Published in Adv Hum Genet on January 01, 1982
Directional cloning of DNA fragments at a large distance from an initial probe: a circularization method. Proc Natl Acad Sci U S A (1984) 7.38
Human lymphotoxin and tumor necrosis factor genes: structure, homology and chromosomal localization. Nucleic Acids Res (1985) 5.22
Chromosomal location of the co-expressed human skeletal and cardiac actin genes. Proc Natl Acad Sci U S A (1984) 2.36
Human cardiac myosin heavy chain genes and their linkage in the genome. Nucleic Acids Res (1987) 2.22
Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain. Proc Natl Acad Sci U S A (1985) 2.03
Developmental Anomalies in Farm Animals: II. Defining Etiology. Can Vet J (1988) 1.92
A truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignment. J Cell Biol (1992) 1.84
Gene structure, chromosomal location, and basis for alternative mRNA splicing of the human VCAM1 gene. Proc Natl Acad Sci U S A (1991) 1.79
Cloning of the chromosome translocation breakpoint junction of the t(14;19) in chronic lymphocytic leukemia. Proc Natl Acad Sci U S A (1987) 1.75
Isolation of polymorphic DNA segments from human chromosome 21. Nucleic Acids Res (1985) 1.66
Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma. J Clin Invest (1989) 1.64
Human immune interferon gene is located on chromosome 12. J Exp Med (1983) 1.64
Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues. J Cell Biol (1994) 1.57
Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease. Proc Natl Acad Sci U S A (1988) 1.47
Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27. Am J Hum Genet (1987) 1.43
Localization of the human gene allowing infection by gibbon ape leukemia virus to human chromosome region 2q11-q14 and to the homologous region on mouse chromosome 2. J Virol (1991) 1.37
The human TTP protein: sequence, alignment with related proteins, and chromosomal localization of the mouse and human genes. Nucleic Acids Res (1991) 1.35
A group of type I keratin genes on human chromosome 17: characterization and expression. Mol Cell Biol (1988) 1.27
DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22. Proc Natl Acad Sci U S A (1984) 1.22
c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemia. J Exp Med (1983) 1.19
The core polypeptide of cystic fibrosis tracheal mucin contains a tandem repeat structure. Evidence for a common mucin in airway and gastrointestinal tissue. J Clin Invest (1990) 1.16
Human salivary proline-rich protein genes on chromosome 12. Am J Hum Genet (1985) 1.14
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe. J Med Genet (1983) 1.13
Identification of a single chromosome in the normal human genome essential for suppression of hamster cell transformation. Proc Natl Acad Sci U S A (1985) 1.12
Human gene map. Am J Hum Genet (1983) 1.11
Assignment of the human 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible cytochrome P1-450 gene to chromosome 15. Nucleic Acids Res (1985) 1.08
Two nonallelic tRNAiMet genes are located in the p23 leads to q12 region of human chromosome 6. Proc Natl Acad Sci U S A (1983) 1.07
Developmental anomalies in farm animals: I. Theoretical considerations. Can Vet J (1988) 1.06
Two human relaxin genes are on chromosome 9. EMBO J (1984) 0.91
A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs. Am J Hum Genet (1991) 0.90
Novel DNA sequences at chromosome 10q26 are amplified in human gastric carcinoma cell lines: molecular cloning by competitive DNA reassociation. Nucleic Acids Res (1991) 0.89
Human monocyte Arg-Serpin cDNA. Sequence, chromosomal assignment, and homology to plasminogen activator-inhibitor. J Exp Med (1987) 0.88
The gene for the alpha i1 subunit of human guanine nucleotide binding protein maps near the cystic fibrosis locus. Am J Hum Genet (1988) 0.86
The human salivary protein complex (SPC): a large block of related genes. Am J Hum Genet (1985) 0.84
Different forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16. Mol Cell Biol (1991) 0.84
Regional localization of two human cellular Kirsten ras genes on chromosomes 6 and 12. Mol Cell Biol (1984) 0.80
Construction and analysis of DNA sequence libraries from flow-sorted chromosomes: practical and theoretical considerations. Nucleic Acids Res (1984) 0.79
The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation. Am J Hum Genet (1990) 0.79
Characterization of a Chinese hamster-human hybrid cell line with increased system L amino acid transport activity. Mol Cell Biol (1984) 0.77
Pigment-cell-specific genes from fibroblasts are transactivated after chromosomal transfer into melanoma cells. Mol Cell Biol (1994) 0.77
The gene for the human mast cell high-affinity IgE receptor alpha chain: chromosomal localization to Iq21-q23 and RFLP analysis. Am J Hum Genet (1989) 0.75
Chromosomal trisomy in an anormalous bovine fetus. Can Vet J (1987) 0.75
Human biochemical genetics of enzyme proteins in the new age of molecular genetics. J Inherit Metab Dis (1986) 0.75
Initial sequencing and analysis of the human genome. Nature (2001) 212.86
A polymorphic DNA marker genetically linked to Huntington's disease. Nature (1984) 16.71
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science (2001) 7.34
Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein. Proc Natl Acad Sci U S A (1988) 7.26
A zinc finger-encoding gene coregulated with c-fos during growth and differentiation, and after cellular depolarization. Cell (1988) 6.62
Structure and variability of human chromosome ends. Mol Cell Biol (1990) 6.18
Molecular genetics of inherited variation in human color vision. Science (1986) 5.28
Human lymphotoxin and tumor necrosis factor genes: structure, homology and chromosomal localization. Nucleic Acids Res (1985) 5.22
cDNA sequence and chromosomal localization of human platelet-derived growth factor A-chain and its expression in tumour cell lines. Nature (1986) 4.81
A human amphotropic retrovirus receptor is a second member of the gibbon ape leukemia virus receptor family. Proc Natl Acad Sci U S A (1994) 3.42
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc Natl Acad Sci U S A (1999) 3.37
Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues. J Biol Chem (1988) 3.18
The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons. J Neurosci (1995) 2.94
Nonspecific integration of the HTLV provirus genome into adult T-cell leukaemia cells. Nature (1984) 2.78
Structural organization and chromosomal assignment of the gene encoding endothelin. J Biol Chem (1989) 2.77
Molecular cloning, sequencing, and mapping of EGR2, a human early growth response gene encoding a protein with "zinc-binding finger" structure. Proc Natl Acad Sci U S A (1988) 2.73
Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35. Diabetes (1987) 2.72
Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer. Nature (1987) 2.59
International system for human gene nomenclature (1979) ISGN (1979). Cytogenet Cell Genet (1979) 2.58
Human apolipoprotein B-100: cloning, analysis of liver mRNA, and assignment of the gene to chromosome 2. Proc Natl Acad Sci U S A (1985) 2.53
Identification of a new endothelial cell growth factor receptor tyrosine kinase. Oncogene (1991) 2.39
Structure of the human and murine R-ras genes, novel genes closely related to ras proto-oncogenes. Cell (1987) 2.36
Chromosome localization in normal human cells and neuroblastomas of a gene related to c-myc. Nature (1984) 2.32
The 1985 Catalog of Mapped Genes and report of the Nomenclature Committee. Cytogenet Cell Genet (1985) 2.24
Assignment of the beta-glucuronidase structural gene to the pter leads to q22 region of chromosome 7 in man. Cytogenet Cell Genet (1978) 2.22
Human cardiac myosin heavy chain genes and their linkage in the genome. Nucleic Acids Res (1987) 2.22
A single copy subclone, p1-101, from cosmid 3-3B, defines three RFLPs on 10pter-q23 [HGM9 no. D10S4]. Nucleic Acids Res (1987) 2.12
Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome. Proc Natl Acad Sci U S A (1990) 2.04
The insulin gene is located on chromosome 11 in humans. Nature (1980) 2.03
Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain. Proc Natl Acad Sci U S A (1985) 2.03
EGR3, a novel member of the Egr family of genes encoding immediate-early transcription factors. Oncogene (1991) 2.01
The insulin gene is located on the short arm of chromosome 11 in humans. Diabetes (1981) 2.00
Leukocyte and fibroblast interferon genes are located on human chromosome 9. Proc Natl Acad Sci U S A (1981) 1.98
Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells. Neuron (1993) 1.88
High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization. Proc Natl Acad Sci U S A (1983) 1.87
Human transferrin: cDNA characterization and chromosomal localization. Proc Natl Acad Sci U S A (1984) 1.85
Genes for growth hormone, chorionic somatommammotropin, and growth hormones-like gene on chromosome 17 in humans. Science (1980) 1.85
Complete amino acid sequence of human cartilage link protein (CRTL1) deduced from cDNA clones and chromosomal assignment of the gene. Genomics (1990) 1.85
The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. Nature (1986) 1.84
A truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignment. J Cell Biol (1992) 1.84
Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes. Adv Cancer Res (1997) 1.81
Cloning of the chromosome translocation breakpoint junction of the t(14;19) in chronic lymphocytic leukemia. Proc Natl Acad Sci U S A (1987) 1.75
Multigene family for sarcomeric myosin heavy chain in mouse and human DNA: localization on a single chromosome. Science (1983) 1.74
Human beta-D-N-acetylhexosaminidases A and B: expression and linkage relationships in somatic cell hybrids. Proc Natl Acad Sci U S A (1974) 1.71
Intrachromosomal genomic instability in human sporadic colorectal cancer measured by genome-wide allelotyping and inter-(simple sequence repeat) PCR. Cancer Res (2001) 1.69
Chromosomal localization of the human apoprotein CI gene and of a polymorphic apoprotein AII gene. Biochem Biophys Res Commun (1984) 1.69
Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc Natl Acad Sci U S A (1990) 1.68
Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7. Nature (1985) 1.66
Isolation of polymorphic DNA segments from human chromosome 21. Nucleic Acids Res (1985) 1.66
Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma. J Clin Invest (1989) 1.64
Human immune interferon gene is located on chromosome 12. J Exp Med (1983) 1.64
Localization of insulin-like growth factor genes to human chromosomes 11 and 12. Nature (1984) 1.58
PCR primers for human chromosomes: reagents for the rapid analysis of somatic cell hybrids. Genomics (1991) 1.58
Molecular cloning of cDNAs encoding the human bombesin-like peptide neuromedin B. Chromosomal localization and comparison to cDNAs encoding its amphibian homolog ranatensin. J Biol Chem (1988) 1.58
Positional cloning of a gene involved in hereditary multiple exostoses. Hum Mol Genet (1996) 1.58
Assignment of the pepsinogen gene complex (PGA) to human chromosome region 11q13 by in situ hybridization. Cytogenet Cell Genet (1986) 1.57
Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues. J Cell Biol (1994) 1.57
DNA sequence and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11. DNA (1987) 1.56
Enhanced levels of insulin-like growth factor messenger RNA in human colon carcinomas and liposarcomas. Cancer Res (1986) 1.55
Linkage-disequilibrium mapping without genotyping. Nat Genet (1998) 1.52
Deletion in chromosome 11p associated with a hepatitis B integration site in hepatocellular carcinoma. Science (1985) 1.51
Hepatitis B virus integration site in hepatocellular carcinoma at chromosome 17;18 translocation. Proc Natl Acad Sci U S A (1986) 1.48
Molecular genetics of Alport syndrome. Kidney Int (1993) 1.48
Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease. Proc Natl Acad Sci U S A (1988) 1.47
Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain. Genomics (1998) 1.45
Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors. Oncogene (1991) 1.44
Human X-Linked genes regionally mapped utilizing X-autosome translocations and somatic cell hybrids. Proc Natl Acad Sci U S A (1975) 1.44
Human group-specific component (Gc) is a member of the albumin family. Proc Natl Acad Sci U S A (1985) 1.44
Tissue factor gene localized to human chromosome 1 (1pter----1p21). Science (1985) 1.43
Supercoil sequencing using unpurified templates produced by rapid boiling. Biotechniques (1988) 1.43
NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia. Cancer Res (1998) 1.42
Mapping of genes for the human C5a receptor (C5AR), human FMLP receptor (FPR), and two FMLP receptor homologue orphan receptors (FPRH1, FPRH2) to chromosome 19. Genomics (1992) 1.42
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis. Am J Hum Genet (1976) 1.41
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). Cytogenet Cell Genet (1987) 1.40
Human alpha 2-macroglobulin gene is located on chromosome 12. Somat Cell Mol Genet (1985) 1.40
Cloning of a novel tumor necrosis factor-alpha-inducible primary response gene that is differentially expressed in development and capillary tube-like formation in vitro. J Immunol (1992) 1.40
Characterization of the human and rat myoadenylate deaminase genes. J Biol Chem (1990) 1.40
Somatic cell genetic evidence for X-chromosome linkage of three enzymes in the mouse. Nature (1976) 1.39
Genetics of human-mouse somatic cell hybrids: linkage of human genes for lactate dehydrogenase-A and esterase-A 4 . Proc Natl Acad Sci U S A (1972) 1.38
Loss of heterozygosity in breast cancer: cause or effect? J Natl Cancer Inst (1989) 1.38
Localization of the human gene allowing infection by gibbon ape leukemia virus to human chromosome region 2q11-q14 and to the homologous region on mouse chromosome 2. J Virol (1991) 1.37
A model system to study genomic imprinting of human genes. Proc Natl Acad Sci U S A (1998) 1.35
The human TTP protein: sequence, alignment with related proteins, and chromosomal localization of the mouse and human genes. Nucleic Acids Res (1991) 1.35
Phospholipase C-148: chromosomal location and deletion mapping of functional domains. Cold Spring Harb Symp Quant Biol (1988) 1.33
Mitochondrial malate dehydrogenase and malic enzyme: Mendelian inherited electrophoretic variants in the mouse. Biochem Genet (1970) 1.33
Localization of the human prealbumin gene to chromosome 18. Biochem Biophys Res Commun (1985) 1.32
Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22----q24.1, 11p15, and 4q25----q27, respectively. Cytogenet Cell Genet (1986) 1.32