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Editorial & Opinion

A Novel Genetic Candidate for Primary Lymphedema.

  • Authors : Rockson SG; Stanford University School of Medicine, Stanford, California, USA.

Subjects: Genetic Predisposition to Disease* ; Lymphedema*/Lymphedema*/Lymphedema*/diagnosis ; Lymphedema*/Lymphedema*/Lymphedema*/genetics

  • Source: Lymphatic research and biology [Lymphat Res Biol] 2022 Oct; Vol. 20 (5), pp. 467.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101163587 Publication Model: Print Cited

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Academic Journal

The Association Between the PTPN22 C1858T Variant and Vasculitis: A Meta-analysis Update with Trial Sequential Analysis.

  • Authors : Lee YH; Division of Rheumatology, Korea University Anam Hospital, Seoul, Korea.; Song GG

Subjects: Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/genetics ; Vasculitis*/Vasculitis*/Vasculitis*/genetics; Humans

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2022 Oct; Vol. 26 (10), pp. 492-500.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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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

Correlation Between Polymorphisms of the SIRT1 Gene microRNA Target Sites and Diabetic Nephropathy.

  • Authors : Sun Y; Department of Endocrinology and Metabolism, Zhuji People's Hospital of Zhejiang Province, Zhuji, China.; Wang J

Subjects: Genetic Predisposition to Disease*; Diabetic Nephropathies/Diabetic Nephropathies/Diabetic Nephropathies/*genetics ; Sirtuin 1/Sirtuin 1/Sirtuin 1/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jun; Vol. 25 (6), pp. 387-398.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Influence of Lysyl oxidase Polymorphisms in Cancer Risk: An Updated Meta-analysis.

Subjects: Genetic Predisposition to Disease*; Biomarkers, Tumor/Biomarkers, Tumor/Biomarkers, Tumor/*genetics ; Carcinogenesis/Carcinogenesis/Carcinogenesis/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jun; Vol. 25 (6), pp. 411-418. Date of Electronic Publication: 2021 May 27.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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  • 1-10 of  979 results for ""Genetic Predisposition to Disease""