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Language : english Subject : hearing loss, sensorineural Subject : membrane proteins Geographic : united states Filter by : Subject
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Academic Journal

A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.

  • Authors : Walls WD; Molecular Otolaryngology and Renal Research Labs, Department of Otolaryngology-Head and Neck Surgery, University of Iowa Carver College of Medicine, Iowa City, IA, 52242, USA.; Moteki H

Subjects: Genotype* ; Mutation*; Extracellular Matrix Proteins/Extracellular Matrix Proteins/Extracellular Matrix Proteins/*genetics

  • Source: Human genetics [Hum Genet] 2020 Oct; Vol. 139 (10), pp. 1315-1323. Date of Electronic Publication: 2020 May 07.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

PNPLA3 gene polymorphism and overall and cardiovascular mortality in the United States.

  • Authors : Wijarnpreecha K; Department of Internal Medicine, Bassett Medical Center, Cooperstown, New York, USA.; Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Mayo Clinic, Jacksonville, Florida, USA.

Subjects: Genetic Association Studies*; Cardiovascular Diseases/Cardiovascular Diseases/Cardiovascular Diseases/*genetics ; Cardiovascular Diseases/Cardiovascular Diseases/Cardiovascular Diseases/*mortality

  • Source: Journal of gastroenterology and hepatology [J Gastroenterol Hepatol] 2020 Oct; Vol. 35 (10), pp. 1789-1794. Date of Electronic Publication: 2020 Apr 12.Publisher: Blackwell Scientific Publications Country of Publication: Australia NLM ID: 8607909 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Prognostic role of lemur tyrosine kinase-3 germline polymorphisms in adjuvant gastric cancer in Japan and the United States.

  • Authors : Wakatsuki T; Corresponding Author: Heinz-Josef Lenz, Sharon A. Carpenter Laboratory, Division of Medical Oncology, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, 1441 Eastlake Avenue, Los Angeles, CA 90033. .; LaBonte MJ

Subjects: Genetic Association Studies* ; Prognosis*; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics

  • Source: Molecular cancer therapeutics [Mol Cancer Ther] 2013 Oct; Vol. 12 (10), pp. 2261-72. Date of Electronic Publication: 2013 Aug 05.Publisher: American Association for Cancer Research, Inc Country of Publication: United States NLM ID:

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Academic Journal

Association of INSIG2 polymorphism with overweight and LDL in children.

  • Authors : Kaulfers AM; Division of Pediatric Endocrinology, University of South Alabama, Mobile, Alabama, United States of America.; Deka R

Subjects: Polymorphism, Single Nucleotide*; Dyslipidemias/Dyslipidemias/Dyslipidemias/*genetics ; Intracellular Signaling Peptides and Proteins/Intracellular Signaling Peptides and Proteins/Intracellular Signaling Peptides and Proteins/*genetics

  • Source: PloS one [PLoS One] 2015 Jan 21; Vol. 10 (1), pp. e0116340. Date of Electronic Publication: 2015 Jan 21 (Print Publication: 2015).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Association between variants in or near PNPLA3, GCKR, and PPP1R3B with ultrasound-defined steatosis based on data from the third National Health and Nutrition Examination Survey.

Subjects: Polymorphism, Genetic*; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/*genetics ; Fatty Liver/Fatty Liver/Fatty Liver/*genetics

  • Source: Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association [Clin Gastroenterol Publisher: W.B. Saunders for the American Gastroenterological Association Country of Publication: United States

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Academic Journal

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

  • Authors : Gázquez I; Otology and Neurotology Group CTS495, Centro de Genómica e Investigación Oncológica Pfizer-Universidad de Granada-Junta de Andalucía (GENyO), Avda. de la Ilustración, 114, 18014 Granada, Spain.; Moreno A

Subjects: Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Hearing Loss, Sensorineural/Hearing Loss, Sensorineural/Hearing Loss, Sensorineural/*genetics ; Interferon-gamma/Interferon-gamma/Interferon-gamma/*genetics

  • Source: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Publisher: Springer International Country of Publication: Germany NLM ID: 9002937 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Effect of genetic variation in LRRTM3 on risk of Alzheimer disease.

  • Authors : Reitz C; Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, New York, USA. ; Conrad C

Subjects: Alzheimer Disease/Alzheimer Disease/Alzheimer Disease/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics

  • Source: Archives of neurology [Arch Neurol] 2012 Jul; Vol. 69 (7), pp. 894-900.Publisher: American Medical Assn Country of Publication: United States NLM ID: 0372436 Publication Model: Print Cited Medium:

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Academic Journal

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.

  • Authors : Schultz JM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.; Bhatti R

Subjects: Mutation*; Cadherins/Cadherins/Cadherins/*genetics ; Hearing Loss, Sensorineural/Hearing Loss, Sensorineural/Hearing Loss, Sensorineural/*genetics

  • Source: Journal of medical genetics [J Med Genet] 2011 Nov; Vol. 48 (11), pp. 767-75. Date of Electronic Publication: 2011 Sep 22.Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic

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Academic Journal

A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.

  • Authors : Hildebrand MS; Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City, Iowa, USA.; Gandolfo L

Subjects: Genetic Predisposition to Disease* ; Mutation, Missense*; DNA/DNA/DNA/*genetics

  • Source: The Laryngoscope [Laryngoscope] 2010 Dec; Vol. 120 (12), pp. 2489-93.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 8607378 Publication Model: Print Cited Medium:

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  • 1-9 of  9 results for ""Genetic Association Studies""