U. Bengtsson

发表

Sticky Anaphase Aberrations after G2-Phase Arrest of Gamma-Irradiated Human Skin Fibroblasts: TP53 Independence of Formation and TP53 Dependence of Consequences

E. Stanbridge, J. Redpath, U. Bengtsson, 2003, Radiation research.

Malignant transformation of human diploid fibroblasts and suppression of their anchorage independence by introduction of chromosome 13

M. Yutsudo, A. Hakura, E. Stanbridge, 1999, Genes, chromosomes & cancer.

Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.

D. Skarecky, U. Bengtsson, N. Carpenter, 1988, American journal of human genetics.

Complexity of the Mechanisms of Initiation and Maintenance of DNA Damage-Induced G2-Phase Arrest and Subsequent G1-Phase Arrest: TP53-Dependent and TP53-Independent Roles

E. Stanbridge, J. Redpath, U. Bengtsson, 2003, Radiation research.

Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy

U. Bengtsson, M. Altherr, S. Winokur, 1995, Muscle & nerve. Supplement.

S. Brant, J. Wasmuth, U. Bengtsson, 1996, Mammalian genome : official journal of the International Mammalian Genome Society.

Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer

B. Roe, M. Sawicki, E. Stanbridge, 2002, Oncogene.

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.

N. Freimer, T. Gilliam, C. Kaufmann, 1989, Genomics.

Interstitial deletion of 11q13 sequences in HeLa cells

E. Stanbridge, J. Redpath, U. Bengtsson, 2000, Genes, chromosomes & cancer.

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome.

J. Wasmuth, U. Bengtsson, J. Overhauser, 1994, Human molecular genetics.

Characterization of the murine homolog of C1qR(P): identical cellular expression pattern, chromosomal location and functional activity of the human and murine C1qR(P).

U. Bengtsson, S. Winokur, A. Tenner, 2000, Molecular immunology.

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.

D. Ledbetter, J. Gusella, J. Wasmuth, 1991, American journal of human genetics.

Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.

J. Wasmuth, U. Bengtsson, J. Ulm, 1989, American journal of human genetics.

Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features.

D. Church, K. Nielsen, J. Wasmuth, 1995, American journal of human genetics.

Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization.

J. Wasmuth, U. Bengtsson, M. Bocian, 1993, American journal of medical genetics.

High resolution physical map of the region surrounding the spinal muscular atrophy gene.

J. McPherson, T. Gilliam, K. Davies, 1993, Human molecular genetics.

Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?

U. Bengtsson, S. Winokur, S. M. van der Maarel, 2004, Human molecular genetics.

A functional investigation of tumor suppressor gene activities in a nasopharyngeal carcinoma cell line HONE1 using a monochromosome transfer approach

M. Lerman, E. Stanbridge, M. Lung, 2000, Genes, chromosomes & cancer.

The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region.

J. Wasmuth, U. Bengtsson, M. Altherr, 1996, Human molecular genetics.

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease

K. Mathews, J. Wasmuth, J. Murray, 1994, Chromosome Research.

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.

J. Wasmuth, U. Bengtsson, M. Altherr, 1994, Human molecular genetics.

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei

M. Ehrlich, U. Bengtsson, Jennifer T. Stocksdale, 2010, European Journal of Human Genetics.

High-resolution physical mapping of human 5q31-q33 using three methods: radiation hybrid mapping, interphase fluorescence in situ hybridization, and pulsed-field gel electrophoresis.

J. Warrington, U. Bengtsson, 1994, Genomics.

S. Brant, J. Wasmuth, U. Bengtsson, 1996, Mammalian Genome.

Analysis of aberrant methylation of the VHL gene by transgenes, monochromosome transfer, and cell fusion

F. Duh, M. Lerman, E. Stanbridge, 1999, Oncogene.

Assignment of the cysteinyl-tRNA synthetase gene (CARS) to 11p15.5.

S. Arfin, J. Wasmuth, U. Bengtsson, 1993, Genomics.