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Featured researches published by Steven D. Colman.


Genes, Chromosomes and Cancer | 2000

Chromosome 17 loss‐of‐heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1

Sonja A. Rasmussen; Jennifer Overman; Susanne A. M. Thomson; Steven D. Colman; C. R. Abernathy; Rachael E. Trimpert; Rebecca Moose; Gurinder Virdi; Kyle J. Roux; Mislen Bauer; Amyn M. Rojiani; Bernard L. Maria; David Muir; Margaret R. Wallace

Neurofibromatosis type 1 (NF1) is a common autosomal dominant condition characterized by benign tumor (neurofibroma) growth and increased risk of malignancy. Dermal neurofibromas, arising from superficial nerves, are primarily of cosmetic significance, whereas plexiform neurofibromas, typically larger and associated with deeply placed nerves, extend into contiguous tissues and may cause serious functional impairment. Malignant peripheral nerve sheath tumors (MPNSTs) seem to arise from plexiform neurofibromas. The NF1 gene, on chromosome segment 17q11.2, encodes a protein that has tumor suppressor function. Loss of heterozygosity (LOH) for NF1 has been reported in some neurofibromas and NF1 malignancies, but plexiform tumors have been poorly represented. Also, the studies did not always employ the same markers, preventing simple comparison of the frequency and extent of LOH among different tumor types. Our chromosome 17 LOH analysis in a cohort of three tumor types was positive for NF1 allele loss in 2/15 (13%) dermal neurofibromas, 4/10 (40%) plexiform neurofibromas, and 3/5 (60%) MPNSTs. Although the region of loss varied, the p arm (including TP53) was lost only in malignant tumors. The losses in the plexiform tumors all included sequences distal to NF1. No subtle TP53 mutations were found in any tumors. This study also reports the identification of both NF1 “hits” in plexiform tumors, further supporting the tumor suppressor role of the NF1 gene in this tumor type. Genes Chromosomes Cancer 28:425–431, 2000.


Mammalian Genome | 1996

A multiplex-PCR test for EVI2A and EVI2B polymorphisms within the human NF1 gene

Sonja A. Rasmussen; V. T. Ho; Steven D. Colman; C. R. Abernathy; Margaret R. Wallace

~Department of Pediatrics, Division of Genetics, Box 100296, University of Florida College of Medicine, Gainesville, Florida 32610-0296, USA 2Department of Biochemistry and Molecular Biology, University of Florida College of Medicine, Gainesville, Florida 32610, USA 3Department of Pathology and Laboratory Medicine, University of Florida College of Medicine, Gainesville, Florida 32610, USA 4Center for Mammalian Genetics, University of Florida College of Medicine, Gainesville, Florida 32610, USA


Nature Genetics | 1995

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene

Steven D. Colman; Charles A. Williams; Margaret R. Wallace


Human Molecular Genetics | 1997

Identification of Mutations in Two Major mRNA Isoforms of the Chediak-Higashi Syndrome Gene in Human and Mouse

Maria D. F. S. Barbosa; Franck J. Barrat; Velizar T. Tchernev; Quan A. Nguyen; Vishnu S. Mishra; Steven D. Colman; Elodie Pastural; Rémi Dufourcq-Lagelouse; Alain Fischer; Randall F. Holcombe; Margaret R. Wallace; Stephen J. Brandt; Geneviève de Saint Basile; Stephen F. Kingsi'mora


Human Mutation | 1994

Two NF1 mutations: Frameshift in the GAP-related domain, and loss of two codons toward the 3′ end of the gene

C. R. Abernathy; Steven D. Colman; Boris G. Kousseff; Margaret R. Wallace


Clinical Genetics | 2008

A PCR-based test for a polymorphism within the human NF1 gene

C. R. Abernathy; Steven D. Colman; Margaret R. Wallace


Archive | 2002

Proteins, polynucleotides ecoding them and methods of using the same

David W. Anderson; Catherine E. Burgess; Stacie J. Casman; Steven D. Colman; Shlomit R. Edinger; Karen Ellerman; Valerie Gerlach; Erik Gunther; Ramesh Kekuda; John R. Macdougall; Fuad Mehraban; Meera Patturajan; Mark E. Rothenberg; Richard A. Shimkets; Glennda Smithson; Kimberly A. Spytek; David J. Stone; Corine A. M. Vernet; Bryan D. Zerhusen


Archive | 2001

Novel nucleic acids and polypeptides and methods of use thereof

Richard A. Shimkets; Meera Patturajan; Corine A. M. Vernet; Stacie J. Casman; Uriel M. Malyankar; Suresh G. Shenoy; Kimberly A. Spytek; Esha A. Gangolli; Charles E. Miller; Ferenc L. Boldog; Li Li; Raymond J. Taupier; Ramesh Kekuda; Glennda Smithson; Bryan D. Zerhusen; Xiaohong Liu; Steven D. Colman; Velizar T. Tchernev; Jingsheng Si; Shlomit R. Edinger; David A. Stone; Paul Sciore; Isabelle Millet; Mark Rothenberg


Somatic Cell and Molecular Genetics | 1992

Isolation and characterization of radiation-reduced hybrids containing portions of the proximal long arm of the human X chromosome : identification of hybrids containing the Menkes' disease locus

Steven D. Colman; Jane K. Mellott; Alison S. Almeida; Michael A. Goldman; Peter Van Tuinen; Thomas P. Yang


Archive | 2002

Novel protein and nucleic acids encoding same

Li Li; Muralidhara Padigaru; Robert A. Ballinger; Ramesh Kekuda; Steven D. Colman; Paul Sciore; Glennda Smithson; John A. Peyman; John R. Macdougall; David A. Stone; Corine A. M. Vernet; Suresh G. Shenoy; Erik Gunther; Isabelle Millet; Velizar T. Tchernev; David W. Anderson; Vladimir Gusev; Uriel M. Malyankar; Haihong Zhong; Karen Ellerman; Adam R. Wolenc

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Suresh G. Shenoy

Case Western Reserve University

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David A. Stone

Case Western Reserve University

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