Published in Mamm Genome on August 01, 2001
Ipr1 gene mediates innate immunity to tuberculosis. Nature (2005) 4.53
Identification of a missense mutation in the bovine ABCG2 gene with a major effect on the QTL on chromosome 6 affecting milk yield and composition in Holstein cattle. Genome Res (2005) 2.51
Gene expression profiling of aging in multiple mouse strains: identification of aging biomarkers and impact of dietary antioxidants. Aging Cell (2009) 1.44
On the origin and evolution of vertebrate olfactory receptor genes: comparative genome analysis among 23 chordate species. Genome Biol Evol (2009) 1.09
Sinusoidal obstruction syndrome (hepatic veno-occlusive disease). J Clin Exp Hepatol (2014) 1.04
A multi-megabase copy number gain causes maternal transmission ratio distortion on mouse chromosome 2. PLoS Genet (2015) 0.93
Gene expression profile of mouse white adipose tissue during inflammatory stress: age-dependent upregulation of major procoagulant factors. Aging Cell (2013) 0.93
New members of the neurexin superfamily: multiple rodent homologues of the human CASPR5 gene. Mamm Genome (2006) 0.83
Pollen Killer Gene S35 Function Requires Interaction with an Activator That Maps Close to S24, Another Pollen Killer Gene in Rice. G3 (Bethesda) (2016) 0.76
Chromatin preferences of the perichromosomal layer constituent pKi-67. Chromosome Res (2002) 0.75
SP110b Controls Host Immunity and Susceptibility to Tuberculosis. Am J Respir Crit Care Med (2016) 0.75
Variability of the chromosome 1 HSR of "Asian" type in the wild mouse (Mus musculus). Dokl Biol Sci (2007) 0.75
Initial sequencing and analysis of the human genome. Nature (2001) 212.86
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science (2009) 13.45
Comparative analyses of multi-species sequences from targeted genomic regions. Nature (2003) 13.31
A physical map of the human genome. Nature (2001) 12.39
Ligation-independent cloning of PCR products (LIC-PCR). Nucleic Acids Res (1990) 12.16
Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature (2001) 10.96
The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene. Cell (1999) 7.99
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments. Nat Genet (1994) 5.34
Bacterial artificial chromosome libraries for mouse sequencing and functional analysis. Genome Res (2000) 5.13
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet (1998) 4.38
Stable propagation of cosmid sized human DNA inserts in an F factor based vector. Nucleic Acids Res (1992) 3.97
A bacterial artificial chromosome library for sequencing the complete human genome. Genome Res (2001) 3.81
An improved approach for construction of bacterial artificial chromosome libraries. Genomics (1998) 3.65
Genome evolution. Global methylation in eutherian hybrids. Nature (1999) 3.61
A BAC-based physical map of the major autosomes of Drosophila melanogaster. Science (2000) 3.51
Positional cloning of the mouse saccharin preference (Sac) locus. Chem Senses (2001) 2.75
A modular, positive selection bacterial artificial chromosome vector with multiple cloning sites. Genomics (1999) 2.17
The MHC haplotype project: a resource for HLA-linked association studies. Tissue Antigens (2002) 2.16
TTAGG telomeric repeats in chromosomes of some insects and other arthropods. Chromosome Res (1999) 2.06
In vitro cleavage and joining at the viral origin of replication by the replication initiator protein of tomato yellow leaf curl virus. Proc Natl Acad Sci U S A (1995) 1.93
A high-resolution, fluorescence-based, semiautomated method for DNA fingerprinting. Genomics (1989) 1.75
Robertsonian metacentrics in the mouse. Chromosoma (1976) 1.72
Fertile XX- and XY-type females in the wood lemming Myopus schisticolor. Nature (1976) 1.66
Construction and characterization of a new bovine bacterial artificial chromosome library with 10 genome-equivalent coverage. Mamm Genome (2000) 1.65
The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X. Nature (2001) 1.63
Rapid cloning and characterization of new chromosome 10 DNA markers by Alu element-mediated PCR. Genomics (1990) 1.59
Molecular isolation and characterization of an expressed gene from the human Y chromosome. Hum Mol Genet (1992) 1.56
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients. J Med Genet (2004) 1.50
New lessons for combinatorial biosynthesis from myxobacteria. The myxothiazol biosynthetic gene cluster of Stigmatella aurantiaca DW4/3-1. J Biol Chem (1999) 1.49
Adenovirus isolates from urine of patients with acquired immunodeficiency syndrome. Lancet (1983) 1.45
Cloning and characterization of MN1, a gene from chromosome 22q11, which is disrupted by a balanced translocation in a meningioma. Oncogene (1995) 1.44
A new type of erythrokeratoderma. Br J Dermatol (2005) 1.43
The chondramides: cytostatic agents from myxobacteria acting on the actin cytoskeleton. J Natl Cancer Inst (1998) 1.42
Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis. Ann Neurol (2001) 1.42
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. Hum Mol Genet (1996) 1.42
Robertsonian chromosomal variation and identification of metacentric chromosomes in feral mice. Chromosoma (1972) 1.41
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation. J Med Genet (2007) 1.40
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry. Br J Dermatol (2012) 1.39
Base substitutions, frameshifts, and small deletions constitute ionizing radiation-induced point mutations in mammalian cells. Proc Natl Acad Sci U S A (1988) 1.39
Pachytene mapping in the female silkworm, Bombyx mori L. (Lepidoptera). Chromosoma (1976) 1.31
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation. J Med Genet (2004) 1.30
Construction and characterization of an eightfold redundant dog genomic bacterial artificial chromosome library. Genomics (1999) 1.30
Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products. PCR Methods Appl (1994) 1.29
Molecular evidence for the rapid propagation of mouse t haplotypes from a single, recent, ancestral chromosome. Mol Biol Evol (1987) 1.27
Rescue of unstable cosmids by in vitro packaging. Nucleic Acids Res (1991) 1.27
Meiotic chromosomes and stages of sex chromosome evolution in fish: zebrafish, platyfish and guppy. Chromosome Res (2001) 1.27
A missense mutation in the type II hair keratin hHb3 is associated with monilethrix. J Med Genet (2005) 1.26
Novel features in a combined polyketide synthase/non-ribosomal peptide synthetase: the myxalamid biosynthetic gene cluster of the myxobacterium Stigmatella aurantiaca Sga15. Chem Biol (2001) 1.26
A porcine BAC library with tenfold genome coverage: a resource for physical and genetic map integration. Mamm Genome (2001) 1.26
Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome library. Genomics (1998) 1.22
Two binding sites of inhibitors in NADH: ubiquinone oxidoreductase (complex I). Relationship of one site with the ubiquinone-binding site of bacterial glucose:ubiquinone oxidoreductase. Eur J Biochem (1994) 1.21
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. Am J Med Genet A (2009) 1.21
A genomic region encompassing a cluster of olfactory receptor genes and a myosin light chain kinase (MYLK) gene is duplicated on human chromosome regions 3q13-q21 and 3p13. Genomics (1999) 1.19
Using a pericentromeric interspersed repeat to recapitulate the phylogeny and expansion of human centromeric segmental duplications. Mol Biol Evol (2003) 1.18
The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements. Genomics (1999) 1.17
The structural organization of the human skeletal muscle ryanodine receptor (RYR1) gene. Genomics (1996) 1.17
Histocompatibility-2 system in wild mice. X. Frequencies of H-2 and Ia antigens in wild mice from Europe and Africa. J Immunol (1980) 1.16
Genomic sequence of a 320-kb segment of the Z chromosome of Bombyx mori containing a kettin ortholog. Mol Genet Genomics (2003) 1.15
A novel missense mutation in GJB2 disturbs gap junction protein transport and causes focal palmoplantar keratoderma with deafness. J Med Genet (2007) 1.13
Human ribosomal RNA gene cluster: identification of the proximal end containing a novel tandem repeat sequence. Genomics (1995) 1.13
A cross-cultural study of animal fears. Behav Res Ther (1998) 1.12
An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region. Genomics (1996) 1.11
Dual Alu polymerase chain reaction primers and conditions for isolation of human chromosome painting probes from hybrid cells. Cancer Genet Cytogenet (1993) 1.11
In vitro reconstitution of the myxochelin biosynthetic machinery of Stigmatella aurantiaca Sg a15: Biochemical characterization of a reductive release mechanism from nonribosomal peptide synthetases. Proc Natl Acad Sci U S A (2001) 1.10
The myxochelin iron transport regulon of the myxobacterium Stigmatella aurantiaca Sg a15. Eur J Biochem (2000) 1.09
Evolution of a long-range repeat family in chromosome 1 of the genus Mus. Mamm Genome (1993) 1.08
The t(14;21)(q11.2;q22) chromosomal translocation associated with T-cell acute lymphoblastic leukemia activates the BHLHB1 gene. Proc Natl Acad Sci U S A (2000) 1.08
Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q. Genomics (1992) 1.06
The organization of the human immunoglobulin lambda gene locus. Genome Res (1995) 1.06
Environmental regulation of alcohol metabolism in thermotolerant methylotrophic Bacillus strains. Arch Microbiol (1992) 1.06
Mta, the maternally transmitted antigen, is determined jointly by the chromosomal Hmt and the extrachromosomal Mtf genes. J Exp Med (1986) 1.05
Large-insert BAC/YAC libraries for selective re-isolation of genomic regions by homologous recombination in yeast. Genomics (2001) 1.05
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma. Am J Med Genet A (2005) 1.05
Cosmid assembly and anchoring to human chromosome 21. Genomics (1995) 1.05
Robertsonian karyotype variation in wild house mice from Rhaeto-Lombardia. Cytogenet Cell Genet (1982) 1.05
Down's syndrome in the male. Reproductive pathology and meiotic studies. Hum Genet (1983) 1.03
Murine trisomy: developmental profiles of the embryo, and isolation of trisomic cellular systems. J Exp Zool (1983) 1.03
Expression of the sex determining cascade genes Sex-lethal and doublesex in the phorid fly Megaselia scalaris. Genome (1997) 1.03
Trisomy 16 in the mouse fetus associated with generalized edema and cardiovascular and urinary tract anomalies. Teratology (1982) 1.02
Characterization of a recombinant mouse T haplotype that expresses a dominant lethal maternal effect. Genetics (1984) 1.02
Variable positions of NORs in Mus musculus. Cytogenet Cell Genet (1980) 1.02
The sex-determining gene doublesex in the fly Megaselia scalaris: conserved structure and sex-specific splicing. Genome (2000) 1.01
A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13. Genomics (1997) 1.00
Silent myocardial ischemia as a potential link between lack of premonitoring symptoms and increased risk of cardiac arrest during physical stress. Am J Cardiol (1990) 1.00
Chromosome cores and chromatin at meiotic prophase. Curr Top Dev Biol (1998) 1.00
A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13. Genomics (1997) 0.99
An extra segment in chromosome 1 of wild Mus musculus: a C-band positive homogeneously staining region. Cytogenet Cell Genet (1984) 0.99
Evolution of a 6-200 Mb long-range repeat cluster in the genus Mus. Chromosoma (2001) 0.99
A comparative mapping study of fragile sites in the human and murine genomes. Hum Genet (1987) 0.98