Search Results - (Author, Cooperation:N. J. Cox)
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1S. Smemo ; J. J. Tena ; K. H. Kim ; E. R. Gamazon ; N. J. Sakabe ; C. Gomez-Marin ; I. Aneas ; F. L. Credidio ; D. R. Sobreira ; N. F. Wasserman ; J. H. Lee ; V. Puviindran ; D. Tam ; M. Shen ; J. E. Son ; N. A. Vakili ; H. K. Sung ; S. Naranjo ; R. D. Acemel ; M. Manzanares ; A. Nagy ; N. J. Cox ; C. C. Hui ; J. L. Gomez-Skarmeta ; M. A. Nobrega
Nature Publishing Group (NPG)
Published 2014Staff ViewPublication Date: 2014-03-22Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Adipose Tissue/metabolism ; Animals ; Basal Metabolism/genetics ; Body Mass Index ; Body Weight/genetics ; Brain/metabolism ; Diabetes Mellitus, Type 2/genetics ; Diet ; Genes, Dominant/genetics ; Homeodomain Proteins/*genetics/metabolism ; Humans ; Hypothalamus/metabolism ; Introns/*genetics ; Male ; Mice ; Mixed Function Oxygenases/*genetics ; Obesity/*genetics ; Oxo-Acid-Lyases/*genetics ; Phenotype ; Polymorphism, Single Nucleotide/genetics ; Promoter Regions, Genetic/genetics ; Proteins/*genetics ; Thinness/genetics ; Transcription Factors/deficiency/*genetics/metabolism ; Zebrafish/embryology/geneticsPublished by: -
2T. Bedford ; S. Riley ; I. G. Barr ; S. Broor ; M. Chadha ; N. J. Cox ; R. S. Daniels ; C. P. Gunasekaran ; A. C. Hurt ; A. Kelso ; A. Klimov ; N. S. Lewis ; X. Li ; J. W. McCauley ; T. Odagiri ; V. Potdar ; A. Rambaut ; Y. Shu ; E. Skepner ; D. J. Smith ; M. A. Suchard ; M. Tashiro ; D. Wang ; X. Xu ; P. Lemey ; C. A. Russell
Nature Publishing Group (NPG)
Published 2015Staff ViewPublication Date: 2015-06-09Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Age Factors ; *Antigenic Variation ; Global Health ; Humans ; Influenza A virus/classification/*genetics ; Influenza B virus/classification/*genetics ; Influenza, Human/*epidemiology/*virology ; Phylogeny ; Phylogeography ; SeasonsPublished by: -
3D. G. MacArthur ; T. A. Manolio ; D. P. Dimmock ; H. L. Rehm ; J. Shendure ; G. R. Abecasis ; D. R. Adams ; R. B. Altman ; S. E. Antonarakis ; E. A. Ashley ; J. C. Barrett ; L. G. Biesecker ; D. F. Conrad ; G. M. Cooper ; N. J. Cox ; M. J. Daly ; M. B. Gerstein ; D. B. Goldstein ; J. N. Hirschhorn ; S. M. Leal ; L. A. Pennacchio ; J. A. Stamatoyannopoulos ; S. R. Sunyaev ; D. Valle ; B. F. Voight ; W. Winckler ; C. Gunter
Nature Publishing Group (NPG)
Published 2014Staff ViewPublication Date: 2014-04-25Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: *Disease ; False Positive Reactions ; Genes/genetics ; Genetic Predisposition to Disease/*genetics ; Genetic Variation/*genetics ; *Guidelines as Topic ; Humans ; Information Dissemination ; Publishing ; Reproducibility of Results ; Research Design ; Translational Medical Research/standardsPublished by: -
4R. A. Fouchier ; A. Garcia-Sastre ; Y. Kawaoka ; W. S. Barclay ; N. M. Bouvier ; I. H. Brown ; I. Capua ; H. Chen ; R. W. Compans ; R. B. Couch ; N. J. Cox ; P. C. Doherty ; R. O. Donis ; H. Feldmann ; Y. Guan ; J. M. Katz ; O. I. Kiselev ; H. D. Klenk ; G. Kobinger ; J. Liu ; X. Liu ; A. Lowen ; T. C. Mettenleiter ; A. D. Osterhaus ; P. Palese ; J. S. Peiris ; D. R. Perez ; J. A. Richt ; S. Schultz-Cherry ; J. Steel ; K. Subbarao ; D. E. Swayne ; T. Takimoto ; M. Tashiro ; J. K. Taubenberger ; P. G. Thomas ; R. A. Tripp ; T. M. Tumpey ; R. J. Webby ; R. G. Webster
American Association for the Advancement of Science (AAAS)
Published 2013Staff ViewPublication Date: 2013-01-25Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Biomedical Research/*trends ; Birds ; Humans ; *Influenza A Virus, H5N1 Subtype ; Influenza in Birds/*transmission/*virology ; Influenza, Human/*transmission/*virologyPublished by: -
5Staff View
Publication Date: 2013-08-30Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Air ; Antarctic Regions ; Climate Change/*statistics & numerical data ; *Ice Cover ; Pacific Ocean ; Seasons ; Seawater/analysis ; Temperature ; Time FactorsPublished by: -
6R. A. Fouchier ; A. Garcia-Sastre ; Y. Kawaoka ; W. S. Barclay ; N. M. Bouvier ; I. H. Brown ; I. Capua ; H. Chen ; R. W. Compans ; R. B. Couch ; N. J. Cox ; P. C. Doherty ; R. O. Donis ; H. Feldmann ; Y. Guan ; J. Katz ; H. D. Klenk ; G. Kobinger ; J. Liu ; X. Liu ; A. Lowen ; T. C. Mettenleiter ; A. D. Osterhaus ; P. Palese ; J. S. Peiris ; D. R. Perez ; J. A. Richt ; S. Schultz-Cherry ; J. Steel ; K. Subbarao ; D. E. Swayne ; T. Takimoto ; M. Tashiro ; J. K. Taubenberger ; P. G. Thomas ; R. A. Tripp ; T. M. Tumpey ; R. J. Webby ; R. G. Webster
American Association for the Advancement of Science (AAAS)
Published 2012Staff ViewPublication Date: 2012-01-28Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; *Biomedical Research ; Disease Models, Animal ; Ferrets ; Humans ; *Influenza A Virus, H5N1 Subtype/pathogenicity ; Influenza, Human/transmission/virology ; Orthomyxoviridae Infections/*transmission/virologyPublished by: -
7Bastarache, L., Hughey, J. J., Hebbring, S., Marlo, J., Zhao, W., Ho, W. T., Van Driest, S. L., McGregor, T. L., Mosley, J. D., Wells, Q. S., Temple, M., Ramirez, A. H., Carroll, R., Osterman, T., Edwards, T., Ruderfer, D., Velez Edwards, D. R., Hamid, R., Cogan, J., Glazer, A., Wei, W.-Q., Feng, Q., Brilliant, M., Zhao, Z. J., Cox, N. J., Roden, D. M., Denny, J. C.
American Association for the Advancement of Science (AAAS)
Published 2018Staff ViewPublication Date: 2018-03-16Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyGeosciencesComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: GeneticsPublished by: -
8Staff View
ISSN: 1432-0428Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: -
9Stirling, B. ; Cox, N. J. ; Bell, G. I. ; Hanis, C. L. ; Spielman, R. S. ; Concannon, P.
Springer
Published 1995Staff ViewISSN: 1432-0428Keywords: Sulphonylurea receptor ; non-insulin-dependent diabetes mellitus ; genetics ; polymorphism ; linkage mappingSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Summary The high affinity receptor for sulphonylureas, expressed on the beta cells of the pancreas, plays a crucial role in the control of insulin secretion. Mutations in the cytoplasmic domain of the sulphonylurea receptor (SUR) gene that disrupt the regulation of insulin secretion have been previously described. In the present study, the potential role of genetic variation in the SUR gene has been investigated in non-insulin-dependent diabetes mellitus (NIDDM) through linkage studies with microsatellite markers tightly linked to the SUR gene. The microsatellite markers were typed in 346 Mexican-American NIDDM affected sib pairs derived from 176 families and an additional 110 ethnically and geographically matched control subjects. No evidence of linkage, based on allele sharing, or association based on allele frequencies in patients and control subjects, for any microsatellite marker and NIDDM was observed in this population. These results suggest that genetic variation in the SUR gene does not play a major role in susceptibility to NIDDM in the Mexican-American population.Type of Medium: Electronic ResourceURL: -
10Yamagata, K. ; Takeda, J. ; Menzel, S. ; Chen, X. ; Eng, S. ; Lim, L. R. ; Concannon, P. ; Hanis, C. L. ; Spielman, R. S. ; Cox, N. J. ; Bell, G. I.
Springer
Published 1996Staff ViewISSN: 1432-0428Keywords: Keywords Diabetes mellitus ; insulin resistance ; genetics ; linkage analysis.Source: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Summary The expansion of trinucleotide repeats has been associated with late-onset neurodegenerative disorders. Although the genes harbouring the triplet expansions may be widely expressed, the pathological expression of these diseases is restricted to specific tissues. Non-insulin-dependent diabetes mellitus (NIDDM) shares several features with diseases resulting from such dynamic mutations including late-onset and specific but limited sites of tissue pathology – muscle, fat, liver and insulin-secreting pancreatic beta cells. In order to examine the contribution of genes containing polymorphic CAG/CTG repeats to the development of NIDDM, we screened an adult human skeletal muscle cDNA library for expressed sequences containing tandem repeats of CAG and/or CTG. Ten different loci with polymorphic CAG/CTG repeats were identified, of which seven had a heterozygosity greater than 0.20. There was no evidence for linkage between these seven loci and NIDDM in a group of affected Mexican-American sib pairs. Nor was there a significant difference in the distribution of alleles between Caucasian patients with NIDDM and normal healthy control subjects or evidence for repeat expansion in diabetic subjects. Thus, muscle genes with polymorphic CAG/CTG repeats do not appear to play a significant role in the development of NIDDM. [Diabetologia (1996) 39: 725–730]Type of Medium: Electronic ResourceURL: -
11Yamagata, K. ; Takeda, J. ; Menzel, S. ; Chen, X. ; Eng, S. ; Lim, L. R. ; Concannon, P. ; Hanis, C. L. ; Spielman, R. S. ; Cox, N. J. ; Bell, G. I.
Springer
Published 1996Staff ViewISSN: 1432-0428Keywords: Diabetes mellitus ; insulin resistance ; genetics ; linkage analysisSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Summary The expansion of trinucleotide repeats has been associated with late-onset neurodegenerative disorders. Although the genes harbouring the triplet expansions may be widely expressed, the pathological expression of these diseases is restricted to specific tissues. Non-insulin-dependent diabetes mellitus (NIDDM) shares several features with diseases resulting from such dynamic mutations including late-onset and specific but limited sites of tissue pathology — muscle, fat, liver and insulin-secreting pancreatic beta cells. In order to examine the contribution of genes containing polymorphic CAG/CTG repeats to the development of NIDDM, we screened an adult human skeletal muscle cDNA library for expressed sequences containing tandem repeats of CAG and/or CTG. Ten different loci with polymorphic CAG/CTG repeats were identified, of which seven had a heterozygosity greater than 0.20. There was no evidence for linkage between these seven loci and NIDDM in a group of affected Mexican-American sib pairs. Nor was there a significant difference in the distribution of alleles between Caucasian patients with NIDDM and normal healthy control subjects or evidence for repeat expansion in diabetic subjects. Thus, muscle genes with polymorphic CAG/CTG repeats do not appear to play a significant role in the development of NIDDM.Type of Medium: Electronic ResourceURL: -
12Hara, M. ; Wang, X. ; Paz, V. P. ; Cox, N. J. ; Iwasaki, N. ; Ogata, M. ; Iwamoto, Y. ; Bell, G. I.
Springer
Published 2000Staff ViewISSN: 1432-0428Keywords: Keywords Maturity-onset diabetes of the young ; MODY ; transcription factor ; nuclear receptor ; HNF-4γ ; diabetes mellitus ; insulin ; genetics ; mutation.Source: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract Aims/hypothesis. Mutations in the transcription factor hepatocyte nuclear factor (HNF)-4α are the cause of one form of maturity-onset diabetes of the young, MODY1. The HNF-4γ is structurally related to HNF-4α and is expressed together with HNF-4α in pancreatic islets. We therefore tested the hypothesis that genetic variation in the HNF-4γ gene (HNF4G) is associated with MODY in Japanese subjects. Methods. We screened the protein coding region of HNF4G (exons 3–11) for mutations in 57 unrelated Japanese subjects with MODY by amplifying each exon and adjacent intron region using the polymerase chain reaction (PCR) and specific primers and then directly sequencing the PCR products. The frequency of each variant was compared between patients with MODY and a group of non-diabetic subjects. Results. We found ten sequence variants, two of these were located in exons: exon 6, a silent substitution in codon 144, c.432A/G and exon 7, a G-to-A substitution in codon 190 (c.570G/A) resulting in a conservative Met-to-Ile substitution (M/I190) in the putative ligand-binding region of HNF-4γ protein. The remaining eight variants were located in introns. There was no significant difference in the frequency of these polymorphisms between subjects with MODY and non-diabetic control subjects. Conclusion/interpretation. Genetic variation in the coding region of HNF4G is unlikely to be a major cause of MODY in Japanese people. [Diabetologia (2000) 43: 1064–1069]Type of Medium: Electronic ResourceURL: -
13Staff View
ISSN: 1435-4373Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: -
14Staff View
ISSN: 1435-4373Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: