Shanley S, Smyth I, Gillies S, Negus K, Graham S, et al.: Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. Am J Hum Genet 1997, 60:21-26.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 21-26
-
-
Wicking, C.1
Shanley, S.2
Smyth, I.3
Gillies, S.4
Negus, K.5
Graham, S.6
-
49
-
-
0011102935
-
The tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog
-
Stone DM, Hynes M, Armanini M, Swanson TA, Gu Q Johnson RL, et al.: The tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog. Nature 1996, 384:129-134.
-
(1996)
Nature
, vol.384
, pp. 129-134
-
-
Stone, D.M.1
Hynes, M.2
Armanini, M.3
Swanson, T.A.4
Gu, Q.5
Johnson, R.L.6
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