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  • 1-10 ل  21 نتائج ل ""Receptors, Cytoplasmic and Nuclear""
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Academic Journal

The NR4A nuclear receptor family in eosinophils.

  • Authors : Hashida R; Genox Research Inc., Bunkyo, Tokyo, 112-8088, Japan. .; Ohkura N

Subjects: Eosinophils/Eosinophils/Eosinophils/*metabolism ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*antagonists & inhibitors ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*metabolism

  • Source: Journal of human genetics [J Hum Genet] 2007; Vol. 52 (1), pp. 13-20. Date of Electronic Publication: 2006 Nov 10.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortium.

  • Authors : Martino A; Genomic Epidemiology Group, German Cancer Research Center DKFZ, Heidelberg, Germany.; Sainz J

Subjects: Polymorphism, Single Nucleotide*; Multiple Myeloma/Multiple Myeloma/Multiple Myeloma/*genetics ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*metabolism

  • Source: Journal of human genetics [J Hum Genet] 2013 Mar; Vol. 58 (3), pp. 155-9. Date of Electronic Publication: 2013 Jan 10.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter.

  • Authors : Uno Y; Division of Genetic Diagnosis, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.; Sakamoto Y

Subjects: Sequence Deletion*; Asthma/Asthma/Asthma/*genetics ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2003; Vol. 48 (11), pp. 594-7. Date of Electronic Publication: 2003 Oct 29.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation.

  • Authors : Saitsu H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.; Tohyama J

Subjects: Mutation, Missense*; Autistic Disorder/Autistic Disorder/Autistic Disorder/*genetics ; Nuclear Proteins/Nuclear Proteins/Nuclear Proteins/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2014 Oct; Vol. 59 (10), pp. 581-3. Date of Electronic Publication: 2014 Aug 07.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Effect of liver fatty acid binding protein (FABP) T94A missense mutation on plasma lipoprotein responsiveness to treatment with fenofibrate.

  • Authors : Brouillette C; Lipid Research Center, CHUL Research Center, 2705 Laurier Blvd, TR93, Sainte-Foy, QC, Canada, G1V 4G2.; Department of Food Science and Nutrition, Laval University, Laval, QC, Canada.

Subjects: Carrier Proteins/Carrier Proteins/Carrier Proteins/*genetics ; Fenofibrate/Fenofibrate/Fenofibrate/*therapeutic use ; Hyperlipoproteinemias/Hyperlipoproteinemias/Hyperlipoproteinemias/*drug therapy

  • Source: Journal of human genetics [J Hum Genet] 2004; Vol. 49 (8), pp. 424-432. Date of Electronic Publication: 2004 Jul 13.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Association between the PPARalpha-L162V polymorphism and components of the metabolic syndrome.

  • Authors : Robitaille J; Lipid Research Center, CHUQ-CHUL Pavilion, 2705 Laurier Blvd, TR-93, Ste-Foy, QC, Canada, G1V 4G2.; Food Science and Nutrition Department, Laval University, Ste-Foy, QC, Canada.

Subjects: Polymorphism, Genetic*; Cholesterol, LDL/Cholesterol, LDL/Cholesterol, LDL/*genetics ; Hypertriglyceridemia/Hypertriglyceridemia/Hypertriglyceridemia/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2004; Vol. 49 (9), pp. 482-489. Date of Electronic Publication: 2004 Aug 10.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Combined effects of PPARgamma2 P12A and PPARalpha L162V polymorphisms on glucose and insulin homeostasis: the Québec Family Study.

  • Authors : Bossé Y; Lipid Research Center, CHUL Research Center, Laval University, TR-93, 2705 Laurier Blvd., Sainte-Foy, Québec, G1V 4G2, Canada.; Department of Food Sciences and Nutrition, Laval University, Québec, PQ, Canada.

Subjects: Polymorphism, Genetic*; Glucose/Glucose/Glucose/*metabolism ; Insulin/Insulin/Insulin/*metabolism

  • Source: Journal of human genetics [J Hum Genet] 2003; Vol. 48 (12), pp. 614-621. Date of Electronic Publication: 2003 Nov 20.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis.

  • Authors : Ohmori H; Department of Public Health, Asahikawa Medical College, 2-1-1-1 Midorigaoka-higashi, Asahikawa 078-8510, Japan.; Makita Y

Subjects: Glycoproteins/Glycoproteins/Glycoproteins/*genetics ; Osteoporosis, Postmenopausal/Osteoporosis, Postmenopausal/Osteoporosis, Postmenopausal/*genetics ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2002; Vol. 47 (8), pp. 400-6.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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Academic Journal

Identification of polymorphisms in the human SHP1 gene.

  • Authors : Cao H; Blackburn Cardiovascular Genetics Laboratory, Robarts Research Institute, 406-100 Perth Drive, London, ON N6A 5K8, Canada.; Hegele RA

Subjects: Polymorphism, Single Nucleotide*; Lipodystrophy/Lipodystrophy/Lipodystrophy/*genetics ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2002; Vol. 47 (8), pp. 445-7.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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Academic Journal

Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young.

  • Authors : Hara M; Howard Hughes Medical Institute, The University of Chicago, IL 60637, USA. ; Wang X

Subjects: Mutation, Missense*; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*genetics ; Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/Receptors, Cytoplasmic and Nuclear/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2001; Vol. 46 (5), pp. 285-8.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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  • 1-10 ل  21 نتائج ل ""Receptors, Cytoplasmic and Nuclear""