Jahresbibliographie 1996

Veröffentlichungen von
Angehörigen der Hochschulen des Saarlandes

FR 3.9 - Humangenetik

Dooley, Steven
- u.a.: c-myb intron I protein binding and its association with
transcriptional activity in leukemic cells. - In: Leukemia Research. - 20
(1996), S. 429-439
 
- u.a.: Constitutive expression of c-fos and c-jun, overexpression of ets-2
and reduced expression of metastasis suppressor gene nm23-H1 in rheumatoid
arthritis. - In: Annals of Rheumatic Diseases. - 55 (1996), S. 298-304
 
- u.a.: Isolation and characterization of the human mismatch repair gene
hMSH2 promoter region. - In: Human Genetics. - 97 (1996), S. 114-116
 
- u.a.: A second trefoil protein, itf/hp1.b, is transcribed in human breast
cancer. - In: Breast Cancer Research and Treatment. - 38 (1996), 2, S. 145-151
 
- u.a.: Specific in vitro binding of p53 to the promoter region of the human
mismatch repair gene hmsh2. - In: Biochemical Biophysical Research
Communications. - 221 (1996), S. 722-728
 
Ermis, Ayhan
- u.a.: Constitutive expression of c-fos and c-jun, overexpression of ets-2
and reduced expression of metastasis suppressor gene nm23-H1 in rheumatoid
arthritis. - In: Annals of Rheumatic Diseases. - 55 (1996), S. 298-304
 
Fischer, Ulrike
- u.a.: Amplification of the MET Gene in Glioma. - In: Genes, Chromosomes &
Cancer. - 12 (1995), 1, S. 63-65
 
- u.a.: Amplification on chromosomes 1p31, 1q21-24,5p13-14, and 11p12-14 in
ovarian carcinoma detected by reverse chromosome painting. - In: Oncology
Reports. - 1 (1994), S. 1069-1073
 
- u.a.: Comparative amplification analysis of human glioma and tumor
fragment spheroid using reverse chromosome painting (RCP). - In: Anticancer
Research. 1996
 
- u.a.: DNA amplifications on chromosomes 7, 9 and 12 in glioblastoma
detected by reverse chromosome painting. - In: European Journal of Cancer. -
30A (1994), 8, S. 1124-1127
 
- u.a.: Isolation and localization of transcribed sequences on human
chromosome 22. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 81-85
 
- u.a.: Isolation of Genes amplified in Human Cancers by Microdissection
mediated cDNA capture. - In: Human Molecular Genetics. - 5 (1996), S. 595-600
 
Göttert, Elisabeth
- u.a.: DNA amplifications on chromosomes 7, 9 and 12 in glioblastoma
detected by reverse chromosome painting. - In: European Journal of Cancer. -
30A (1994), 8, S. 1124-1127
 
- u.a.: Enrichment of chromosome specific hncDNAs by magnetic beads. - In:
Molecular Biology Reports. - 22 (1996), S. 53-57
 
- u.a.: Human endogenous retroviral element k10 (HERV-K10): chromosomal
localization by somatic hybrid mapping and fluorescence in situ hybridization.
- In: Cytogenetics and Cell Genetics. - 72 (1996), S. 40-42
 
- u.a.: Isolation and localization of transcribed sequences on human
chromosome 22. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 81-85
 
- u.a.: Isolation of human chromosome 6 specific hncDNA clones from a
somatic hybrid cDNA library. - In: Cytogenetics and Cell Genetics. - 69
(1995), S. 273-278
 
Henn, Wolfram
- u.a.: Chromosomal findings and p53 mutation analysis in chromophilic renal
cell carcinomas. - In: Internat. journal of cancer. - 68 (1996), S. 47-50
 
- u.a.: Constitutive expression of c-fos and c-jun, overexpression of ets-2
and reduced expression of metastasis suppressor gene nm23-H1 in rheumatoid
arthritis. - In: Annals of Rheumatic Diseases. - 55 (1996), S. 298-304
 
- u.a.: Correlation between cytogenetic and clinical findings in 215 human
meningiomas. - In: Acta Neurochirurgica. - Suppl. 65 (1996), S. 73-76
 
- u.a.: Early Proliferation Enhancement by Monosomy 10 and Intratumoral
Heterogeneity in Malignant Human Gliomas as Revealed by Smear Preparations
From Biopsies. - In: Genes, Chromosomes & Cancer. - 16 (1996), S. 180-184
 
- Ethical aspects of premarital genetic screening. - In: Human Heredity. -
46 (1996), S. 342
 
- Ethische Aspekte einer Diagnostik zur Voraussage erblicher Erkrankungen. -
In: Saarländisches Ärzteblatt. - 49 (1996), 10, S. 15-17
 
- u.a.: Frequent Homozygous Loss of p16 and Loss of Heterozygosity of p53 in
Gliomas as Detected by Two-colour In situ Hybridization. - In: Zentralbl
Neurochir. 1996, Suppl, S. 90
 
- u.a.: Genetic heterogeneity of CDKN2 and p53 in human gliomas. - In:
Journal of Neuro-Oncology. - 30 (1996), 2, S. 110
 
- Internet: Neue Möglichkeiten unterschätzt. - In: Deutsches Ärzteblatt. -
1996 (1996), 93, S. A146
 
- u.a.: Malignant melanoma in a patient with EEC syndrome. - In:
Medizinische Genetik. - 1996 (1996), 1, S. 85
 
- u.a.: Metanephroider Nierentumor - Morphologie, Genetik und Prognose. -
In: Verhandlungen der Deutschen Ges. für Pathologie. - 80 (1996), S. 641
 
- u.a.: Microdeletions in cleidocranial dysplasia. - In: American journal of
human genetics. - 59 (1996), S. A274
 
- u.a.: Microdissection of Chromosomes - A Rapid Method for the
Identification of Prognostically Relevant Chromosomal Anomalies in Brain
Tumors. - In: Zentralbl Neurochir. 1996, Suppl, S. 93
 
- u.a.: A novel site of DNA amplification on chromosome 1p32-33 in a
rhabdomyosarcoma revealed by comparative genomic hybridization. - In: Human
Genetics. - 97 (1996), S. 87-90
 
Klein, Veronika
- u.a.: Isolation and localization of transcribed sequences on human
chromosome 22. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 81-85
 
Meese, Eckart
- u.a.: Amplification of the MET Gene in Glioma. - In: Genes, Chromosomes &
Cancer. - 12 (1995), 1, S. 63-65
 
- u.a.: Amplification on chromosomes 1p31, 1q21-24,5p13-14, and 11p12-14 in
ovarian carcinoma detected by reverse chromosome painting. - In: Oncology
Reports. - 1 (1994), S. 1069-1073
 
- u.a.: Amplified DNA sequences on chromosome 3q26.3 in squamous cell
carcinoma of the lung by one colour Comparative Genomic Hybridisation. - In:
European Journal of Cancer. - 32A (1996), S. 1205-1208
 
- u.a.: Assignment of Alu-repetitive sequences to large restriction
fragments from human chromosomes 6 and 22. - In: Molecular Biology Reports. -
21 (1995), S. 81-84
 
- u.a.: Comparative amplification analysis of human glioma and tumor
fragment spheroid using reverse chromosome painting (RCP). - In: Anticancer
Research. 1996
 
- u.a.: Debrisoquine hydroxylase gene polymorphism in meningioma. - In: Acta
Neuropathologica. - 88 (1994), S. 472-474
 
- u.a.: DNA amplifications on chromosomes 7, 9 and 12 in glioblastoma
detected by reverse chromosome painting. - In: European Journal of Cancer. -
30A (1994), 8, S. 1124-1127
 
- Double Minutes in the Papillary Thyroid Cancer Cell Line PTC-1113A. - In:
Cancer GeneticsCytogenetics. - 90 (1996), S. 70-74
 
- u.a.: Enrichment of chromosome specific hncDNAs by magnetic beads. - In:
Molecular Biology Reports. - 22 (1996), S. 53-57
 
- u.a.: Human endogenous retroviral element k10 (HERV-K10): chromosomal
localization by somatic hybrid mapping and fluorescence in situ hybridization.
- In: Cytogenetics and Cell Genetics. - 72 (1996), S. 40-42
 
- u.a.: Isolation and localization of transcribed sequences on human
chromosome 22. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 81-85
 
- u.a.: Isolation of Genes amplified in Human Cancers by Microdissection
mediated cDNA capture. - In: Human Molecular Genetics. - 5 (1996), S. 595-600
 
- u.a.: Isolation of human chromosome 6 specific hncDNA clones from a
somatic hybrid cDNA library. - In: Cytogenetics and Cell Genetics. - 69
(1995), S. 273-278
 
- u.a.: Lack of uniparental isodisomy for chromosome 22 in disomic
meningiomas. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 139-141
 
- Regional Localization of over 300 Loci on Human Chromosome 22 Using a
Somatic Cell Hybrid Mapping Panel. - In: Genomics. - 35 (1996), S. 275-288
 
- u.a.: Molecular Screening for RET Proto-Oncogene Mutations in a German MEN
2A Pedigree. - In: Clinical Research; Endocrine Pathology. - 7 (1996), 1, S.
71-76
 
Müller, Hans-Werner
- u.a.: Amplification of the MET Gene in Glioma. - In: Genes, Chromosomes &
Cancer. - 12 (1995), 1, S. 63-65
 
- u.a.: Assignment of Alu-repetitive sequences to large restriction
fragments from human chromosomes 6 and 22. - In: Molecular Biology Reports. -
21 (1995), S. 81-84
 
- u.a.: Enrichment of chromosome specific hncDNAs by magnetic beads. - In:
Molecular Biology Reports. - 22 (1996), S. 53-57
 
- u.a.: Isolation of human chromosome 6 specific hncDNA clones from a
somatic hybrid cDNA library. - In: Cytogenetics and Cell Genetics. - 69
(1995), S. 273-278
 
Oehl-Jaschkowitz, Barbara
- u.a.: Partielle Trisomie 1q. - In: Monatsschr. Kinderheilkunde, Suppl. 1. -
144 (1996), 8 (P 518)
 
Welter, Cornelius
- u.a.: c-myb intron I protein binding and its association with
transcriptional activity in leukemic cells. - In: Leukemia Research. - 20
(1996), S. 429-439
 
- u.a.: Constitutive expression of c-fos and c-jun, overexpression of ets-2
and reduced expression of metastasis suppressor gene nm23-H1 in rheumatoid
arthritis. - In: Annals of Rheumatic Diseases. - 55 (1996), S. 298-304
 
- u.a.: Differential expression of heat shock protein 70 in well healing and
chronic human wound tissue. - In: Biochem Biophys Res Commun. - 214 (1995), S.
1009-1014
 
- u.a.: Genetische Aspekte bei Gastrointestinaltumoren. - Thieme, 1996, S.
31O-316. - (Klinische Gastroenterologie)
 
- u.a.: Inhibition of nucleoside diphosphate kinase activity by in vitro
phosphorylation by protein kinase CK2. - In: FEBS Letters. - 399 (1996), S.
183-187
 
- u.a.: Isolation and characterization of the human mismatch repair gene
hMSH2 promoter region. - In: Human Genetics. - 97 (1996), S. 114-116
 
- u.a.: A second trefoil protein, itf/hp1.b, is transcribed in human breast
cancer. - In: Breast Cancer Research and Treatment. - 38 (1996), 2, S. 145-151
 
- u.a.: Specific in vitro binding of p53 to the promoter region of the human
mismatch repair gene hmsh2. - In: Biochemical Biophysical Research
Communications. - 221 (1996), S. 722-728
 
- u.a.: A third P-domain peptide gene (human intestinal trefoil factor) maps
to 21q22.3. - In: Cytogenetics and Cell Genetics. - 72 (1996), S. 299-3O2
 
Zang, Klaus D.
- u.a.: Amplification of the MET Gene in Glioma. - In: Genes, Chromosomes &
Cancer. - 12 (1995), 1, S. 63-65
 
- u.a.: Correlation between cytogenetic and clinical findings in 215 human
meningiomas. - In: Acta Neurochirurgica. - Suppl. 65 (1996), S. 73-76
 
- u.a.: DNA amplifications on chromosomes 7, 9 and 12 in glioblastoma
detected by reverse chromosome painting. - In: European Journal of Cancer. -
30A (1994), 8, S. 1124-1127
 
- u.a.: Early Proliferation Enhancement by Monosomy 10 and Intratumoral
Heterogeneity in Malignant Human Gliomas as Revealed by Smear Preparations
From Biopsies. - In: Genes, Chromosomes & Cancer. - 16 (1996), S. 180-184
 
- u.a.: False-positive apoptosis assays due to DNA degradation caused by
routine microwave processing of tissue sections. - In: Medizinische Genetik. -
1 (1996), S. 111-112
 
- u.a.: Frequent Homozygous Loss of p16 and Loss of Heterozygosity of p53 in
Gliomas as Detected by Two-colour In situ Hybridization. - In: Zentralbl
Neurochir. 1996, Suppl, S. 90
 
- u.a.: Genetic heterogeneity of CDKN2 and p53 in human gliomas. - In:
Journal of Neuro-Oncology. - 30 (1996), 2, S. 110
 
- u.a.: Human endogenous retroviral element k10 (HERV-K10): chromosomal
localization by somatic hybrid mapping and fluorescence in situ hybridization.
- In: Cytogenetics and Cell Genetics. - 72 (1996), S. 40-42
 
- u.a.: Isolation and localization of transcribed sequences on human
chromosome 22. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 81-85
 
- u.a.: Isolation of human chromosome 6 specific hncDNA clones from a
somatic hybrid cDNA library. - In: Cytogenetics and Cell Genetics. - 69
(1995), S. 273-278
 
- u.a.: Lack of uniparental isodisomy for chromosome 22 in disomic
meningiomas. - In: Cytogenetics and Cell Genetics. - 71 (1995), S. 139-141
 
- u.a.: Malignant melanoma in a patient with EEC syndrome. - In:
Medizinische Genetik. - 1996 (1996), 1, S. 85
 
- u.a.: Microdissection of Chromosomes - A Rapid Method for the
Identification of Prognostically Relevant Chromosomal Anomalies in Brain
Tumors. - In: Zentralbl Neurochir. 1996, Suppl, S. 93
 
- u.a.: A novel site of DNA amplification on chromosome 1p32-33 in a
rhabdomyosarcoma revealed by comparative genomic hybridization. - In: Human
Genetics. - 97 (1996), S. 87-90
 
- u.a.: Selection towards diploid cells in prostatic carcinoma derived cell
cultures. - In: Prostate 1996, 28, 364-371
 
- u.a.: Partielle Trisomie 1q. - In: Monatsschr. Kinderheilkunde, Suppl. 1. -
144 (1996), 8 (P 518)