Works matching IS 03010171 AND DT 2000 AND VI 90 AND IP 1/2
Results: 30
Report of the third international workshop on human chromosome 10 mapping and sequencing 1999.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 1, doi. 10.1159/000015653
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Mini review: Form and function in the human interphase chromosome.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 13, doi. 10.1159/000015654
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Cloning of leptin cDNA and assignment to the long arm of chromosome 5 in the marsupial Sminthopsis crassicaudata.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 22, doi. 10.1159/000015655
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Characterization of three hairy cell leukemia- derived cell lines (ESKOL, JOK-1, and Hair-M) by multiplex-FISH, comparative genomic hybridization, FISH, PRINS, and dideoxyPRINS.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 30, doi. 10.1159/000015656
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Differential increase of steroid sulfatase activity in XX and XY trophoblast cells from human term placenta with syncytia formation in vitro.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 40, doi. 10.1159/000015657
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Human secretin (SCT): gene structure, chromosome location, and distribution of mRNA.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 47, doi. 10.1159/000015658
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Genetic and physical mapping of the porcine melatonin receptor 1B gene (MTNR1B) to chromosome 9.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 53, doi. 10.1159/000015659
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the Centromere Protein H (Cenph) gene to mouse chromosome band 13D1 by in situ hybridization and interspecific backcross analyses.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 56, doi. 10.1159/000015660
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Assignment<FOOTREF>[sup 1] </FOOTREF> of Karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 58, doi. 10.1159/000015661
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The human inward rectifier K[sup +] channel subunit Kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 60, doi. 10.1159/000015662
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the MDM2 binding protein gene (MTBP) to human chromosome band 8q24 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 64, doi. 10.1159/000015663
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the canine paired-box 3 (PAX3) gene to chromosome 37q16→q17 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 66, doi. 10.1159/000015664
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Assignment of transcription factor NFAT5 to human chromosome 16q22.1, murine chromosome 8D and porcine chromosome 6p1.4 and comparison of the polyglutamine domains.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 68, doi. 10.1159/000015665
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Expression and comparative chromosomal mapping of MKP-5 genes DUSP10/Dusp10.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 71, doi. 10.1159/000015666
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Molecular cloning, expression and chromosome location of the human pelota gene PELO.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 75, doi. 10.1159/000015667
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Spontaneous frequencies of aneuploid and diploid sperm in 10 normal Chinese men: assessed by multicolor fluorescence in situ hybridization.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 79, doi. 10.1159/000015668
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Assignment<FOOTREF>[sup 1] </FOOTREF> of BCAT1, the gene encoding cytosolic branched chain aminotransferase, to sheep chromosome band 3q33 and to cattle and goat chromosome bands 5q33 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 84, doi. 10.1159/000015669
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Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 86, doi. 10.1159/000015640
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DNA methylation and chromosome instability in lymphoblastoid cell lines.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 93, doi. 10.1159/000015641
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Thirteen type I loci from HSA4q, HSA6p, HSA7q and HSA12q were comparatively FISH-mapped in four river buffalo and sheep chromosomes.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 102, doi. 10.1159/000015642
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Isolation and characterization of a new FHL1 variant (FHL1C) from porcine skeletal muscle.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 106, doi. 10.1159/000015643
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Genomic structure and chromosome mapping of human and mouse RAMP genes.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 115, doi. 10.1159/000015644
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No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD).
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 119, doi. 10.1159/000015645
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Assignment<FOOTREF>[sup 1] </FOOTREF> of Microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 123, doi. 10.1159/000015646
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Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 126, doi. 10.1159/000015647
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Chromosome mapping of the genes for murine arylamine N -acetyltransferases (NATs), enzymes involved in the metabolism of carcinogens: identification of a novel upstream noncoding exon for murine Nat2.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 134, doi. 10.1159/000015648
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Organization of telomere sequences in birds: evidence for arrays of extreme length and for in vivo shortening.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 139, doi. 10.1159/000015649
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Cloning and chromosomal mapping of the mouse and human genes encoding the orphan glucocorticoid-induced receptor (GPR83).
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 146, doi. 10.1159/000015650
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Clustering of two fragile sites and seven homeobox genes in human chromosome region 2q31→q32.1.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 151, doi. 10.1159/000015651
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The 36th American Cytogenetics Conference.
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- Cytogenetics & Cell Genetics, 2000, v. 90, n. 1/2, p. 154, doi. 10.1159/000015652
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- Article