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1. Full Text Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study
by Dehghan, Abbas, MD and Köttgen, Anna, MD and Yang, Qiong, PhD and Hwang, Shih-Jen, PhD and Kao, WH Linda, PhD and Rivadeneira, Fernando, MD and Boerwinkle, Eric, PhD and Levy, Daniel, MD and Hofman, Albert, MD and Astor, Brad C, PhD and Benjamin, Emelia J, MD and van Duijn, Cornelia M, PhD and Witteman, Jacqueline C, PhD and Coresh, Josef, MD and Fox, Caroline S, Dr
The Lancet, ISSN 0140-6736, 2008, Volume 372, Issue 9654, pp. 1953 - 1961
Summary Background Hyperuricaemia, a highly heritable trait, is a key risk factor for gout. We aimed to identify novel genes associated with serum uric acid... 
Internal Medicine | UNITED-STATES | FRAMINGHAM | MEDICINE, GENERAL & INTERNAL | HEART-DISEASE | SERUM URATE | DESIGN | HYPERURICEMIA | UNIFIED APPROACH | APICAL MEMBRANE | PRACTICE RESEARCH DATABASE | ATHEROSCLEROSIS RISK | Genetics, Population | Genome-Wide Association Study | Prevalence | Chromosomes, Human, 6-12 and X - genetics | Humans | Middle Aged | Risk Factors | Genotype | Male | Hyperuricemia - metabolism | Genome, Human - genetics | Gout - etiology | Hyperuricemia - genetics | Netherlands | Gout - epidemiology | Alleles | Polymorphism, Single Nucleotide - genetics | Chromosomes, Human, 4-5 - genetics | Female | Gout - genetics | Uric Acid - blood | Hyperuricemia - complications | Cohort Studies | Studies | Sample size | Genetic research | Eye diseases | Risk factors | Medical ethics | Family physicians | Chronic illnesses | epidemiology | genome-wide association | uric acid | gout
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2. Full Text The prognostic value of Ki-67, p53, epidermal growth factor receptor, 1p36, 9p21, 10q23, and 17p13 in skull base chordomas
by Horbinski, Craig and Oakley, Gerard J and Cieply, Kathleen and Mantha, Geeta S and Nikiforova, Marina N and Dacic, Sanja and Seethala, Raja R
Archives of Pathology and Laboratory Medicine, ISSN 0003-9985, 08/2010, Volume 134, Issue 8, pp. 1170 - 1176
Context.-Skull base chordomas are rare, locally aggressive, notochord-derived neoplasms for which prognostically relevant biomarkers are not well established.... 
MEDICINE, RESEARCH & EXPERIMENTAL | MANAGEMENT | TUMOR | PROLIFERATION | PATHOLOGY | LOCUS | FEATURES | DELETION | IMMUNOHISTOCHEMICAL ANALYSIS | MEDICAL LABORATORY TECHNOLOGY | COMPARATIVE GENOMIC HYBRIDIZATION | EXPRESSION | FAMILIAL CHORDOMA | Cell Proliferation | Prognosis | Chromosomes, Human, 6-12 and X - genetics | Humans | Middle Aged | Chordoma - metabolism | Ki-67 Antigen - metabolism | Male | Loss of Heterozygosity | Skull Base Neoplasms - mortality | Chromosomes, Human, Pair 17 - genetics | Young Adult | Receptor, Epidermal Growth Factor - metabolism | Skull Base Neoplasms - genetics | Biomarkers, Tumor - metabolism | Adult | Female | Retrospective Studies | Chromosomes, Human, Pair 1 - genetics | Child | Pennsylvania - epidemiology | Chordoma - genetics | Tumor Suppressor Protein p53 - metabolism | Survival Rate | Skull Base Neoplasms - diagnosis | Adolescent | Aged | Chordoma - mortality | Chordoma - diagnosis | Skull Base Neoplasms - metabolism | Fluorescence | Epidermal growth factor | Tumor proteins | Tumors
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3. Full Text Relaxin receptors 1 and 2 and nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) mRNAs are expressed in oral components of developing mice
by Duarte, Carolina and Kobayashi, Yukiho and Kawamoto, Tatsuo and Moriyama, Keiji
Archives of Oral Biology, ISSN 0003-9969, 2013, Volume 59, Issue 2, pp. 111 - 118
Abstract Objective Relaxin is a pleiotropic hormone of the insulin-like peptide hormone family that plays an important role in reproductive physiology as well... 
Advanced Basic Science | Dentistry | Craniofacial development | Relaxin receptors | Gene expression | Relaxin | FIBROBLASTS | CARTILAGE | MATRIX METALLOPROTEINASES | OSTEOPROTEGERIN OPG | SKELETAL-MUSCLE | MORPHOGENESIS | FAMILY PEPTIDES | ACTIVATOR | DENTISTRY, ORAL SURGERY & MEDICINE | DIFFERENTIATION | LIGAND RANKL | Cartilage - embryology | Chromosomes, Human, 6-12 and X - genetics | Humans | Mice, Inbred C57BL | RNA, Messenger - genetics | Facial Bones - embryology | Animals | In Situ Hybridization | Embryo, Mammalian - cytology | Tooth - embryology | Receptors, Glucocorticoid - genetics | Mice | Receptors, G-Protein-Coupled - genetics | Tongue - embryology | Corticosteroids | Messenger RNA | Chorionic gonadotropin | Peptides | Genomics | College graduates | Physiological aspects | Steroids
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4. Full Text HPV type-related chromosomal profiles in high-grade cervical intraepithelial neoplasia
by Bierkens, M and Wilting, S.M and van Wieringen, W.N and van de Wiel, M and Ylstra, B and Meijer, C.J.L.M and Snijders, P.J.F and Steenbergen, R.D.M
BMC Cancer, ISSN 1471-2407, 2012, Volume 12, Issue 1, pp. 36 - 36
Background: The development of cervical cancer and its high-grade precursor lesions (Cervical Intraepithelial Neoplasia grade 2/3 [CIN2/3]) result from a... 
High-grade cervical intraepithelial neoplasia | Chromosomal aberrations | Array CGH | Cervical cancer | HPV | P16(INK4A) EXPRESSION | HLA CLASS-I | PROMOTER METHYLATION | MALIGNANT LESIONS | COMPARATIVE-GENOMIC-HYBRIDIZATION | MHC CLASS-I | UTERINE CERVIX | HUMAN-PAPILLOMAVIRUS GENOTYPES | ONCOLOGY | RECURRENT PATTERN | SQUAMOUS-CELL CARCINOMAS | Species Specificity | Chromosomes, Human, 6-12 and X - genetics | Humans | Middle Aged | Alphapapillomavirus - classification | Uterine Cervical Neoplasms - genetics | Chromosomes, Human, Pair 17 - genetics | Cervical Intraepithelial Neoplasia - virology | Papillomavirus Infections - genetics | Chromosomes, Human, 1-3 - genetics | Chromosome Aberrations | Uterine Cervical Neoplasms - virology | Adult | Chromosomes, Human, 4-5 - genetics | Female | Papillomavirus Infections - virology | Cervical Intraepithelial Neoplasia - genetics | Cluster Analysis | Complications and side effects | Cervix dysplasia | Chromosome abnormalities | Genetic aspects | Research | Papillomavirus infections | Risk factors
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5. Full Text Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types
by Virmani, Arvind K and Fong, Kwun M and Kodagoda, Dulmini and McIntire, Donald and Hung, Jaclyn and Tonk, Vijay and Minna, John D and Gazdar, Adi F
Genes, Chromosomes and Cancer, ISSN 1045-2257, 04/1998, Volume 21, Issue 4, pp. 308 - 319
Allelic loss is a hallmark of tumor suppressor gene (TSG) inactivation. We have allelotyped 29 paired lymphoblastoid and lung cancer cell lines derived from 11... 
ALLELIC LOSSES | HOMOZYGOUS DELETION | DINUCLEOTIDE REPEAT | P53 GENE | ONCOLOGY | BREAST CARCINOMAS | GENETICS & HEREDITY | TUMOR-SUPPRESSOR GENE | SQUAMOUS-CELL CARCINOMA | OVARIAN-CANCER | FREQUENT LOSS | IN-SITU | Chromosome Deletion | Lung Neoplasms - genetics | Chromosomes, Human, 21-22 and Y - genetics | Chromosomes, Human, 6-12 and X - genetics | Humans | Middle Aged | Chromosomes, Human, 19-20 - genetics | Genotype | Male | Loss of Heterozygosity - genetics | Chromosomes, Human, 1-3 - genetics | Alleles | Aged, 80 and over | Adult | Chromosomes, Human, 4-5 - genetics | Female | Aged | Tumor Cells, Cultured | Chromosomes, Human, 13-15 - genetics
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6. Full Text OWEN: Aligning long collinear regions of genomes
by Ogurtsov, Aleksey Y and Roytberg, Mikhail A and Shabalina, Svetlana A and Kondrashov, Alexey S
Bioinformatics, ISSN 1367-4803, 12/2002, Volume 18, Issue 12, pp. 1703 - 1704
OWEN is an interactive tool for aligning two long DNA sequences that represents similarity between them by a chain of collinear local similarities. OWEN... 
STATISTICS & PROBABILITY | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | MATHEMATICS, INTERDISCIPLINARY APPLICATIONS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BIOCHEMICAL RESEARCH METHODS | Conserved Sequence - genetics | Information Storage and Retrieval - methods | Chromosomes, Human, 6-12 and X - genetics | Humans | Molecular Sequence Data | Sequence Homology, Nucleic Acid | Sequence Alignment - methods | Algorithms | Base Sequence | Software | Genome | Databases, Nucleic Acid | Sequence Analysis, DNA - methods | Evolution, Molecular
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7. Full Text Chromosome 6 Abnormality with Associated Dysmorphological Features and Erythrokeratoderma
by LEGLER, ALLISON A
Pediatric Dermatology, ISSN 0736-8046, 07/2008, Volume 25, Issue 4, pp. 503 - 504
Letters to the Editor are welcomed for publication (subject to editing). Letters must be signed by all authors, typewritten double spaced, and must not exceed... 
PEDIATRICS | DERMATOLOGY | Gene Duplication | Malignant Atrophic Papulosis - genetics | Chromosomes, Human, 6-12 and X - genetics | Humans | Child, Preschool | Male | Abnormalities, Multiple - genetics
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8. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation
by Cetin, Z and Mihci, E and Keser, I and Karaali, K and Berker, S and Lüleci, Güven
Genetic Counseling, ISSN 1015-8146, 2012, Volume 23, Issue 2, pp. 239 - 247
Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2)... 
Trisomy 6p23→pter | Complex chromosomal rearrangement | 4:2 Segregation | Trisomy 9pter→q21.2 | MEDICINE, RESEARCH & EXPERIMENTAL | DIAGNOSIS | 4:2 segregation | Trisomy 9pter -> q21.2 | IN-SITU HYBRIDIZATION | MEDICAL ETHICS | Trisomy 6p23 -> pter | CHILD | BREAKPOINTS | ORIGIN | FLUORESCENCE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | CHROMOSOMAL REARRANGEMENT | PATIENT | ABERRATIONS | Translocation, Genetic | Trisomy - genetics | Chromosomes, Human, 6-12 and X - genetics | Abnormalities, Multiple - diagnosis | Humans | Karyotyping | Chromosome Aberrations | In Situ Hybridization, Fluorescence | Male | Abnormalities, Multiple - genetics | Infant, Newborn | Karyotype
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9. Full Text Renal Metanephric Adenoma With Previously Unreported Cytogenetic Abnormalities: Case Report and Review of the Literature
by Rakheja, Dinesh and Lian, Fangru and Tomlinson, Gail E and Ewalt, David H and Schultz, Roger A and Margraf, Linda R
Pediatric and Developmental Pathology, ISSN 1093-5266, 4/2005, Volume 8, Issue 2, pp. 218 - 223
We report a case of a renal metanephric adenoma in a 10-year-old boy, in which cytogenetic analysis showed a balanced translocation, t(9;15)(p24;q24) and a... 
Pathology | metanephric adenoma | papillary renal cell carcinoma | Medicine & Public Health | cytogenetics | Wilms tumor | Cytogenetics | Papillary renal cell carcinoma | Metanephric adenoma | CHROMOSOME-17 GAIN | PATHOLOGY | PAPILLARY CARCINOMA | CELL CARCINOMA | WILMS-TUMOR | GENE | TUMOR-SUPPRESSOR | PEDIATRICS | KIDNEY | Kidney Neoplasms - genetics | Chromosome Banding | Adenoma - genetics | Chromosomes, Human, 6-12 and X - genetics | Humans | Male | Kidney Neoplasms - metabolism | Chromosomes, Human, Pair 9 | Chromosomes, Human, Pair 15 - genetics | Adenoma - metabolism | Adenoma - pathology | Biomarkers, Tumor - metabolism | Kidney Neoplasms - pathology | Chromosomes, Human, Pair 12 | Child | Chromosome Inversion - genetics | Translocation, Genetic - genetics | Adenoma | Carcinoma, Renal cell | Tumors
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10. Full Text Molecular analysis of genetic changes in ependymomas
by Bijlsma, E. K and Voesten, A. M and Bijleveld, E. H and Troost, D and Westerveld, A and Mérel, P and Thomas, G and Hulsebos, T. J
Genes, chromosomes & cancer, ISSN 1045-2257, 1995, Volume 13, Issue 4, pp. 272 - 277
Ependymomas are glial cell-derived tumors. They are, in contrast to other gliomas (astrocytomas, oligodendrogliomas, and oligoastrocytomas), ill-defined with... 
HUMAN BRAIN-TUMORS | ONCOLOGY | ABNORMALITIES | ASTROCYTOMAS | GENETICS & HEREDITY | HUMAN GLIOMAS | CHROMOSOME-22 | MUTATIONS | DELETIONS | HETEROZYGOSITY | TUMORIGENESIS | Chromosome Deletion | Chromosomes, Human, 6-12 and X - genetics | Chromosomes, Human - genetics | Humans | Middle Aged | Brain Neoplasms - genetics | Child, Preschool | Infant | Male | Genetic Markers | Ependymoma - genetics | Chromosomes, Human, Pair 19 | Chromosomes, Human, Pair 17 | Adolescent | Alleles | Chromosomes, Human, Pair 13 | Adult | Female | Aged | Chromosomes, Human, Pair 22 | Child
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11. Full Text Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14
by Pedeutour, F and Quade, BJ and Sornberger, K and Tallini, G and Ligon, AH and Weremowicz, S and Morton, CC
GENES CHROMOSOMES & CANCER, ISSN 1045-2257, 02/2000, Volume 27, Issue 2, pp. 209 - 215
Uterine lipoleiomyomas are extremely rare tumors consisting of a mixture of mature adipocytes and smooth muscle cells. Using G-banding and FISH, we... 
ARCHITECTURAL FACTOR | GENE | LIPOMAS | ONCOLOGY | GENETICS & HEREDITY | LEIOMYOMATA | PHENOTYPE | EXPRESSION | TUMORS | Immunohistochemistry | Uterine Neoplasms - genetics | Translocation, Genetic | Uterine Neoplasms - metabolism | Chromosomes, Human, 6-12 and X - genetics | Uterine Neoplasms - pathology | High Mobility Group Proteins - analysis | Humans | Lipoma - genetics | In Situ Hybridization, Fluorescence | Leiomyoma - metabolism | Lipoma - pathology | Leiomyoma - pathology | Karyotyping | Female | Lipoma - metabolism | Aged | HMGA2 Protein | Chromosomes, Human, Pair 14 - genetics | Leiomyoma - genetics
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12. Full Text USCAP Specialty Conference: Case 4
by Parham, David and Parham, David
Pediatric and Developmental Pathology, ISSN 1093-5266, 2/2005, Volume 8, Issue 1, pp. 85 - 87
Medicine & Public Health | Pathology | CHROMOSOME-ABERRATIONS | PEDIATRICS | BONE | PATHOLOGY | FIBROUS DYSPLASIA | OSTEOFIBROUS DYSPLASIA | ADAMANTINOMA | LESIONS | Ameloblastoma - diagnosis | Fibroma, Ossifying - genetics | Translocation, Genetic | Diagnosis, Differential | Chromosomes, Human, 6-12 and X - genetics | Humans | Fibroma, Ossifying - pathology | Chromosomes, Human, Pair 21 - genetics | Osteosarcoma - diagnosis | Bone Neoplasms - pathology | Fibrous Dysplasia of Bone - diagnosis | Osteoblasts - pathology | Female | Bone Neoplasms - genetics | Child | Case studies | Development and progression | Diagnosis | Fibromas
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13. Fluorescence in situ hybridization to assess transitional changes of aneuploidy for chromosomes 7, 8, 10, 12, 16, X and Y in metastatic prostate cancer following anti-androgen therapy
by Kasahara, K and Taguchi, T and Yamasaki, I and Karashima, T and Kamada, M and Yuri, K and Shuin, T
International journal of oncology, ISSN 1019-6439, 2001, Volume 19, Issue 3, pp. 543 - 549
There have been few detailed studies conducted on the cell population in relation to cytogenetic changes between the pre- and post-treatment periods in... 
fluorescence in situ hybridization | prostate cancer | ONCOLOGY | ADENOCARCINOMA | chromosome | DNA PROBES | DISEASE | CARCINOMAS | COMPARATIVE GENOMIC HYBRIDIZATION | CYTOGENETIC ANALYSIS | GENETIC ALTERATIONS | Prostate-Specific Antigen | Prostatic Hyperplasia - pathology | Chromosomes, Human, 6-12 and X - genetics | Humans | Middle Aged | Bone Neoplasms - secondary | Aneuploidy | Male | Chromosome Disorders | Y Chromosome - genetics | Prostatic Neoplasms - genetics | Sex Chromosomes - genetics | Adenocarcinoma - genetics | Bone Neoplasms - genetics | Bone Neoplasms - drug therapy | Prostatic Hyperplasia - drug therapy | X Chromosome - genetics | Prostatic Neoplasms - drug therapy | Chromosomes, Human, Pair 16 - genetics | Prostatic Neoplasms - pathology | Chromosomes, Human - genetics | In Situ Hybridization, Fluorescence | Adenocarcinoma - drug therapy | Prostatic Hyperplasia - genetics | Adenocarcinoma - secondary | Chromosome Aberrations - genetics | Androgen Antagonists - therapeutic use | Aged
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14. Malignant glioma: The involvement of loss of allelic heterozygosity and PTEN mutations in a group of Malay patients
by Zainuddin, N and Jaafar, H and Isa, M.N and Abdullah, J.M
Southeast Asian Journal of Tropical Medicine and Public Health, ISSN 0125-1562, 05/2005, Volume 36, Issue 3, pp. 748 - 756
Frequent loss of heterozygosity (LOH) and mutations of the tumor suppressor gene PTEN (phosphatase and tensin homologue deleted from chromosome 10) have been... 
PTEN Phosphohydrolase - genetics | Age Distribution | Chromosomes, Human, 6-12 and X - genetics | Humans | Middle Aged | Child, Preschool | Male | Glioma - epidemiology | Mutation - genetics | Incidence | Loss of Heterozygosity - genetics | Glioma - genetics | Adolescent | Alleles | Malaysia - epidemiology | Polymerase Chain Reaction | Sex Distribution | Adult | Female | Child | Genes, Tumor Suppressor
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15. Assessment of genomic imbalances in malignant fibrous histiocytomas by comparative genomic hybridization
by Hinze, Raoul and Schagdarsurengin, Undraga and Taubert, Helge and Meye, Axel and Würl, Peter and Holzhausen, Hans-Jürgen and Rath, Friedrich-Wilhelm and Schmidt, Hannelore
International Journal of Molecular Medicine, ISSN 1107-3756, 1999, Volume 3, Issue 1, pp. 75 - 79
In order to investigate genomic imbalances, comparative genomic hybridization was applied to 20 malignant fibrous histiocytomas. Deletions were rare and found... 
Cytogenetics | Amplification 12q13-15 | Malignant fibrous histiocytoma | CGH | malignant fibrous histiocytoma | MEDICINE, RESEARCH & EXPERIMENTAL | LOSSES | SOFT-TISSUE SARCOMAS | cytogenetics | IDENTIFICATION | TUMORS | amplification 12q13-15 | 19P+ MARKER CHROMOSOME | AMPLIFICATION | GAINS | GENE | MDM2 | REVEALS | Histiocytoma, Benign Fibrous - genetics | Chromosomes, Human, 16-18 - genetics | Chromosomes, Human, 6-12 and X - genetics | Humans | Chromosomes, Human, 19-20 - genetics | Aneuploidy | Male | Chromosomes, Human, 1-3 - genetics | Chromosome Aberrations | Histiocytoma, Benign Fibrous - pathology | Chromosomes, Human, 4-5 - genetics | Female | Chromosomes, Human, 13-15 - genetics | In Situ Hybridization - methods
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16. Proliferative activity and chromosomal alterations of smooth muscle cells in atherosclerosis
by Alonso, GF and Grana, DR and Turconi, P and Colombo, B and Lavezzi, AM and Milei, J and Matturri, L
MEDICINA-BUENOS AIRES, ISSN 0025-7680, 2000, Volume 60, Issue 5, pp. 595 - 601
Atherosclerosis is the most frequent cause of death in industrialized countries. Lesions are characterized by lipid deposits, focal thickening of the arterial... 
atherosclerosis | VIVO | CORONARY | MACROPHAGES | atherosclerotic plaque | PLAQUE | LESIONS | smooth muscle cells | MEDICINE, GENERAL & INTERNAL | IN-VITRO | GROWTH-FACTORS | ACCUMULATION | chromosomal alterations | Trisomy | Chromosomes, Human, 6-12 and X - genetics | Humans | Fibroblast Growth Factors - genetics | In Situ Hybridization, Fluorescence | Proto-Oncogene Proteins - genetics | Arteriosclerosis - genetics | Tumor Suppressor Protein p53 - genetics | Fibroblast Growth Factor 3 | Chromosomes, Human, Pair 11 - metabolism | Chromosomes, Human, Pair 7 - genetics | Nuclear Proteins - genetics | Arteriosclerosis - pathology | Muscle, Smooth - pathology
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17. Translocation (3;12) (p21-pter; q24.1-qter) and phenylketonuria
by Ganguly, BB and Dalvi, R and Mehta, AV
CYTOBIOS, ISSN 0011-4529, 2001, Volume 106, Issue 411, pp. 63 - 70
Cytogenetic karyotyping in mental retardation associated with physical dysmorphism has been regarded as the primary key for the classification of syndromes and... 
CELL LUNG-CANCER | GROWTH FACTOR-I | mental retardation | GENES | translocation (3;12) | phenylketonuria | SISTER-CHROMATID EXCHANGES | LYMPHOCYTES | AGE | CELL BIOLOGY | Chromosome Banding | Phenylketonurias - genetics | Chromosomes, Human, 6-12 and X - genetics | Humans | Intellectual Disability - genetics | Phenotype | Pedigree | Chromosomes, Human, 1-3 - genetics | Karyotyping | Female | Child | Abnormalities, Multiple - genetics | Translocation, Genetic - genetics
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18. Full Text Systematic search for uniparental disomy in early fetal losses: The results and a review of the literature
by Shaffer, Lisa G and McCaskill, Christopher and Adkins, Kenneth and Hassold, Terry J
American Journal of Medical Genetics, ISSN 0148-7299, 10/1998, Volume 79, Issue 5, pp. 366 - 372
About 20% of all human conceptuses are estimated to be trisomic and trisomy of all chromosomes remains a common cause of early fetal loss. Uniparental disomy... 
molecular polymorphism | genomic imprinting | confined placental mosaicism | embryonic lethality | chromosomal mosaicism | Molecular polymorphism | Confined placental mosaicism | Chromosomal mosaicism | Embryonic lethality | Genomic imprinting | SILVER-RUSSELL-SYNDROME | MATERNAL HETERODISOMY | ANGELMAN-SYNDROME | BECKWITH-WIEDEMANN SYNDROME | INTRAUTERINE GROWTH-RETARDATION | PRADER-WILLI SYNDROME | CONGENITAL HEART-DISEASE | GENETICS & HEREDITY | PATERNAL ISODISOMY | EUPLOID CELL-LINE | Chromosomes, Human, 16-18 - genetics | Chromosomes, Human, 21-22 and Y - genetics | Chromosomes, Human, 6-12 and X - genetics | Chromosomes, Human - genetics | Humans | Chromosomes, Human, 19-20 - genetics | Male | Genetic Markers | Genomic Imprinting - genetics | Karyotyping - methods | Pregnancy | Trisomy - genetics | Fetal Death | Chromosomes, Human, 1-3 - genetics | Chromosomes, Human, 4-5 - genetics | Female | Mosaicism | Polymorphism, Genetic - genetics | Chromosomes, Human, 13-15 - genetics | X Chromosome - genetics
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