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Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genomic aberrations and survival in chronic lymphocytic leukemia. N Engl J Med 2000 16.30
2 Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer 1997 8.27
3 Role of chromosome territories in the functional compartmentalization of the cell nucleus. Cold Spring Harb Symp Quant Biol 1993 3.38
4 Expression of an ASCL2 related stem cell signature and IGF2 in colorectal cancer liver metastases with 11p15.5 gain. Gut 2010 3.24
5 Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet 1993 2.64
6 Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum Genet 1988 2.52
7 Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. Cancer Res 1998 2.41
8 Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation breakpoints with a yeast artificial chromosome. Proc Natl Acad Sci U S A 1990 2.29
9 Active and inactive genes localize preferentially in the periphery of chromosome territories. J Cell Biol 1996 2.25
10 Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30+ Hodgkin cells. Cancer Res 2000 2.09
11 Molecular characterization of a slowly gating human hyperpolarization-activated channel predominantly expressed in thalamus, heart, and testis. Proc Natl Acad Sci U S A 1999 2.07
12 Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and amplification of the REL gene. Blood 1996 1.85
13 DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation. Neurology 2007 1.81
14 Expressed sequences as candidates for a novel tumor suppressor gene at band 13q14 in B-cell chronic lymphocytic leukemia and mantle cell lymphoma. Oncogene 1998 1.81
15 Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics. Hum Genet 1990 1.81
16 Analysis of genomic alterations in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression. Proc Natl Acad Sci U S A 1997 1.76
17 Mutation of the PTEN (MMAC1) tumor suppressor gene in a subset of glioblastomas but not in meningiomas with loss of chromosome arm 10q. Cancer Res 1998 1.75
18 Quantitative analysis of comparative genomic hybridization. Cytometry 1995 1.72
19 Evidence for a nuclear compartment of transcription and splicing located at chromosome domain boundaries. Chromosome Res 1993 1.72
20 B-cell neoplasia associated gene with multiple splicing (BCMS): the candidate B-CLL gene on 13q14 comprises more than 560 kb covering all critical regions. Hum Mol Genet 2001 1.70
21 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis. Blood 1997 1.69
22 The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product. Genomics 1990 1.67
23 Mapping of chromosomal imbalances in pancreatic carcinoma by comparative genomic hybridization. Cancer Res 1996 1.63
24 Somatic ATM mutations indicate a pathogenic role of ATM in B-cell chronic lymphocytic leukemia. Blood 1999 1.55
25 Gain of chromosome arm 9p is characteristic of primary mediastinal B-cell lymphoma (MBL): comprehensive molecular cytogenetic analysis and presentation of a novel MBL cell line. Genes Chromosomes Cancer 2001 1.49
26 Amplification and expression of cyclin D genes (CCND1, CCND2 and CCND3) in human malignant gliomas. Brain Pathol 1999 1.48
27 De-repression of CTGF via the miR-17-92 cluster upon differentiation of human glioblastoma spheroid cultures. Oncogene 2010 1.47
28 Mantle cell lymphoma is characterized by inactivation of the ATM gene. Proc Natl Acad Sci U S A 2000 1.46
29 Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components. J Pathol 2006 1.45
30 Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development. Development 1996 1.44
31 Minimal sizes of deletions detected by comparative genomic hybridization. Genes Chromosomes Cancer 1998 1.42
32 Genomic imbalances are rare in hairy cell leukemia. Genes Chromosomes Cancer 1999 1.39
33 Three human elastase-like genes coordinately expressed in the myelomonocyte lineage are organized as a single genetic locus on 19pter. Proc Natl Acad Sci U S A 1992 1.38
34 Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders. Blood 1998 1.36
35 Nuclear envelope and chromatin compositional differences comparing undifferentiated and retinoic acid- and phorbol ester-treated HL-60 cells. Exp Cell Res 2001 1.35
36 Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization. Am J Pathol 1995 1.34
37 Genetics of chronic lymphocytic leukemia: genomic aberrations and V(H) gene mutation status in pathogenesis and clinical course. Leukemia 2002 1.33
38 Chromosomal localization of the four genes (NFIA, B, C, and X) for the human transcription factor nuclear factor I by FISH. Genomics 1995 1.27
39 Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas. Am J Pathol 2001 1.27
40 Partial characterization of the human beta-myosin heavy-chain gene which is expressed in heart and skeletal muscle. Eur J Biochem 1986 1.24
41 Mapping of chromosomal imbalances in gastric adenocarcinoma revealed amplified protooncogenes MYCN, MET, WNT2, and ERBB2. Genes Chromosomes Cancer 1998 1.23
42 Adrenocortical carcinoma is characterized by a high frequency of chromosomal gains and high-level amplifications. Genes Chromosomes Cancer 2000 1.23
43 CDNA microarray gene expression analysis of B-cell chronic lymphocytic leukemia proposes potential new prognostic markers involved in lymphocyte trafficking. Int J Cancer 2001 1.23
44 Retinoic acid differentiation of HL-60 cells promotes cytoskeletal polarization. Exp Cell Res 2000 1.23
45 Recurrent chromosomal imbalances detected in biopsy material from oral premalignant and malignant lesions by combined tissue microdissection, universal DNA amplification, and comparative genomic hybridization. Am J Pathol 1998 1.22
46 Chromosome aberrations in B-cell chronic lymphocytic leukemia: reassessment based on molecular cytogenetic analysis. J Mol Med (Berl) 1999 1.21
47 RNAi screening in glioma stem-like cells identifies PFKFB4 as a key molecule important for cancer cell survival. Oncogene 2011 1.20
48 Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias. Blood 1997 1.19
49 Identification of novel tumour-associated genes differentially expressed in the process of squamous cell cancer development. Oncogene 2006 1.19
50 Specific chromosomal imbalances in human papillomavirus-transfected cells during progression toward immortality. Proc Natl Acad Sci U S A 1997 1.17
51 Characterization of a high copy number amplification at 6q24 in pancreatic cancer identifies c-myb as a candidate oncogene. Cancer Res 1997 1.17
52 Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe. Hum Genet 1993 1.16
53 Association of pKi-67 with satellite DNA of the human genome in early G1 cells. Chromosome Res 1998 1.16
54 Biallelic mutations in the ATM gene in T-prolymphocytic leukemia. Nat Med 1997 1.13
55 H-1 parvovirus-associated replication bodies: a distinct virus-induced nuclear structure. J Virol 2000 1.12
56 Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses. Blood 1995 1.12
57 Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas. Oncogene 2006 1.12
58 Identification of an interchromosomal compartment by polymerization of nuclear-targeted vimentin. J Cell Sci 1998 1.11
59 Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis. J Pediatr 2000 1.11
60 Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization. Genes Chromosomes Cancer 1995 1.11
61 Transcriptional and translational downregulation of H-REV107, a class II tumour suppressor gene located on human chromosome 11q11-12. Oncogene 1998 1.10
62 Pbx4, a new Pbx family member on mouse chromosome 8, is expressed during spermatogenesis. Mech Dev 2001 1.09
63 The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcripts. J Biol Chem 1998 1.09
64 Image analysis in comparative genomic hybridization. Cytometry 1995 1.05
65 Cloning, expression, and chromosomal localization of the 140-kilodalton subunit of replication factor C from mice and humans. Mol Cell Biol 1994 1.05
66 Variable breakpoints in Burkitt lymphoma cells with chromosomal t(8;14) translocation separate c-myc and the IgH locus up to several hundred kb. Hum Mol Genet 1992 1.05
67 Expression analysis of imbalanced genes in prostate carcinoma using tissue microarrays. Br J Cancer 2006 1.03
68 Retinoic acid induction of nuclear envelope-limited chromatin sheets in HL-60. Exp Cell Res 1998 1.02
69 APM-1, a novel human gene, identified by aberrant co-transcription with papillomavirus oncogenes in a cervical carcinoma cell line, encodes a BTB/POZ-zinc finger protein with growth inhibitory activity. EMBO J 1998 1.02
70 Efficient nucleofection of primary human B cells and B-CLL cells induces apoptosis, which depends on the microenvironment and on the structure of transfected nucleic acids. Leukemia 2007 1.02
71 Centrosome amplification as a possible mechanism for numerical chromosome aberrations in cerebral primitive neuroectodermal tumors with TP53 mutations. Cytogenet Cell Genet 1998 1.01
72 High incidence of chromosomal imbalances and gene amplifications in the classical follicular variant of follicle center lymphoma. Blood 1996 1.01
73 Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-923.1 in lymphoproliferative disorders. Proc Natl Acad Sci U S A 1996 1.00
74 Molecular characterization of 11q deletions points to a pathogenic role of the ATM gene in mantle cell lymphoma. Blood 1999 1.00
75 Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes. Hum Genet 1992 1.00
76 Acromegaly caused by secretion of growth hormone by a non-Hodgkin's lymphoma. N Engl J Med 2000 1.00
77 Analysis of chromosomal imbalances in sporadic and NF1-associated peripheral nerve sheath tumors by comparative genomic hybridization. Genes Chromosomes Cancer 1999 0.99
78 Spatial distribution of GC- and AT-rich DNA sequences within human chromosome territories. Exp Cell Res 2000 0.98
79 Characterization and mapping of human genes encoding zinc finger proteins. Proc Natl Acad Sci U S A 1991 0.98
80 Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1. Hum Mol Genet 1995 0.98
81 Downregulation of PRDX1 by promoter hypermethylation is frequent in 1p/19q-deleted oligodendroglial tumours and increases radio- and chemosensitivity of Hs683 glioma cells in vitro. Oncogene 2011 0.97
82 Spleen-specific expression of the malaria-inducible intronless mouse gene imap38. J Biol Chem 1999 0.97
83 Characteristic pattern of chromosomal gains and losses in primary large B-cell lymphomas of the gastrointestinal tract. Blood 1998 0.96
84 Altered miRNA and gene expression in acute myeloid leukemia with complex karyotype identify networks of prognostic relevance. Leukemia 2012 0.96
85 High-level DNA amplifications are common genetic aberrations in B-cell neoplasms. Am J Pathol 1997 0.96
86 Human eukaryotic initiation factor EIF2C1 gene: cDNA sequence, genomic organization, localization to chromosomal bands 1p34-p35, and expression. Genomics 1999 0.96
87 Hypermethylation and transcriptional downregulation of the CITED4 gene at 1p34.2 in oligodendroglial tumours with allelic losses on 1p and 19q. Oncogene 2007 0.95
88 Human mitochondrial 3,2-trans-enoyl-CoA isomerase (DCI): gene structure and localization to chromosome 16p13.3. Genomics 1994 0.95
89 Cytogenetic and molecular cytogenetic analysis of B cell chronic lymphocytic leukemia: specific chromosome aberrations identify prognostic subgroups of patients and point to loci of candidate genes. Leukemia 1997 0.95
90 Gene structure and chromosomal localization of the murine lamin B2 gene. Eur J Cell Biol 1991 0.94
91 t(11;14)-positive mantle cell lymphomas exhibit complex karyotypes and share similarities with B-cell chronic lymphocytic leukemia. Genes Chromosomes Cancer 2000 0.94
92 Functional characterization of the gene encoding RLIM, the corepressor of LIM homeodomain factors. Genomics 2000 0.94
93 Human homeodomain-interacting protein kinase-2 (HIPK2) is a member of the DYRK family of protein kinases and maps to chromosome 7q32-q34. Biochimie 2000 0.94
94 Repetin (Rptn), a new member of the "fused gene" subgroup within the S100 gene family encoding a murine epidermal differentiation protein. Genomics 1997 0.94
95 High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2. Genes Chromosomes Cancer 1997 0.93
96 Genetic features of B-cell chronic lymphocytic leukemia. Rev Clin Exp Hematol 2000 0.93
97 In vivo observation of a nuclear channel-like system: evidence for a distinct interchromosomal domain compartment in interphase cells. J Struct Biol 2000 0.93
98 Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis? Ann Hematol 2007 0.92
99 A novel orphan G protein-coupled receptor primarily expressed in the brain is localized on human chromosomal band 2q21. J Neurochem 1998 0.92
100 Further delineation of chromosomal consensus regions in primary mediastinal B-cell lymphomas: an analysis of 37 tumor samples using high-resolution genomic profiling (array-CGH). Leukemia 2007 0.92
101 Amplification of Cyclin L1 is associated with lymph node metastases in head and neck squamous cell carcinoma (HNSCC). Br J Cancer 2005 0.92
102 Incidence and clinical significance of 6q deletions in B cell chronic lymphocytic leukemia. Leukemia 1999 0.91
103 Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization. Oncogene 1994 0.91
104 Detection of chimeric BCR-ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization. Blood 1994 0.91
105 Primary structure, chromosomal mapping, expression and transcriptional activity of murine hepatocyte nuclear factor 4gamma. Biochim Biophys Acta 2000 0.90
106 The human homolog of the glomerulosclerosis gene Mpv17: structure and genomic organization. Hum Mol Genet 1993 0.90
107 Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics. Cytogenet Cell Genet 2000 0.90
108 Generation of transgenic mice with yeast artificial chromosomes. Cold Spring Harb Symp Quant Biol 1993 0.89
109 Chordoid glioma of the third ventricle: immunohistochemical and molecular genetic characterization of a novel tumor entity. Brain Pathol 1999 0.89
110 Genomic organization of mouse gene zfp162. DNA Cell Biol 1999 0.89
111 Molecular cytogenetic analysis of B-cell chronic lymphocytic leukemia. Ann Hematol 1998 0.88
112 Chromosome imbalances in papillary renal cell carcinoma and first cytogenetic data of familial cases analyzed by comparative genomic hybridization. Cytogenet Cell Genet 1996 0.88
113 Design and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia. Blood 1996 0.88
114 Cloning and structure of the gene encoding the human N-methyl-D-aspartate receptor (NMDAR1). Gene 1995 0.87
115 Cloning of the VASP (vasodilator-stimulated phosphoprotein) genes in human and mouse: structure, sequence, and chromosomal localization. Genomics 1996 0.87
116 Human casein kinase II subunit alpha: sequence of a processed (pseudo)gene and its localization on chromosome 11. Biochim Biophys Acta 1992 0.87
117 Human clusterin (CLI) maps to 8p21 in proximity to the lipoprotein lipase (LPL) gene. Genomics 1993 0.87
118 Regional localisation of the Friedreich ataxia locus to human chromosome 9q13----q21.1. Cytogenet Cell Genet 1990 0.87
119 The human Met-ase gene (GZMM): structure, sequence, and close physical linkage to the serine protease gene cluster on 19p13.3. Genomics 1994 0.87
120 Loss of the Y chromosome is a frequent chromosomal imbalance in pancreatic cancer and allows differentiation to chronic pancreatitis. Int J Cancer 2001 0.87
121 Comparative genomic hybridization in the investigation of myeloid leukemias. Genes Chromosomes Cancer 1995 0.86
122 Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization. Genes Chromosomes Cancer 1996 0.86
123 Rapid analysis of mouse-hamster hybrid cell lines by in situ hybridization. Genomics 1990 0.86
124 Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization. Cytometry 1990 0.86
125 Characteristic chromosomal imbalances in primary central nervous system lymphomas of the diffuse large B-cell type. Brain Pathol 2000 0.86
126 Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs. Genomics 1997 0.85
127 DNA microarray analysis in malignant lymphomas. Ann Hematol 2003 0.85
128 Heterogeneity of the API2-MALT1 gene rearrangement in MALT-type lymphoma. Leukemia 2000 0.85
129 Construction of a gene map of the nephronophthisis type 1 (NPHP1) region on human chromosome 2q12-q13. Genomics 1998 0.85
130 Murine epidermal lipoxygenase (Aloxe) encodes a 12-lipoxygenase isoform. FEBS Lett 1997 0.85
131 The extended packaging sequence of MoMLV contains a constitutive mRNA nuclear export function. FEBS Lett 1998 0.85
132 MDM2 gene amplification and lack of p53 point mutations in Hodgkin and Reed-Sternberg cells: results from single-cell polymerase chain reaction and molecular cytogenetic studies. Br J Haematol 2001 0.85
133 Nucleocytoplasmic transport of HTLV-1 RNA is regulated by two independent LTR encoded nuclear retention elements. Oncogene 1998 0.84
134 Integration of human papillomavirus type 6a DNA in a tonsillar carcinoma: chromosomal localization and nucleotide sequence of the genomic target region. Cancer Res 1994 0.84
135 Topological organization of the MYC/IGK locus in Burkitt's lymphoma cells assessed by nuclear halo preparations. Exp Cell Res 2002 0.84
136 The ATM gene in the pathogenesis of mantle-cell lymphoma. Ann Oncol 2000 0.83
137 Trisomy 12 in chronic lymphoid leukemias--a metaphase and interphase cytogenetic analysis. Leukemia 1993 0.83
138 Complete sequence, genomic organization, and chromosomal localization of the human gene encoding the SHP2-interacting transmembrane adaptor protein (SIT). Immunogenetics 2001 0.83
139 Nuclear RNA accumulations contain released transcripts and exhibit specific distributions with respect to Sm antigen foci. DNA Cell Biol 1997 0.83
140 FGFR4 Arg388 genotype is associated with pathological complete response to neoadjuvant chemotherapy for primary breast cancer. Ann Oncol 2010 0.82
141 The mouse fkh-2 gene. Implications for notochord, foregut, and midbrain regionalization. J Biol Chem 1995 0.82
142 Novel technology for detection of genomic and transcriptional alterations in pancreatic cancer. Ann Oncol 1999 0.82
143 Analysis of human meningiomas for aberrations of the MADH2, MADH4, APM-1 and DCC tumor suppressor genes on the long arm of chromosome 18. Int J Cancer 2001 0.82
144 Effects of mycophenolic acid on human fibroblast proliferation, migration and adhesion in vitro and in vivo. Am J Transplant 2008 0.82
145 Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome. Am J Pathol 2000 0.82
146 Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes. Cytogenet Cell Genet 1991 0.81
147 Low grade fibromyxoid sarcoma. a further low-grade soft tissue malignancy characterized by a ring chromosome. Cancer Genet Cytogenet 2000 0.81
148 Gene knockdown studies revealed CCDC50 as a candidate gene in mantle cell lymphoma and chronic lymphocytic leukemia. Leukemia 2009 0.81
149 The human gene (CSNK2A1) coding for the casein kinase II subunit alpha is located on chromosome 20 and contains tandemly arranged Alu repeats. Genomics 1994 0.81
150 Mapping and chromosome analysis: the potential of fluorescence in situ hybridization. J Biotechnol 1994 0.81
151 Fliih, the murine homologue of the Drosophila melanogaster flightless I gene: nucleotide sequence, chromosomal mapping and overlap with Llglh. DNA Seq 2000 0.81
152 Direct visual resolution of gene copy number in the human photopigment gene array. Invest Ophthalmol Vis Sci 1999 0.81
153 High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood 1993 0.81
154 Sequence data and chromosomal localization of human type I and type II hair keratin genes. Exp Cell Res 1995 0.81
155 DNA chip technology ante portas. J Mol Med (Berl) 1999 0.81
156 Risk of false positive results in comparative genomic hybridization. Genes Chromosomes Cancer 2000 0.81
157 Predetermined chromosomal deletion encompassing the Nf-1 gene. Oncogene 1999 0.80
158 High-resolution comparative hybridization to combed DNA fibers. Hum Genet 1997 0.80
159 Detection of trisomy 8 on blood smears using fluorescence in situ hybridization. Leukemia 1993 0.80
160 Retention of polysomy at 9p23-24 during karyotypic evolution in human breast cancer cell line COLO 824. Genes Chromosomes Cancer 1999 0.80
161 A transcribed human sequence related to the mouse HC1 and the human papillomavirus type 18 E5 genes is located at chromosome 7p13-14. Hum Mol Genet 1995 0.80
162 Hardware and software requirements for quantitative analysis of comparative genomic hybridization. Cytometry 1995 0.80
163 Mapping the beta NGF gene in situ to a microchromosome in chicken. Genomics 1992 0.80
164 Localization of the gene encoding the putative human HLA class II associated protein (PHAPI) to chromosome 15q22.3-q23 by fluorescence in situ hybridization. Genomics 1995 0.80
165 Human perforin (PRF1) maps to 10q22, a region that is syntenic with mouse chromosome 10. Genomics 1992 0.80
166 Isolation and characterization of the complete human beta-myosin heavy chain gene. Hum Genet 1989 0.79
167 [Analysis of chromosome copy number changes in leiomyosarcoma through molecular cytogenetic methods]. Verh Dtsch Ges Pathol 1998 0.79
168 Association of genomic imbalances with resistance to therapeutic drugs in human melanoma cell lines. Cytogenet Cell Genet 1999 0.79
169 Human neutral amino acid transporter ASCT1: structure of the gene (SLC1A4) and localization to chromosome 2p13-p15. Genomics 1994 0.79
170 A database system for comparative genomic hybridization analysis. IEEE Eng Med Biol Mag 2001 0.79
171 Overexpression of human poly(ADP-ribose) polymerase in transfected hamster cells leads to increased poly(ADP-ribosyl)ation and cellular sensitization to gamma irradiation. Eur J Biochem 1997 0.79
172 Protein expression analysis of chromosome 12 candidate genes in chronic lymphocytic leukemia (CLL). Leukemia 2005 0.79
173 Genomic organization and chromosomal localization of the human gene encoding the T-cell receptor-interacting molecule (TRIM). Immunogenetics 2000 0.79
174 Delineation of genomic regions in chromosome band 7q22 commonly deleted in myeloid leukemias. Recent Results Cancer Res 1998 0.78
175 The mouse filensin gene: structure and evolutionary relation to other intermediate filament genes. FEBS Lett 1997 0.78
176 Assignment of TRADD to human chromosome band 16q22 by in situ hybridization. Cytogenet Cell Genet 2001 0.78
177 Chromosomal imbalances associated with response to chemotherapy and cytotoxic cytokines in human malignant glioma cell lines. Int J Cancer 2001 0.78
178 Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization. Cancer Res 1995 0.78
179 Genetic and physical mapping and population studies of a fibronectin receptor beta-subunit-like sequence on human chromosome 19. Genomics 1990 0.78
180 Assignment of CASP8 to human chromosome band 2q33-->q34 and Casp8 to the murine syntenic region on chromosome 1B-proximal C by in situ hybridization. Cytogenet Cell Genet 1998 0.78
181 Human protein kinase CK2 genes. Cell Mol Biol Res 1994 0.78
182 Assignment of the human genes for hepatocyte nuclear factor 3-alpha, -beta, and -gamma (HNF3A, HNF3B, HNF3G) to 14q12-q13, 20p11, and 19q13.2-q13.4. Genomics 1997 0.78
183 Molecular cytogenetic analysis of RB-1 deletions in chronic B-cell leukemias. Leuk Lymphoma 1994 0.77
184 Genomic organization and subchromosomal in situ localization of the murine granzyme F, a serine protease expressed in CD8+ T cells. J Immunol 1991 0.77
185 Diagnosis and monitoring of chromosome aberrations in hematological malignancies by fluorescence in situ hybridization. Stem Cells 1995 0.77
186 Germ line transmission of yeast artificial chromosomes in transgenic mice. Reprod Fertil Dev 1994 0.77
187 Human high affinity, Na(+)-dependent L-glutamate/L-aspartate transporter GLAST-1 (EAAT-1): gene structure and localization to chromosome 5p11-p12. FEBS Lett 1996 0.77
188 The human glycine receptor beta subunit gene (GLRB): structure, refined chromosomal localization, and population polymorphism. Genomics 1998 0.77
189 BCMSUN, a candidate gene for B-cell chronic lymphocytic leukemia and mantle-cell lymphoma, has an independently expressed homolog on 1p22-p31, BCMSUN-like. Int J Cancer 2000 0.77
190 Assignment of the human homologue of the mouse t-complex gene TCTE3 to human chromosome 6q27. Genomics 1992 0.76
191 The human vitronectin (complement S-protein) gene maps to the centromeric region of 17q. Hum Genet 1992 0.76
192 BCL10 is not the gene inactivated by mutation in the 1p22 deletion region in mantle cell lymphoma. Leukemia 2000 0.76
193 Localization of the gene encoding the Ran-binding protein RanBP2 to human chromosome 2q11-q13 by fluorescence in situ hybridization. Genomics 1997 0.76
194 Interphase FISH in chronic lymphoproliferative disorders and comparative genomic hybridisation in the study of lymphomas. Haematologica 1999 0.76
195 Genomic organization, chromosomal localization and promoter function of the human zinc-finger gene pAT133. Hum Mol Genet 1993 0.76
196 The human granzyme A (HFSP, CTLA3) gene maps to 5q11-q12 and defines a new locus of the serine protease superfamily. Genomics 1993 0.76
197 [Opportunities and chances for tissue chip microarrays in head and neck surgery. A novel technique for the rapid evaluation of potentially novel biomarkers]. Mund Kiefer Gesichtschir 2002 0.75
198 Assignment of the gene encoding centrosome-associated protein CCD41 to mouse chromosome 2H. Mamm Genome 1995 0.75
199 [A new dimension of DNA analysis: genomic profiling by matrix CGH]. Verh Dtsch Ges Pathol 2003 0.75
200 Sequence, genomic organization, and chromosomal localization of the human LPAP (PTPRCAP) and mouse CD45-AP/LSM-1 genes. Genomics 1996 0.75
201 An indoor navigation system to support the visually impaired. Conf Proc IEEE Eng Med Biol Soc 2008 0.75
202 [Molecular pathology of sarcomas. Update on the research group "Molecular Diagnosis of Sarcomas"]. Pathologe 2010 0.75
203 The centrosomal protein centrosomin A and the nuclear protein centrosomin B derive from one gene by post-transcriptional processes involving RNA editing. J Cell Sci 1997 0.75
204 High incidence of a second BCR-ABL fusion in chronic myeloid leukemia revealed by interphase cytogenetic analysis on blood and bone marrow smears. Cancer Genet Cytogenet 1996 0.75
205 Fluorescence in situ hybridization in leukemias: 'the FISH are spawning!'. Leukemia 1994 0.75
206 Strategies for the detection of disease genes in pancreatic cancer. Ann N Y Acad Sci 1999 0.75
207 Molecular cytogenetic analysis of low-grade B-cell neoplasias: a comparative genomic hybridization study. Recent Results Cancer Res 1998 0.75
208 Cosmid linking clones localized to the long arm of human chromosome 11. Genomics 1992 0.75
209 Potential of chromosomal and matrix-based comparative genomic hybridization for molecular diagnostics in lymphomas. Ann Hematol 2001 0.75
210 Assignment of the human serine/threonine protein phosphatase 4 gene (PPP4C) to chromosome 16p11-p12 by fluorescence in situ hybridization. Genomics 1997 0.75
211 Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1. Cytogenet Cell Genet 1996 0.75
212 Bovine desmocollin genes (DSC1, DSC2, DSC3) cluster on chromosome 24q21/q22. Mamm Genome 1995 0.75
213 Localization of the novel serine/threonine protein phosphatase 6 gene (PPP6C) to human chromosome Xq22.3. Genomics 1997 0.75
214 The human gene for nuclear protein BM28 (CDCL1), a new member of the early S-phase family of proteins, maps to chromosome band 3q21. Cytogenet Cell Genet 1994 0.75
215 The human rab GDI beta gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13. Mamm Genome 1998 0.75
216 Primitive neuroectodermal tumors of the cerebral hemispheres in two siblings with TP53 germline mutation. J Neuropathol Exp Neurol 1998 0.75
217 Reciprocal translocation t(12;13)(p13;q14) in acute nonlymphoblastic leukemia: report and cytogenetic analysis of two cases. Cancer Genet Cytogenet 1994 0.75