delphinidin has been researched along with Abnormalities, Autosome in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (7.14) | 18.7374 |
| 1990's | 9 (64.29) | 18.2507 |
| 2000's | 3 (21.43) | 29.6817 |
| 2010's | 1 (7.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fernando, M; Hammond, D; Reed, M; Salawu, A; Sisley, K; Ul-Hassan, A | 1 |
| Albertson, DG; Alers, JC; Andaya, A; Carroll, P; Collins, C; Fridlyand, J; Jain, AN; Kamkar, S; Kowbel, D; Krijtenburg, PJ; Paris, PL; Pinkel, D; Schröder, FH; Van Dekken, H; Vissers, KJ; Watson, VJ; Wildhagen, MF | 1 |
| Cowles, TA; Elder, FF; Taylor, S | 1 |
| Imamura, Y; Kon, S; Matsuta, M; Sasaki, K | 1 |
| Cremer, T; du Manoir, S; Holtgreve-Grez, H; Lengauer, C; Ried, T; Schoell, B; Schröck, E; Speicher, MR | 1 |
| Micale, MA; Powell, IJ; Sakr, WA; Sanford, JS; Wolman, SR | 1 |
| Borchers, O; Grote, W; Harms, D; Jänig, U; Jenderny, J; Köster, E; Meyer, A | 1 |
| Gejyo, F; Ichikawa, M; Maekawa, H; Mori, M; Noriki, S; Okada, T; Torii, K | 1 |
| Blough, RI; Heerema, NA; Smolarek, TA; Ulbright, TM | 1 |
| Abe, T; Ashihara, T; Hirasawa, Y; Inazawa, J; Kusuzaki, K; Murata, H | 1 |
| Anamthawat-Jónsson, K; Bödvarsdóttir, SK; Eyfjörd, JE; Ogmundsdóttir, H; Sigurdsson, S; Steinarsdóttir, M | 1 |
| Burki, N; Huang, X; Mahoney, MJ; Ozcan, T; Parkash, V; Pejovic, T; Ward, DC | 1 |
| Bell, KA; du Manoir, S; Feinberg, RF; Haddad, BR; Van Deerlin, PG | 1 |
| Cremer, T; Emmerich, P; Hofmann, MC; Jauch, A; Walt, H | 1 |
1 trial(s) available for delphinidin and Abnormalities, Autosome
| Article | Year |
|---|---|
[Detection of numerical chromosomal aberrations in hematopoietic malignancy by in situ hybridization on bone marrow aspirate paraffin sections].
Topics: Bone Marrow Cells; Chromosome Aberrations; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 8; Hematologic Diseases; Humans; In Situ Hybridization; Karyotyping; Microtomy; Paraffin | 1996 |
13 other study(ies) available for delphinidin and Abnormalities, Autosome
| Article | Year |
|---|---|
High quality genomic copy number data from archival formalin-fixed paraffin-embedded leiomyosarcoma: optimisation of universal linkage system labelling.
Topics: Algorithms; Chromosome Aberrations; Chromosome Mapping; Comparative Genomic Hybridization; DNA; Electrophoresis, Agar Gel; Female; Gene Dosage; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Genetic Techniques; Humans; In Situ Hybridization, Fluorescence; Leiomyosarcoma; Models, Genetic; Paraffin; Reproducibility of Results; Retrospective Studies; Specimen Handling | 2012 |
High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays.
Topics: Chromosome Aberrations; Chromosome Mapping; Formaldehyde; Histological Techniques; Humans; Male; Neoplasm Metastasis; Nucleic Acid Hybridization; Oligonucleotide Array Sequence Analysis; Paraffin; Prostatic Neoplasms; Sensitivity and Specificity; Treatment Outcome | 2003 |
Identification of abnormal chromosomal complement in formalin-fixed, paraffin-embedded placental tissue.
Topics: Chromosome Aberrations; DNA Probes; Female; Fixatives; Formaldehyde; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Paraffin; Placenta; Pregnancy; Prenatal Diagnosis; Tissue Embedding | 1995 |
Applications of DNA flow cytometry and fluorescence in situ hybridization using a chromosome-specific DNA probe on paraffin-embedded tissue sections of primary malignant melanomas.
Topics: Adult; Aged; Aged, 80 and over; Chromosome Aberrations; Chromosomes, Human, Pair 17; DNA Probes; DNA, Neoplasm; Female; Flow Cytometry; Humans; In Situ Hybridization; Male; Melanoma; Middle Aged; Paraffin; Ploidies; Skin Neoplasms; Tissue Fixation | 1994 |
Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification.
Topics: Base Sequence; Chromosome Aberrations; Chromosome Mapping; DNA Primers; DNA, Neoplasm; Fluorescein-5-isothiocyanate; Formaldehyde; Genome, Human; Histological Techniques; Humans; Karyotyping; Molecular Sequence Data; Neoplasms; Nucleic Acid Hybridization; Paraffin; Polymerase Chain Reaction | 1993 |
Defining the extent and nature of cytogenetic events in prostatic adenocarcinoma: paraffin FISH vs. metaphase analysis.
Topics: Adenocarcinoma; Chromosome Aberrations; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 7; Chromosomes, Human, Pair 8; Cytogenetics; Humans; In Situ Hybridization, Fluorescence; Male; Metaphase; Paraffin; Prostatic Neoplasms; Y Chromosome | 1993 |
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 12; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 8; DNA Probes; Endodermal Sinus Tumor; Female; Histological Techniques; Humans; In Situ Hybridization; Male; Ovarian Neoplasms; Paraffin; Retrospective Studies; Sex Chromosome Aberrations; Testicular Neoplasms; X Chromosome; Y Chromosome | 1995 |
Bicolor fluorescence in situ hybridization on nuclei from formalin-fixed, paraffin-embedded testicular germ cell tumors: comparison with standard metaphase analysis.
Topics: Cell Nucleus; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 12; DNA, Neoplasm; Fixatives; Formaldehyde; Humans; In Situ Hybridization, Fluorescence; Interphase; Karyotyping; Neoplasms, Germ Cell and Embryonal; Paraffin | 1997 |
Ploidy analysis in paraffin-embedded malignant fibrous histiocytoma by DNA cytofluorometry and flourescence in situ hybridization.
Topics: Biopsy; Centromere; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 8; DNA Probes; DNA, Neoplasm; Flow Cytometry; Genetic Markers; Histiocytoma, Benign Fibrous; Humans; In Situ Hybridization, Fluorescence; Paraffin; Ploidies | 1997 |
Simultaneous detection of p53 nuclear protein and chromosome aberrations on sections from formalin-fixed, paraffin-embedded breast cancer tissue.
Topics: Breast Neoplasms; Chromosome Aberrations; Chromosomes, Human, Pair 17; Female; Formaldehyde; Humans; In Situ Hybridization, Fluorescence; Paraffin; Tissue Fixation; Tumor Suppressor Protein p53 | 1998 |
Cytogenetical diagnosis in paraffin-embedded fetoplacental tissue using comparative genomic hybridization.
Topics: Chromosome Aberrations; Chromosomes, Human, Pair 13; Chromosomes, Human, Pair 18; Chromosomes, Human, Pair 2; Chromosomes, Human, Pair 21; Chromosomes, Human, Pair 6; Cytogenetic Analysis; Down Syndrome; Female; Gene Deletion; Humans; Isochromosomes; Karyotyping; Nucleic Acid Hybridization; Paraffin; Placenta; Pregnancy; Tissue Embedding; Trisomy | 2000 |
Diagnosis of aneuploidy in archival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization.
Topics: Abortion, Spontaneous; Aneuploidy; Archives; Chromosome Aberrations; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 22; Cytogenetic Analysis; DNA; Down Syndrome; Female; Fluorescent Dyes; Humans; Nucleic Acid Hybridization; Paraffin; Polymerase Chain Reaction; Pregnancy; Retrospective Studies; Tissue Embedding; Trisomy; X Chromosome | 2001 |
Interphase cytogenetics in paraffin embedded sections from human testicular germ cell tumor xenografts and in corresponding cultured cells.
Topics: Animals; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 1; DNA Probes; Humans; Interphase; Male; Metaphase; Mice; Mice, Nude; Neoplasm Transplantation; Nucleic Acid Hybridization; Paraffin; Ploidies; Teratoma; Testicular Neoplasms; Tumor Cells, Cultured | 1989 |