Search Results - "Wilgenbus, K K"
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DMBT1 , a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours
Published in Nature genetics (01-09-1997)“…Loss of sequences from human chromosome 10q has been associated with the progression of human cancer. Medulloblastoma and glioblastoma multiforme are the most…”
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CDNA microarray gene expression analysis of B‐cell chronic lymphocytic leukemia proposes potential new prognostic markers involved in lymphocyte trafficking
Published in International journal of cancer (15-02-2001)“…Human cancer is characterized by complex molecular perturbations leading to variable clinical behavior, often even in single‐disease entities. We performed a…”
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3
Expression of Cx26, Cx32 and Cx43 gap junction proteins in normal and neoplastic human tissues
Published in International journal of cancer (19-06-1992)“…This report concerns the expression of the gap-junction proteins Connexin (Cx)26, 32 and 43 in different malignant and non-malignant human tissues…”
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4
DNA chip technology ante portas
Published in Journal of molecular medicine (Berlin, Germany) (01-11-1999)“…The recent popularity of DNA chip technology has been fostered by the increasing demand for new diagnostic tools which allow the simultaneous analysis of large…”
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Mapping of chromosomal imbalances in gastric adenocarcinoma revealed amplified protooncogenes MYCN, MET, WNT2, and ERBB2
Published in Genes chromosomes & cancer (01-12-1998)“…Gastric adenocarcinoma is a malignant tumor with a high incidence and a low survival rate. In order to identify genetic alterations associated with this tumor,…”
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Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics
Published in Cytogenetics and cell genetics (01-01-2000)“…Leiomyosarcomas comprise a group of malignant soft-tissue tumors with smooth-muscle differentiation. In this study, 14 cases of leiomyosarcoma were screened…”
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7
Radixin is a component of hepatocyte microvilli in situ
Published in Experimental cell research (01-01-1994)Get more information
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Molecular Characterization of a Genetically Unstable Region Containing the SMS Critical Area and a Breakpoint Cluster for Human PNETs
Published in Genomics (San Diego, Calif.) (15-05-1997)“…Recently we demonstrated the clustering of deletion breakpoints in the pericentromeric region of human chromosome 17p in human primitive neuroectodermal tumors…”
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High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2
Published in Genes chromosomes & cancer (01-01-1997)“…Loss of heterozygosity (LOH) on chromosome arm 17p is the most common genetic aberration in childhood primitive neuroectodermal tumors (PNETs). To determine…”
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10
Molecular cloning, cDNA sequence, and chromosomal assignment of the human radixin gene and two dispersed pseudogenes
Published in Genomics (San Diego, Calif.) (01-04-1993)“…Radixin is a cytoskeletal protein that may be important in linking actin to the plasma membrane. Recent cloning of the murine and porcine radixin cDNAs…”
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Acute lethal necrotising pancreatitis in childhood systemic lupus erythematosus--possible toxicity of immunosuppressive therapy
Published in Clinical and experimental rheumatology (01-05-1995)“…We report on a 16 year old girl with a three-year history of systemic lupus erythematosus who developed a case of acute lethal haemorrhagic pancreatitis. She…”
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12
Two fetuses with Fryns syndrome without diaphragmatic defects
Published in Journal of medical genetics (01-12-1994)“…We report two fetuses with Fryns syndrome including the typical facial appearance and distal limb and lung hypoplasia, but no diaphragmatic hernias. The…”
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13
Further evidence that acanthosis nigricans maligna is linked to enhanced secretion by the tumour of transforming growth factor alpha
Published in Archives of Dermatological Research (01-09-1992)“…The pathogenesis of cutaneous paraneoplastic syndromes is still under discussion. Since many of these syndromes, including acanthosis nigricans, are…”
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14
Structure and localization on the X chromosome of the gene coding for the human filopodial protein moesin (MSN)
Published in Genomics (San Diego, Calif.) (15-01-1994)“…Moesin is a member of a recently discovered family of closely related proteins that includes ezrin, radixin, and merlin. It is widely expressed in different…”
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Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1
Published in Cytogenetics and cell genetics (01-01-1996)“…Sixty-four PCR-markers previously assigned to the short arm of chromosome 17 and two newly established STSs were localized on a hybrid cell-YAC clone panel…”
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Correlation of clinical data with proteomics profiles in 24 patients with B‐cell chronic lymphocytic leukemia
Published in International journal of cancer (15-01-2001)“…The development of human cancer is caused by complex molecular perturbations leading to variable clinical behavior often even in single disease entities. To…”
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17
Gene expression profiling in drug discovery and development
Published in Current opinion in molecular therapeutics (01-12-1999)“…Recent advances in technology, especially the merger between molecular biology, automation technology and computer science, are rapidly changing the manner in…”
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Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)
Published in Genes chromosomes & cancer (01-07-1999)“…Isochromosomes are monocentric or dicentric chromosomes with homologous arms that are attached in a reverse configuration as mirror images. With an incidence…”
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The impact of DNA chip technology on molecular medicine
Published in Arthritis research (26-01-2001)Get full text
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Eye changes in acanthosis nigricans maligna--possible effect of growth factors in the etiopathogenesis of this paraneoplastic disease picture
Published in Klinische Monatsblätter für Augenheilkunde (01-09-1992)“…A 64-year-old white male presented to our hospital with hyperplastic tarsal and to a lesser degree bulbar conjunctivae. Approximately one month later the full…”
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