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Academic Journal

Association of Apolipoprotein A5 Gene Variants with Hyperlipidemic Acute Pancreatitis in Southeastern China.

  • Authors : Li Y; Department of Gastroenterology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, China.; Cai H

Subjects: Apolipoproteins A*/Apolipoproteins A*/Apolipoproteins A*/genetics ; Pancreatitis*/Pancreatitis*/Pancreatitis*/genetics; Humans

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 Sep; Vol. 27 (9), pp. 284-289.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

A Splicing Transcriptome-Wide Association Study Identifies Candidate Altered Splicing for Prostate Cancer Risk.

  • Authors : Sun Y; College of Life Science, Longyan University, Longyan, P.R. China.; Cancer Epidemiology Division, Population Sciences in the Pacific Program, University of Hawaii Cancer Center, University of Hawaii at Manoa, Honolulu, Hawaii, USA.

Subjects: Transcriptome*/Transcriptome*/Transcriptome*/genetics ; Prostatic Neoplasms*/Prostatic Neoplasms*/Prostatic Neoplasms*/genetics; Male

  • Source: Omics : a journal of integrative biology [OMICS] 2023 Aug; Vol. 27 (8), pp. 372-380. Date of Electronic Publication: 2023 Jul 25.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101131135 Publication Model: Print-Electronic

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Academic Journal

Association Between X-Ray Repair Cross-Complementing Group 1 Arg399Gln Polymorphism and Risk of Oral Leukoplakia: A Meta-analysis.

  • Authors : Wang J; Department of Pharmacy, Peking University First Hospital, Xicheng District, Beijing, China.; Zhu C

Subjects: Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/genetics ; Polymorphism, Single Nucleotide*/Polymorphism, Single Nucleotide*/Polymorphism, Single Nucleotide*/genetics; Asian People/Asian People/Asian People/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Dec; Vol. 25 (12), pp. 781-787. Date of Electronic Publication: 2021 Dec Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

C Deletion at the re74650330 Locus of the SLC39A8 Gene (rs74650330) Increases the Risk of Coronary Artery Disease in Individuals with Low-Density Lipoprotein Cholesterol Levels.

  • Authors : Zhang J; Clinical Medical Research Center, Changzhou Key Laboratory of Individualized Diagnosis and Treatment Associated with High Technology Research, The Third Affiliated Hospital of Soochow University, Changzhou, China.; Yu Y

Subjects: Genetic Predisposition to Disease*; Cation Transport Proteins/Cation Transport Proteins/Cation Transport Proteins/*genetics ; Cholesterol, LDL/Cholesterol, LDL/Cholesterol, LDL/*blood

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Oct; Vol. 25 (10), pp. 660-667.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

A Common Variant at 11q23.3 Is Associated with Susceptibility to Atopic Dermatitis in the Han Chinese Population.

  • Authors : Li Y; Department of Dermatology, First Affiliated Hospital, Anhui Medical University, Hefei, China.; Key Laboratory of Dermatology (Anhui Medical University), Ministry of Education, Hefei, China.

Subjects: Genetic Loci* ; Genetic Predisposition to Disease*; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Oct; Vol. 25 (10), pp. 638-645. Date of Electronic Publication: 2021 Oct Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

PCSK9 E670G (rs505151) Variant and Coronary Artery Disease Risk Among Diabetics.

  • Authors : Mohamed SH; Medical Biochemistry Department, and Faculty of Medicine, University of Zagazig, Zagazig, Egypt.; Hassaan MMM

Subjects: Genetic Predisposition to Disease*; Coronary Artery Disease/Coronary Artery Disease/Coronary Artery Disease/*genetics ; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*complications

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Sep; Vol. 25 (9), pp. 615-623.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Common Variants of the OPG gene Are Associated with Osteoporosis Risk: A Meta-Analysis.

  • Authors : Li X; Department of Orthopedic Trauma, Yuncheng Central Hospital, Shanxi Medical University, Yuncheng, China.; Cheng J

Subjects: Genetic Predisposition to Disease*; Osteoporosis/Osteoporosis/Osteoporosis/*genetics ; Osteoprotegerin/Osteoprotegerin/Osteoprotegerin/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Sep; Vol. 25 (9), pp. 600-610. Date of Electronic Publication: 2021 Sep 09.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association of the MYH6 Gene Polymorphism with the Risk of Atrial Fibrillation and Warfarin Anticoagulation Therapy.

  • Authors : Fu T; Department of Cardiology, Yiwu Central Hospital, Yiwu, China.; Chen M

Subjects: Genetic Predisposition to Disease*; Anticoagulants/Anticoagulants/Anticoagulants/*therapeutic use ; Atrial Fibrillation/Atrial Fibrillation/Atrial Fibrillation/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Sep; Vol. 25 (9), pp. 590-599. Date of Electronic Publication: 2021 Sep 09.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association Between the SLC2A2 Gene rs1499821 Polymorphism and Caries Susceptibility.

  • Authors : Liu L; Guangxi Medical University College of Stomatology, Nanning, China.; Ma F

Subjects: Dental Caries*/Dental Caries*/Dental Caries*/genetics ; Glucose Transporter Type 2*/Glucose Transporter Type 2*/Glucose Transporter Type 2*/genetics; Child

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 May; Vol. 27 (5), pp. 149-156.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Editorial & Opinion

Re: "Association of the Interleukin 1B-31*C Proinflammatory Allele with the Severity of COVID-19 Patients: A Preliminary Report" by Galán-Huerta et al.

Subjects: COVID-19*; Humans ; Alleles

  • Source: Viral immunology [Viral Immunol] 2023 May; Vol. 36 (4), pp. 298. Date of Electronic Publication: 2023 Mar 31.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 Publication Model: Print-Electronic

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  • 10-20 of  979 results for ""Genetic Predisposition to Disease""