Published in Eur J Biochem on October 01, 1981
Physical change in cytoplasmic messenger ribonucleoproteins in cells treated with inhibitors of mRNA transcription. Mol Cell Biol (1984) 5.44
Monoclonal antibody characterization of the C proteins of heterogeneous nuclear ribonucleoprotein complexes in vertebrate cells. J Cell Biol (1984) 4.18
Characterization of heterogeneous nuclear RNA-protein complexes in vivo with monoclonal antibodies. Mol Cell Biol (1984) 4.11
Isolation of the heterogeneous nuclear RNA-ribonucleoprotein complex (hnRNP): a unique supramolecular assembly. Proc Natl Acad Sci U S A (1984) 3.51
Characterization of the SS-B (La) antigen in adenovirus-infected and uninfected HeLa cells. EMBO J (1983) 1.83
Molecular cloning of cDNA for the nuclear ribonucleoprotein particle C proteins: a conserved gene family. Proc Natl Acad Sci U S A (1986) 1.75
Adenovirus proteins associated with mRNA and hnRNA in infected HeLa cells. J Virol (1987) 1.31
Isolation and characterization of a Xenopus laevis C protein cDNA: structure and expression of a heterogeneous nuclear ribonucleoprotein core protein. Proc Natl Acad Sci U S A (1988) 1.28
Detection of a cellular polypeptide associated with adenovirus-coded VA RNA using in vitro labeling of proteins cross-linked to RNA. Nucleic Acids Res (1982) 1.24
Interaction of mRNA with proteins in vesicular stomatitis virus-infected cells. J Virol (1986) 1.09
Sequence dependent interaction of hnRNP proteins with late adenoviral transcripts. Nucleic Acids Res (1982) 1.02
Non-random localization of ribonucleoprotein (RNP) structures within an adenovirus mRNA precursor. Nucleic Acids Res (1982) 0.99
On the localization and transport of specific adenoviral mRNA-sequences in the late infected HeLa cell. Nucleic Acids Res (1982) 0.96
Antisense-mediated affinity purification of dengue virus ribonucleoprotein complexes from infected cells. Methods (2015) 0.77
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet (1995) 5.58
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus. Cell (1995) 3.72
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease. Hum Mol Genet (1997) 3.56
Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet (1996) 3.53
Mapping of B cell epitopes on small nuclear ribonucleoproteins that react with human autoantibodies as well as with experimentally-induced mouse monoclonal antibodies. J Immunol (1989) 3.13
Results of genetic testing: when confidentiality conflicts with a duty to warn relatives. BMJ (2000) 2.59
Anti-Ro52 antibodies frequently co-occur with anti-Jo-1 antibodies in sera from patients with idiopathic inflammatory myopathy. Clin Exp Immunol (1997) 2.05
Cross-linking of mRNA to proteins by irradiation of intact cells with ultraviolet light. Eur J Biochem (1980) 2.04
The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans. Nat Genet (1993) 1.84
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I. Ann Neurol (1999) 1.72
Adenoviral heterogeneous nuclear RNA is associated with the host nuclear matrix during splicing. J Mol Biol (1982) 1.60
On the association of mRNA with the cytoskeleton in uninfected and adenovirus-infected human KB cells. Exp Cell Res (1981) 1.48
A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2). Nat Genet (1996) 1.47
Further characterization and subcellular localization of Sm and U1 ribonucleoprotein antigens. Eur J Immunol (1985) 1.44
Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects. Nat Genet (2001) 1.30
Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p. Hum Mol Genet (1994) 1.21
Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family. Hum Mol Genet (1996) 1.21
Altered folate and vitamin B12 metabolism in families with spina bifida offspring. QJM (1997) 1.21
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27. Am J Hum Genet (1999) 1.18
Biallelic expression of the H19 and IGF2 genes in human testicular germ cell tumors. J Natl Cancer Inst (1994) 1.17
Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring. J Mol Med (Berl) (1996) 1.17
Alternative splicing pathways exist in the formation of adenoviral late messenger RNAs. J Mol Biol (1983) 1.16
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects. Am J Hum Genet (1993) 1.16
Source of amino acids used for protein synthesis in HeLa cells. Eur J Biochem (1974) 1.16
Structure and function of La and Ro RNPs. Mol Biol Rep (1990) 1.15
Anti-La monoclonal antibodies recognizing epitopes within the RNA-binding domain of the La protein show differential capacities to immunoprecipitate RNA-associated La protein. Eur J Biochem (1995) 1.13
Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. Am J Hum Genet (1993) 1.12
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings. Am J Med Genet (1996) 1.11
A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene. Hum Mol Genet (1994) 1.10
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes. Genomics (2000) 1.08
Characterization of cis-acting signals for nuclear import and retention of the La (SS-B) autoantigen. Exp Cell Res (1996) 1.08
X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3. Am J Med Genet (1999) 1.07
Susceptibility to spina bifida; an association study of five candidate genes. Ann Hum Genet (1998) 1.05
Relationship between extracellular amino acids and protein synthesis in vitro in the rat pancreas. Eur J Biochem (1972) 1.04
Interaction of the La (SS-B) autoantigen with small ribosomal subunits. Eur J Biochem (1996) 1.04
Clinical features and serum antinuclear antibodies in 230 Danish patients with systemic sclerosis. Br J Rheumatol (1998) 1.04
HLA type as a predictor of mixed connective tissue disease differentiation. Ten-year clinical and immunogenetic followup of 46 patients. Arthritis Rheum (1995) 1.00
Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. Neurology (1996) 0.98
Anti-nuclear matrix antibodies in mixed connective tissue disease. Eur J Immunol (1982) 0.97
Association of mRNA and eIF-2 alpha with the cytoskeleton in cells lacking vimentin. Exp Cell Res (1989) 0.96
Detection of autoantibodies in a quantitative immunoassay using recombinant ribonucleoprotein antigens. Clin Exp Immunol (1989) 0.95
The perinuclear factor, a rheumatoid arthritis-specific autoantigen, is not present in keratohyalin granules of cultured buccal mucosa cells. Clin Exp Immunol (1991) 0.95
Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. Brain (1998) 0.95
Autoantibodies to the URNP particles: relationship to clinical diagnosis and nephritis. Clin Exp Immunol (1991) 0.94
Location of the gene causing hyperimmunoglobulinemia D and periodic fever syndrome differs from that for familial Mediterranean fever. International Hyper-IgD Study Group. Hum Genet (1994) 0.94
Synthesis of lens crystallins in Xenopus oocytes as determined by quantitative immunoprecipitation. Eur J Biochem (1978) 0.93
Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2. Br J Cancer (1999) 0.93
Ro (SS-A) and La (SS-B) ribonucleoprotein complexes: structure, function and antigenicity. Ann Med Interne (Paris) (1991) 0.92
A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defects. Hum Mol Genet (2000) 0.91
A large family with multiple epiphyseal dysplasia linked to COL9A2 gene. Am J Med Genet (1998) 0.91
Autoantibody production against the U small nuclear ribonucleoprotein particle proteins E, F and G in patients with connective tissue diseases. Eur J Immunol (1990) 0.91
Screening for autoantibodies to the nucleolar U3- and Th(7-2) ribonucleoproteins in patients' sera using antisense riboprobes. J Immunol Methods (1994) 0.89
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency. Neurology (1999) 0.89
Epitope regions on U1 small nuclear RNA recognized by anti-U1RNA-specific autoantibodies. J Clin Invest (1992) 0.88
Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene. J Invest Dermatol (1994) 0.87
Absence of linkage between familial neural tube defects and PAX3 gene. J Med Genet (1995) 0.87
Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis. Am J Med Genet (1999) 0.87
Characterization of murine monoclonal antibodies against 60-kD Ro/SS-A and La/SS-B autoantigens. Clin Exp Immunol (1995) 0.87
The use of adenovirus-infected HeLa cells for the detection of low titer autoantibodies. J Immunol Methods (1991) 0.87
Glomus tumours and genomic imprinting: influence of inheritance along the paternal or maternal line. Clin Otolaryngol Allied Sci (1997) 0.86
In vivo cross-linking of proteins to mRNA in human cells. Mol Biol Rep (1981) 0.86
Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family. Hum Genet (1995) 0.85
A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome. J Med Genet (1995) 0.85
A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty. J Clin Endocrinol Metab (1999) 0.85
Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood. Hum Genet (1996) 0.85
Improving the polymorphism content of the 3' UTR of the human IGF2R gene. Hum Mol Genet (1992) 0.84
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida. J Med Genet (1996) 0.84
Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins. Proc Natl Acad Sci U S A (1998) 0.84
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies. Am J Med Genet (1994) 0.84
Autoantibodies against small nucleolar ribonucleoprotein complexes and their clinical associations. Clin Exp Immunol (2002) 0.83
A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28. Am J Med Genet (1996) 0.82
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family. Hum Genet (1994) 0.81
Post-translational assembly of lens alpha-crystallin in the reticulocyte lysate and in Xenopus laevis oocytes. Eur J Biochem (1978) 0.81
Prevalence and characteristics of anti-56K/annexin XI autoantibodies in systemic autoimmune diseases. J Rheumatol (1995) 0.81
Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X). Hum Mutat (1998) 0.81
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. Eur J Hum Genet (1999) 0.81
Tryptophan replacement in the C-terminal octapeptide of CCK-PZ. Syntheses of six peptide analogues bearing tryptophan congeners. Int J Pept Protein Res (1980) 0.80
Characterization of poly(A)-protein complexes isolated from free and membrane-bound polyribosomes of Ehrlich ascites tumor cells. Mol Biol Rep (1976) 0.79
A mutation in COL9A2 causes multiple epiphyseal dysplasia (EDM2). Ann N Y Acad Sci (1996) 0.78
An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1. J Invest Dermatol (1998) 0.78
X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region. Am J Med Genet (1999) 0.78
A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region. J Med Genet (1999) 0.78
Regulation and expression of the murine PMP22 gene. Mamm Genome (1999) 0.78
Marker antibodies in scleroderma and polymyositis: clinical associations. Clin Rheumatol (1989) 0.77
SKALP/elafin gene polymorphisms are not associated with pustular forms of psoriasis. Clin Genet (1998) 0.77
EcoRI RFLP at the creatine kinase-brain type gene locus (CKBB, chromosome 14). Nucleic Acids Res (1987) 0.77
Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa. J Invest Dermatol (1994) 0.77
Transcriptome analysis of peripheral blood mononuclear cells in human subjects following a 36 h fast provides evidence of effects on genes regulating inflammation, apoptosis and energy metabolism. Genes Nutr (2014) 0.77
A model for the excision of introns 1 and 2 from adenoviral major late pre-messenger RNAs. J Mol Biol (1984) 0.76
Cloning and characterization of two processed pseudogenes and the cDNA for the murine U1 snRNP-specific protein C. Gene (1997) 0.76
Adenovirus infection induces loss of HLA class I and CD3 antigens, but does not induce cell surface presentation of the La (SS-B) autoantigen. Clin Exp Immunol (1994) 0.75
Clustering of anophthalmia and microphthalmia. No clustering has been found-but a link seems to exist with population density. BMJ (1998) 0.75
Antibodies to soluble and insoluble nuclear antigens in systemic diseases. Clin Rheumatol (1987) 0.75
Proteins present on polyadenylic acid segments of messenger ribonucleic acid in Ehrlich ascites-tumour cells [proceedings]. Biochem Soc Trans (1977) 0.75
Expression of genes involved in lipid metabolism in men with impaired glucose tolerance: impact of insulin stimulation and weight loss. J Nutrigenet Nutrigenomics (2010) 0.75
The AIDS combat: a survey. Biomed Pharmacother (1986) 0.75
Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV. Eur J Pediatr (1997) 0.75