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Results: 1-25 | 26-27
Results: 1-25/27
Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL)
Authors: Brown, J Saracoglu, K Uhrig, S Speicher, MR Eils, R Kearney, L
Citation: J. Brown et al., Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL), NAT MED, 7(4), 2001, pp. 497-501
Karyotyping mouse chromosomes by multiplex-FISH (M-FISH)
Authors: Jentsch, I Adler, ID Carter, NP Speicher, MR
Citation: I. Jentsch et al., Karyotyping mouse chromosomes by multiplex-FISH (M-FISH), CHROMOS RES, 9(3), 2001, pp. 211-214
AcroM fluorescent in situ hybridization analyses of marker chromosomes
Authors: Langer, S Fauth, C Rocchi, M Murken, J Speicher, MR
Citation: S. Langer et al., AcroM fluorescent in situ hybridization analyses of marker chromosomes, HUM GENET, 109(2), 2001, pp. 152-158
Classifying by colors: FISH-based genome analysis
Authors: Fauth, C Speicher, MR
Citation: C. Fauth et Mr. Speicher, Classifying by colors: FISH-based genome analysis, CYTOG C GEN, 93(1-2), 2001, pp. 1-10
Facilitating haplotype analysis by fully automated analysis of all chromosomes in human-mouse hybrid cell lines
Authors: Langer, S Jentsch, I Gangnus, R Yan, H Lengauer, C Speicher, MR
Citation: S. Langer et al., Facilitating haplotype analysis by fully automated analysis of all chromosomes in human-mouse hybrid cell lines, CYTOG C GEN, 93(1-2), 2001, pp. 11-15
cDNA cloning, chromosome assignment, and genomic structure of a human geneencoding a novel member of the RBM family
Authors: Stover, C Gradl, G Jentsch, I Speicher, MR Wieser, R Schwaeble, W
Citation: C. Stover et al., cDNA cloning, chromosome assignment, and genomic structure of a human geneencoding a novel member of the RBM family, CYTOG C GEN, 92(3-4), 2001, pp. 225-230
New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization
Authors: Saracoglu, K Brown, J Kearney, L Uhrig, S Azofeifa, J Fauth, C Speicher, MR Eils, R
Citation: K. Saracoglu et al., New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization, CYTOMETRY, 44(1), 2001, pp. 7-15
Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin
Authors: Fauth, C Bartels, I Haaf, T Speicher, MR
Citation: C. Fauth et al., Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin, AM J MED G, 103(2), 2001, pp. 160-162
Securin is required for chromosomal stability in human cells
Authors: Jallepalli, PV Waizenegger, IC Bunz, F Langer, S Speicher, MR Peters, JM Kinzler, KW Vogelstein, B Lengauer, C
Citation: Pv. Jallepalli et al., Securin is required for chromosomal stability in human cells, CELL, 105(4), 2001, pp. 445-457
Carcinogen-specific induction of genetic instability
Authors: Bardelli, A Cahill, CP Lederer, G Speicher, MR Kinzler, KW Vogelstein, B Lengauer, C
Citation: A. Bardelli et al., Carcinogen-specific induction of genetic instability, P NAS US, 98(10), 2001, pp. 5770-5775
Assignment of CD163B, the gene encoding M160, a novel scavenger receptor, to human chromosome 12p13.3 by in situ hybridization and somatic cell hybrid analysis
Authors: Stover, CM Schleypen, J Gronlund, J Speicher, MR Schwaeble, WJ Holmskov, U
Citation: Cm. Stover et al., Assignment of CD163B, the gene encoding M160, a novel scavenger receptor, to human chromosome 12p13.3 by in situ hybridization and somatic cell hybrid analysis, CYTOG C GEN, 90(3-4), 2000, pp. 246-247
Classification accuracy in multiple color fluorescence imaging microscopy
Authors: Castleman, KR Eils, R Morrison, L Piper, J Saracoglu, K Schulze, MA Speicher, MR
Citation: Kr. Castleman et al., Classification accuracy in multiple color fluorescence imaging microscopy, CYTOMETRY, 41(2), 2000, pp. 139-147
Breakpoint within the nucleolus organizer region resulting in a reciprocaltranslocation t(4;14)(q21;p12)
Authors: Grabowski, M Fauth, C Wirtz, A Speicher, MR
Citation: M. Grabowski et al., Breakpoint within the nucleolus organizer region resulting in a reciprocaltranslocation t(4;14)(q21;p12), AM J MED G, 92(4), 2000, pp. 264-268
Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative hybridization and multicolor bar coding (vol 80, pg 1031, 2000)
Authors: Speicher, MR Petersen, S Uhrig, S Jentsch, I Fauth, C Eils, R Petersen, I
Citation: Mr. Speicher et al., Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative hybridization and multicolor bar coding (vol 80, pg 1031, 2000), LAB INV, 80(8), 2000, pp. 1145-1145
Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding
Authors: Speicher, MR Petersen, S Uhrig, S Jentsch, I Fauth, C Eils, R Petersen, I
Citation: Mr. Speicher et al., Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding, LAB INV, 80(7), 2000, pp. 1031-1041
Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito andasymmetry
Authors: Schmidt, H Uhrig, S Lederer, G Murken, J Speicher, MR Schuffenhauer, S
Citation: H. Schmidt et al., Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito andasymmetry, J MED GENET, 37(10), 2000, pp. 804-806
Risk estimates for carriers of chromosome reciprocal translocation t(4;9)(p15.2;p13)
Authors: Midro, AT Panasiuk, B Stasiewicz-Jarocka, B Iwanowski, PS Fauth, C Speicher, MR Lesniewicz, R
Citation: At. Midro et al., Risk estimates for carriers of chromosome reciprocal translocation t(4;9)(p15.2;p13), CLIN GENET, 58(2), 2000, pp. 153-155
Malignant potential and cytogenetic characteristics of occult disseminatedtumor cells in esophageal cancer
Authors: Hosch, S Kraus, J Scheunemann, P Izbicki, JR Schneider, C Schumacher, U Witter, K Speicher, MR Pantel, K
Citation: S. Hosch et al., Malignant potential and cytogenetic characteristics of occult disseminatedtumor cells in esophageal cancer, CANCER RES, 60(24), 2000, pp. 6836-6840
An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH
Authors: Azofeifa, J Fauth, C Kraus, J Maierhofer, C Langer, S Bolzer, A Reichman, J Schuffenhauer, S Speicher, MR
Citation: J. Azofeifa et al., An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH, AM J HU GEN, 66(5), 2000, pp. 1684-1688
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)
Authors: Holinski-Feder, E Reyniers, E Uhrig, S Golla, A Wauters, J Kroisel, P Bossuyt, P Rost, I Jedele, K Zierler, H Schwab, S Wildenauer, D Speicher, MR Willems, PJ Meitinger, T Kooy, RF
Citation: E. Holinski-feder et al., Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3), AM J HU GEN, 66(1), 2000, pp. 16-25
Biological relevance of occult tumor cells in a lymph node of a patient with resectable esophageal cancer
Authors: Scheunemann, P Hosch, SB Witter, K Kraus, J Speicher, MR Pantel, K Izbicki, JR
Citation: P. Scheunemann et al., Biological relevance of occult tumor cells in a lymph node of a patient with resectable esophageal cancer, LANG ARCH S, 1999, pp. 105-108
Assignment of the gene encoding mannan-binding lectin-associated serine protease 2 (MASP2) to human chromosome 1p36.3 -> p36.2 by in situ hybridization and somatic cell hybrid analysis
Authors: Stover, CM Schwaeble, WJ Lynch, NJ Thiel, S Speicher, MR
Citation: Cm. Stover et al., Assignment of the gene encoding mannan-binding lectin-associated serine protease 2 (MASP2) to human chromosome 1p36.3 -> p36.2 by in situ hybridization and somatic cell hybrid analysis, CYTOG C GEN, 84(3-4), 1999, pp. 148-149
A complete set of repeat-depleted, PCR-amplifiable, human chromosome-specific painting probes
Authors: Bolzer, A Craig, JM Cremer, T Speicher, MR
Citation: A. Bolzer et al., A complete set of repeat-depleted, PCR-amplifiable, human chromosome-specific painting probes, CYTOG C GEN, 84(3-4), 1999, pp. 233-240
Comparative genomic hybridization, loss of heterozygosity, and DNA sequence analysis of single cells
Authors: Klein, CA Schmidt-Kittler, O Schardt, JA Pantel, K Speicher, MR Riethmuller, G
Citation: Ca. Klein et al., Comparative genomic hybridization, loss of heterozygosity, and DNA sequence analysis of single cells, P NAS US, 96(8), 1999, pp. 4494-4499
Frequent chromosomal DNA unbalance in thyroid oncocytic (Hurthle cell) neoplasms detected by comparative genomic hybridization
Authors: Tallini, G Hsueh, A Liu, S Garcia-Rostan, G Speicher, MR Ward, DC
Citation: G. Tallini et al., Frequent chromosomal DNA unbalance in thyroid oncocytic (Hurthle cell) neoplasms detected by comparative genomic hybridization, LAB INV, 79(5), 1999, pp. 547-555
Risultati: 1-25 | 26-27