Published in Genomics on October 01, 1994
The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4. Genome Res (1997) 1.50
Aurora kinase B modulates chromosome alignment in mouse oocytes. Mol Reprod Dev (2009) 1.12
Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints. Genome Res (2000) 1.10
Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1. Am J Hum Genet (1995) 1.01
Identification and characterization of the human homologue of the short PDE4A cAMP-specific phosphodiesterase RD1 (PDE4A1) by analysis of the human HSPDE4A gene locus located at chromosome 19p13.2. Biochem J (1998) 0.94
Location of mouse and human genes corresponding to conserved canine olfactory receptor gene subfamilies. Mamm Genome (1998) 0.77
In situ hybridization for the detection of rust fungi in paraffin embedded plant tissue sections. Plant Methods (2016) 0.75
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature (1998) 10.35
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell (1996) 5.99
Complications of diagnostic and therapeutic ERCP: a prospective multicenter study. Am J Gastroenterol (2001) 4.14
Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange. Mol Cell Biol (1990) 3.80
Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution. Science (2001) 3.39
A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange. Mutat Res (1982) 2.92
Sequence-specific identification of 18 pathogenic microorganisms using microarray technology. Mol Cell Probes (2002) 2.70
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nat Genet (1995) 2.55
Chromosome measurement and sorting by flow systems. Proc Natl Acad Sci U S A (1975) 2.37
Sequences required for coordinate induction of adeno-associated virus p19 and p40 promoters by Rep protein. J Virol (1991) 2.31
Genetic characterization of Gainj- and Kalam-speaking peoples of Papua New Guinea. Am J Phys Anthropol (1986) 2.28
Human ret proto-oncogene mapped to chromosome 10q11.2. Oncogene (1989) 2.17
Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells. Somat Cell Mol Genet (1985) 1.91
Microevolution in lower Central America: genetic characterization of the Chibcha-speaking groups of Costa Rica and Panama, and a consensus taxonomy based on genetic and linguistic affinity. Am J Hum Genet (1990) 1.86
A high-resolution, fluorescence-based, semiautomated method for DNA fingerprinting. Genomics (1989) 1.75
Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Hum Mol Genet (1997) 1.70
HIV-1 induces cytotoxic T lymphocytes in the cervix of infected women. J Exp Med (1997) 1.69
Sister chromatid exchange as an indicator of mutagenesis. Nature (1978) 1.68
Assignment of human beta-, gamma-, and delta-globin genes to the short arm of chromosome 11 by chromosome sorting and DNA restriction enzyme analysis. Proc Natl Acad Sci U S A (1979) 1.67
Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions. Genomics (1995) 1.67
Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity. Carcinogenesis (2001) 1.63
Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes. Cold Spring Harb Symp Quant Biol (1986) 1.62
Quantitative karyotyping of human chromosomes by dual beam flow cytometry. Proc Natl Acad Sci U S A (1982) 1.62
Measurement and purification of human chromosomes by flow cytometry and sorting. Proc Natl Acad Sci U S A (1979) 1.58
An integrated metric physical map of human chromosome 19. Nat Genet (1995) 1.54
Gene expression changes in mouse brain after exposure to low-dose ionizing radiation. Int J Radiat Biol (2003) 1.54
Cloning and characterization of HARP/SMARCAL1: a prokaryotic HepA-related SNF2 helicase protein from human and mouse. Genomics (2000) 1.52
Functional characterization of Ape1 variants identified in the human population. Nucleic Acids Res (2000) 1.50
Genetic studies on the Ticuna, an enigmatic tribe of Central Amazonas. Ann Hum Genet (1980) 1.49
Rate of spontaneous mutation at human loci encoding protein structure. Proc Natl Acad Sci U S A (1980) 1.49
Identification of a novel human RAD51 homolog, RAD51B. Genomics (1997) 1.49
An evaluation of the mouse sperm morphology test and other sperm tests in nonhuman mammals. A report of the U.S. Environmental Protection Agency Gene-Tox Program. Mutat Res (1983) 1.49
Cognitive impact of genetic variation of the serotonin transporter in primates is associated with differences in brain morphology rather than serotonin neurotransmission. Mol Psychiatry (2009) 1.42
Evolution of the mammalian G protein alpha subunit multigene family. Nat Genet (1992) 1.41
Chromosomes of human sperm: variability among normal individuals. Hum Genet (1985) 1.40
A transcript map of the chromosome 19q-arm glioma tumor suppressor region. Genomics (2000) 1.39
[Influenza vaccination of citizens of Copenhagen aged 70 years and more]. Ugeskr Laeger (1996) 1.39
Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12. Genome Res (1998) 1.36
Polymorphisms in the DNA repair gene XRCC1 and breast cancer. Cancer Epidemiol Biomarkers Prev (2001) 1.35
Migration and genetic infrastructure of the Central American Guaymi and their affinities with other tribal groups. Am J Phys Anthropol (1982) 1.35
Assignment of a human DNA-repair gene associated with sister-chromatid exchange to chromosome 19. Mutat Res (1986) 1.34
An evaluation of human sperm as indicators of chemically induced alterations of spermatogenic function. A report of the U.S. Environmental Protection Agency Gene-Tox Program. Mutat Res (1983) 1.32
Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1. Nucleic Acids Res (1998) 1.32
Amino acid sequence and posttranslational modifications of human factor VIIa from plasma and transfected baby hamster kidney cells. Biochemistry (1988) 1.32
EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins. Genomics (2000) 1.31
Hypersensitivity to mutation and sister-chromatid-exchange induction in CHO cell mutants defective in incising DNA containing UV lesions. Somatic Cell Genet (1982) 1.30
DNA-mediated transfer of a human DNA repair gene that controls sister chromatid exchange. Mol Cell Biol (1985) 1.27
Mycobacterial contamination of metalworking fluids: involvement of a possible new taxon of rapidly growing mycobacteria. AIHAJ (2000) 1.27
Identification of variants of CYP3A4 and characterization of their abilities to metabolize testosterone and chlorpyrifos. J Pharmacol Exp Ther (2001) 1.26
Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta. J Biol Chem (1991) 1.25
Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate. Genomics (1998) 1.24
Laparoscopic excision of a mesenteric cyst. J Laparoendosc Surg (1993) 1.23
Secretion of glucagon-like peptide-1 in patients with type 2 diabetes mellitus: systematic review and meta-analyses of clinical studies. Diabetologia (2013) 1.22
Frequency of enzyme deficiency variants in erythrocytes of newborn infants. Proc Natl Acad Sci U S A (1981) 1.22
Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients. Gut (2002) 1.22
A double blind randomized cross over trial comparing rate of decortication and efficacy of intrapleural instillation of alteplase vs placebo in patients with empyemas and complicated parapneumonic effusions. Respir Med (2012) 1.19
Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids. Somat Cell Mol Genet (1987) 1.19
Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers. Genomics (1993) 1.17
Studies of metaphase and interphase chromosomes using fluorescence in situ hybridization. Cold Spring Harb Symp Quant Biol (1993) 1.17
Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19. Cytogenet Cell Genet (1989) 1.16
Tryptic peptide analysis of normal and mutant forms of hypoxanthine phosphoribosyltransferase from HeLa cells. Proc Natl Acad Sci U S A (1977) 1.16
The DNA content of micronuclei induced in mouse bone marrow by gamma-irradiation: evidence that micronuclei arise from acentric chromosomal fragments. Mutat Res (1977) 1.15
DNA-strand breaks associated with halogenated pyrimidine incorporation. Mutat Res (1984) 1.15
Genetic variability in susceptibility and response to toxicants. Toxicol Lett (2001) 1.15
Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene. Genomics (1998) 1.14
Immune complexes in uveitis. Am J Ophthalmol (1979) 1.14
The amino acid sequence of pancreatic spasmolytic polypeptide. Biochim Biophys Acta (1985) 1.14
Rhizomucor miehei triglyceride lipase is synthesized as a precursor. Lipids (1988) 1.13
Patient accuracy of reporting on hereditary non-polyposis colorectal cancer-related malignancy in family members. Br J Surg (2001) 1.12
Physical and genetic mapping of novel microsatellite polymorphisms on human chromosome 19. Genomics (1996) 1.12
A slice chamber for intracellular and extracellular recording during continuous perfusion. Brain Res Bull (1983) 1.11
Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes. Genomics (1996) 1.11
Characterization of human and rat intestinal trefoil factor produced in yeast. Biochemistry (1995) 1.11
The DNA-based human karyotype. Cytometry (1984) 1.11
Patients with schizophrenia treated with aripiprazole, a multicentre naturalistic study. Acta Psychiatr Scand (2006) 1.11
Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints. Genome Res (2000) 1.10
Erythrocyte enzyme deficiencies assessed with a miniature centrifugal analyzer. Clin Chem (1979) 1.10
Production and processing of erythropoietin receptor transcripts in brain. Brain Res Mol Brain Res (2000) 1.09
Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants. Pediatr Res (1982) 1.09
Equivalence lack in digoxin plasma levels. JAMA (1973) 1.09
Regulation of glucagon secretion by incretins. Diabetes Obes Metab (2011) 1.08
Chinese hamster hypoxanthine-guanine phosphoribosyltransferase. Purification, structural, and catalytic properties. J Biol Chem (1974) 1.08
Nonsurgical treatment of splenic hemorrhage in an adult with infectious mononucleosis. Case report and review. Am J Med (1986) 1.07
Frequency of XY sperm increases with age in fathers of boys with Klinefelter syndrome. Am J Hum Genet (2001) 1.07
CLH-3, a ClC-2 anion channel ortholog activated during meiotic maturation in C. elegans oocytes. Curr Biol (2001) 1.07
New nomenclature for the human tissue kallikrein gene family. Clin Chem (2000) 1.06
Cytogenetic characterization of the ionizing radiation-sensitive Chinese hamster mutant irs1. Mutat Res (1991) 1.05
High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils. J Mol Biol (1998) 1.05
Hominoid triosephosphate isomerase: characterization of the major cell proliferation specific isozyme. Mol Cell Biochem (1986) 1.05
Human chromosome isolation from short-term lymphocyte culture for flow cytometry. Nature (1981) 1.04
An enzymatically inactive variant of human lactate dehydrogenase-LDHBGUA-1. Study of subunit interaction. Biochim Biophys Acta (1982) 1.04
Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19. Genomics (1998) 1.04