Report of the committee on chromosome and gene loss in human neoplasia

Bernd R. Seizinger, H.P. Klinger, Claudine Junien, +14

Cytogenetic and Genome Research

Cancer PathologyCytogeneticsHuman NeoplasiaGeneticsMedicine +7

Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma.

Ryoji Morita, S. Saito, Jiro ISHIKAWA, +4

PubMed

CytogeneticsGeneticsRenal PathologyPathologyAllelic Losses +16

A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma.

Kazuhiro Yamakawa, Ryoji Morita, Ei Takahashi, +3

PubMed

Detailed Deletion MappingChromatinShort ArmUrologyChromosome 3P21.3 +13

Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR)

Susumu Saito, Aritoshi Iida, Akihiro Sekine, +5

Journal of Human Genetics

Molecular PhysiologyAtp-binding CassetteNatural SciencesGeneticsProtein Genetics +8

Somatic Mutations of the MTS (Multiple Tumor Suppressor) 1/CDK41 (Cyclin-Dependent Kinase-4 Inhibitor) Gene in Human Primary Non-small Cell Lung Carcinomas

Naoko Hayashi, Yoshihisa Sugimoto, Eiju Tsuchiya, +2

Biochemical and Biophysical Research Communications

Somatic VariantSomatic MutationsMultiple Tumor SuppressorMedicinePathology +8

Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia

Marcel M. A. M. Mannens, J.M.N. Hoovers, E. Redeker, +20

European Journal of Human Genetics

Beckwith-wiedemann SyndromeGenetic DisorderGeneticsPathologyMolecular Genetics +6

Mutagenic/carcinogenic potential of DEHP and MEHP.

Ikuyoshi Tomita, Y. Nakamura, Noboru Aoki, +1

Environmental Health Perspectives

Transgenic TechnologySyrian Golden HamsterMedicineGeneticsPathology +10

Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population

Susumu Saito, Aritoshi Iida, Akihiro Sekine, +4

Journal of Human Genetics

BiologyAllelic VariantHaplotype DeterminationGenetic DisorderNatural Sciences +9

Aberrant upregulation of a novel integrin alpha subunit gene at 3p21.3 in small cell lung cancer.

K Hibi, Kazuhiro Yamakawa, Ryuzo Ueda, +6

PubMed

Genetic linkage between Von Hippel—Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus

Paul A. Crossey, Eamonn R. Maher, Michael H. Jones, +15

Human Molecular Genetics