Paul S. Thorner

发表

Tyrosine phosphorylation in human lymphomas

A. Rosenwald, E. Campo, G. Ott, 2004, The Histochemical Journal.

Prognostic impact of chromosomal aberrations in Ewing tumours

S. Knuutila, P. Ambros, J. Squire, 2002, British Journal of Cancer.

Analysis of Segmental Duplications, Mouse Genome Synteny and Recurrent Cancer-Associated Amplicons in Human Chromosome 6p21–p12

Paulo A. S. Nuin, O. Ludkovski, J. Squire, 2010, Cytogenetic and Genome Research.

Prognostic significance of age, MYCN oncogene amplification, tumor cell ploidy, and histology in 110 infants with stage D(S) neuroblastoma: the pediatric oncology group experience--a pediatric oncology group study.

A. Look, G. Brodeur, S. Cohn, 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Multidrug Resistance: Clinical Opportunities in Diagnosis and Circumvention

B. Gallie, V. Ling, G. Deboer, 1994 .

Erosive adenomatosis of the nipple in an eight-year-old girl.

P. Thorner, B. Krafchik, S. E. Albers, 1999, Journal of the American Academy of Dermatology.

Molecular Genetics in the Diagnosis and Prognosis of Solid Pediatric Tumors

J. Squire, P. Thorner, Jeremy A. Squire, 1998, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Bilateral congenital midureteral adynamic segments.

B. Churchill, P. Thorner, A. Khoury, 1995, Urology.

Detection of global hypermethylation in well-differentiated thyroid neoplasms by immunohistochemical (5-methylcytidine) analysis

P. Thorner, N. Kitkumthorn, A. Mutirangura, 2015, Journal of Endocrinological Investigation.

High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalin-fixed paraffin-embedded tissue

J. Squire, J. Bayani, B. Beheshti, 2004, Cytogenetic and Genome Research.

Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH

O. Ludkovski, J. Squire, J. Bayani, 2008, Cytogenetic and Genome Research.

Application of comparative genomic hybridization, spectral karyotyping, and microarray analysis in the identification of subtype-specific patterns of genomic changes in rhabdomyosarcoma.

J. Squire, R. Godbout, J. Bayani, 1999, Neoplasia.

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV.

R. Mcinnes, P. Thorner, P. Marrano, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Co-amplification of MYCN and a DEAD box gene (DDX1) in primary neuroblastoma.

S. Weitzman, J. Squire, R. Godbout, 1995, Oncogene.