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5 documents found
1: Title: Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction.
Authors: Yoshino, Satoshi, et.al. .
Journal: Journal of the American Heart Association (J Am Heart Assoc), Vol. 5 (4): e002544, 2016 .
Snippet: SNPs significantly associated with coronary epicardial endothelial dysfunction were ADORA1, KCNQ1, and DNAJC4 in the whole cohort, LPA, MYBPH, ADORA3, and PON1 in women and KIF6 and NFKB1 in men (P<0.01).
Affiliation: Cardiovascular Medicine and Hypertension, Kagoshima University Hospital, Sakuragaoka, Kagoshima, Japan. Cardiovascular Diseases and Internal Medicine, Mayo Clinic and College of Medicine, Rochester, MN. Biomedical Statistics and Informatics, Mayo Clinic and College of Medicine, Rochester, MN. Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine, Aoba-ku, Sendai, Japan. Genomics Shared Resource, Mayo Clinic and College of Medicine, Rochester, MN. Nephrology and Internal Medicine, Mayo Clinic and College of Medicine, Rochester, MN. Cardiovascular Diseases and Internal Medicine, Mayo Clinic and College of Medicine, Rochester, MN lerman.amir@mayo.edu. .
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2: Title: Dexamethasone acutely regulates endocrine parameters in stallions and subsequently affects gene expression in testicular germ cells.
Authors: Ing, N H, et.al. .
Journal: Animal reproduction science (Anim Reprod Sci), Vol. 152, 2015 .
Snippet: Functional genomic analyses of the testes revealed that, of eight gene products analyzed, dexamethasone depressed concentrations of heat shock protein DNAJC4 and sperm-specific calcium channel CATSPER1 mRNAs by more than 60%.
Affiliation: Department of Animal Science, Texas A&M AgriLife Research, Texas A&M University, College Station, TX 77843-2471, United States. Electronic address: ning@cvm.tamu.edu. Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biosciences, Texas A&M University, College Station, TX 77843-2471, United States. Department of Animal Science, Texas A&M AgriLife Research, Texas A&M University, College Station, TX 77843-2471, United States. Department of Veterinary Physiology and Pharmacology, College of Veterinary Medicine and Biosciences, Texas A&M University, College Station, TX 77843-2471, United States. .
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3: Title: Dense spermatozoa in stallion ejaculates contain lower concentrations of mRNAs encoding the sperm specific calcium channel 1, ornithine decarboxylase antizyme 3, aromatase, and estrogen receptor alpha than less dense spermatozoa.
Authors: Ing, N H, et.al. .
Journal: Theriogenology, Vol. 82 (2): 347-53, 2014 .
Snippet: In contrast, concentrations of three other mRNAs, encoding PRM1 and heat shock proteins HSPA8 and DNAJC4, were not different (P > 0.1).
Affiliation: Department of Animal Science, Texas A&M AgriLife Research, Texas A&M University, College Station, Texas, USA. Electronic address: ning@cvm.tamu.edu. Department of Animal Science, Texas A&M AgriLife Research, Texas A&M University, College Station, Texas, USA. Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biosciences, Texas A&M University, College Station, Texas, USA. .
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4: Title: Core temperature correlates with expression of selected stress and immunomodulatory genes in febrile patients with sepsis and noninfectious SIRS.
Authors: Sonna, Larry A, et.al. .
Journal: Cell stress & chaperones (Cell Stress Chaperones), Vol. 15 (1): 55-66, 2010 .
Snippet: Twelve sequences demonstrated temperature-dependent responses that differed significantly between patients with sepsis and noninfectious SIRS: CXCL-13; heat shock proteins DNAJB12 and DNAJC4; the F11 receptor; folate hydrolase 1; HSF-2; HSP 70 proteins HSPA1A, HSPA1B, and HSPA1L; interleukin 8; lipopolysaccharide binding protein; and prostaglandin E synthase.
Affiliation: University of Maryland School of Medicine, Baltimore, MD 21201, USA. larry_sonna@hotmail.com .
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5: Title: Characterisation of a new human and murine member of the DnaJ family of proteins.
Authors: Silins, G, et.al. .
Journal: Biochemical and biophysical research communications (Biochem Bioph Res Co), Vol. 243 (1): 273-6, 1998 .
Snippet: We report the characterisation of a human gene, designated MCG18 (multiple endocrine neoplasia type 1 candidate gene 18), that encodes a new member of the DnaJ family of proteins.
Affiliation: Queensland Cancer Fund Research Unit, Joint Experimental Oncology Program, Queensland Institute of Medical Research, Herston, Australia. gintS@qimr.edu.au .
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