Significance of chromosome 1p loss of heterozygosity in neuroblastoma

JM Maris, PS White, CP Beltinger, EP Sulman… - Cancer research, 1995 - AACR
We analyzed 156 primary neuroblastoma tumor samples for loss of heterozygosity at the
distal short arm of chromosome 1 (1p LOH). We also compared 1p LOH with known clinical …

Physical Mapping and Genomic Structure of the HumanTNFR2Gene

CP Beltinger, PS White, JM Maris, EP Sulman… - Genomics, 1996 - Elsevier
The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region
characteristically deleted in neuroblastomas and other malignancies. In addition, TNFR2 is …

Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma

PS White, JM Maris, EP Sulman, SJ Jensen… - European Journal of …, 1997 - Elsevier
Cellular, cytogenetic, and molecular evidence indicates that chromosome band 1p36 is
often deleted in neuroblastoma cell lines and tumours, suggesting the presence of one or …

Human Krüppel-related 3 (HKR3): a candidate for the 1p36 neuroblastoma tumour suppressor gene?

JM Maris, J Jensen, EP Sulman, CP Beltinger… - European Journal of …, 1997 - Elsevier
Human Krüppel-related 3 (HKR3) is a zinc finger gene that maps within chromosome
subbands 1p36. 2-. 3, a region postulated to contain a tumour suppressor gene associated …

Cloning, Chromosomal Localization, Physical Mapping, and Genomic Characterization ofHKR3

JM Maris, SJ Jensen, EP Sulman, CP Beltinger… - Genomics, 1996 - Elsevier
TheKrüppel-type zinc finger proteins are members of a conserved family of transcription
factors that are important in developmental regulation. Altered expression of several of these …

No CDKN2 Mutations in Neuroblastomas

CP Beltinger, PS White, EP Sulman, JM Maris… - Cancer research, 1995 - AACR
Mutations of CDKN2 have been found recently in melanoma and many other tumor types.
Neuroblastoma shares with melanoma a neuroectodermal origin and a high incidence of …

A simple combined microdissection and aspiration device for the rapid procurement of single cells from clinical peripheral blood smears.

CP Beltinger, KM Debatin - Molecular Pathology, 1998 - ncbi.nlm.nih.gov
Molecular analysis of cells from cytology specimens can help to establish a diagnosis in
ambiguous cases. However, mutations in heterogeneous samples might not be detected …

Whole genome amplification of single cells from clinical peripheral blood smears.

CP Beltinger, F Klimek, KM Debatin - Molecular Pathology, 1997 - ncbi.nlm.nih.gov
Molecular analysis of clinical samples has been hampered by the lack of fresh or frozen
specimens and the presence of contaminating background cells within samples obscuring …

[CITATION][C] UPTAKE MECHANISMS AND INTRACELLULAR TRAFFICKING OF PHOSPHOROTHIOATE MODIFIED OLIGODEOXYNUCLEOTIDES

CP Beltinger, RM Smith, HU Sargovi… - …, 1993 - WB SAUNDERS CO …