J. Fountain

发表

Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds

P. Pollock, N. Hayward, J. Palmer, 1997, Oncogene.

Loss of expression of the p16/cyclin-dependent kinase inhibitor 2 tumor suppressor gene in melanocytic lesions correlates with invasive stage of tumor progression.

F. Haluska, C. Shea, F. Loganzo, 1995, Cancer research.

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations

P. Pollock, W. Foulkes, N. Hayward, 1998, Human mutation.

Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.

N. Hayward, F. Haluska, N. Dracopoli, 1995, Human molecular genetics.

Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.

D. Ledbetter, P. O'Connell, R. White, 1989, American journal of human genetics.

Loss of the p16INK4a and p15INK4b genes, as well as neighboring 9p21 markers, in sporadic melanoma.

M. Bulyk, D. Housman, N. Hayward, 1996, Cancer research.

CEPH consortium Map of chromosome 9.

J. Haines, J. Attwood, J. Gusella, 1994, Genomics.

Report of the Second International Workshop on Human Chromosome 9 Mapping 1993

J. Haines, M. Pericak-Vance, S. Povey, 1993 .

Oncogenes and Tumor Suppressor Genes in Cutaneous Malignant Melanoma

A. Albino, J. Fountain, 1996, Photochemistry and photobiology.

Report and abstracts of the First International Workshop on Chromosome 9. Held at Girton College Cambridge, UK, 22-24 March, 1992.

S. Povey, D. Kwiatkowski, I. Jackson, 1992, Annals of human genetics.

REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22–24 March, 1992

S. Povey, D. Kwiatkowski, I. Jackson, 1992 .

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).

D. Housman, E. Petty, T. Yang-Feng, 1993, American journal of human genetics.

CDKN2 mutations in melanoma.

N. Dracopoli, J. Fountain, 1996, Cancer surveys.

Genetics of melanoma.

D. Housman, S. Bale, N. Dracopoli, 1990, Cancer surveys.

Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomes.

F. Collins, M. Wallace, J. Fountain, 1989, Nucleic acids research.

The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations.

D. Ledbetter, P. O'Connell, M. Culver, 1990, Genomics.

Homozygous Loss of the @15INK4BGene (and not the @16@4K4Gene) during Tumor Progression in a Sporadic Melanoma Patient1

A. Albino, S. Stone, G. Walker, 2006 .

Loss of the pJ 6 INK 4 aand @ 15 INK 4 bGenes , as well as Neighboring 9 p 2 i Markers , in Sporadic Melanoma 1

M. Bulyk, D. Housman, N. Hayward, 2022 .

Molecular genetics of human malignant melanoma.

A. Albino, J. Fountain, 1993, Cancer treatment and research.

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients.

B. Brownstein, M. Wallace, L. B. Andersen, 1990, Science.

Low frequency of p16/CDKN2A methylation in sporadic melanoma: comparative approaches for methylation analysis of primary tumors.

N. Hayward, P. Jones, M. Gonzalgo, 1997, Cancer research.

Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22.

M. Skolnick, C. Lewis, O. Olopade, 1992, Science.

Homozygous deletions within human chromosome band 9p21 in melanoma.

J. Kirkwood, M. Karayiorgou, A. Houghton, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Homozygous loss of the p15INK4B gene (and not the p16INK4 gene) during tumor progression in a sporadic melanoma patient.

A. Albino, S. Stone, G. Walker, 1995, Cancer research.

Virtually 100% of melanoma cell lines harbor alterations at the DNA level within CDKN2A, CDKN2B, or one of their downstream targets

G. Walker, J. Flores, J. Glendening, 1998, Genes, chromosomes & cancer.

Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia.

O. Olopade, D. Housman, G. Robertson, 1994, Cancer research.

Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

F. Collins, D. Housman, D. Gutmann, 1993, Nature Genetics.

Genetic and physical map of the interferon region on chromosome 9p.

D. Housman, D. Ward, M. Karayiorgou, 1992, Genomics.

Identification of a novel region of homozygous deletion on chromosome 9p in squamous cell carcinoma of the lung: the location of a putative tumor suppressor gene.

W. Franklin, D. Sidransky, R. Gemmill, 1997, Cancer research.

Localization of multiple melanoma tumor-suppressor genes on chromosome 11 by use of homozygosity mapping-of-deletions analysis.

N. Hayward, G. Walker, J. Glendening, 2000, American journal of human genetics.

PTEN inactivation is rare in melanoma tumours but occurs frequently in melanoma cell lines

P. Pollock, N. Hayward, J. Glendening, 2002, Melanoma research.

In vitro loss of heterozygosity targets the PTEN/MMAC1 gene in melanoma.

W. Cavenee, F. Furnari, H. Huang, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Functional localization of a melanoma tumor suppressor gene to a small (≤2 Mb) region on 11q23

G. Robertson, J. Fountain, T. Lugo, 1999, Oncogene.

Transfection of primary human skin fibroblasts by electroporation.

F. Collins, W. K. Lockwood, J. Fountain, 1988, Gene.

(Transient expression; CAT assay; stable integration; neomycin resistance; calcium phosphate transformation)

F. Collins, W. K. Lockwood, J. Fountain, 1988 .

Physical mapping of a translocation breakpoint in neurofibromatosis.

F. Collins, J. Gusella, B. Seizinger, 1989, Science.

Markers and tissue resources for melanoma: meeting report.

V. Sondak, M. Mihm, S. Hewitt, 2006, Cancer research.

Linkage mapping of the Aldo-2, Pax-5, Ambp, and D4h9S3E loci on mouse chromosome 4 in the region of homology with human chromosome 9.

C. Abbott, J. Peters, J. Fountain, 1993, Genomics.

FineStructure DNA Mapping Studies oftheChromosomal Region Harboring theGenetic Defect in Neurofibromatosis TypeI

D. Ledbetter, M. Leppert, P. O'Connell, 1989 .