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Academic Journal

Allele-Selective LNA Gapmers for the Treatment of Fibrodysplasia Ossificans Progressiva Knock Down the Pathogenic ACVR1 R206H Transcript and Inhibit Osteogenic Differentiation.

  • Authors : Maruyama R; Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.; Nguyen Q

Subjects: Myositis Ossificans*/Myositis Ossificans*/Myositis Ossificans*/genetics ; Myositis Ossificans*/Myositis Ossificans*/Myositis Ossificans*/metabolism ; Myositis Ossificans*/Myositis Ossificans*/Myositis Ossificans*/therapy

  • Source: Nucleic acid therapeutics [Nucleic Acid Ther] 2022 Jun; Vol. 32 (3), pp. 185-193. Date of Electronic Publication: 2022 Jan 27.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101562758 Publication Model: Print-Electronic

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Academic Journal

Impact of Vitamin D Receptor Gene Polymorphism on Systemic Lupus Erythematosus Susceptibility: A Pooled Analysis.

  • Authors : Yang SK; Department of Nephrology and Rheumatology, The Third Xiangya Hospital, Central South University, Changsha, China.; Liu N

Subjects: Lupus Erythematosus, Systemic*/Lupus Erythematosus, Systemic*/Lupus Erythematosus, Systemic*/genetics; Receptors, Calcitriol/Receptors, Calcitriol/Receptors, Calcitriol/*genetics; Alleles

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2022 Apr; Vol. 26 (4), pp. 228-238.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Enhanced Taq Variant Enables Efficient Genome Editing Testing and Mutation Detection.

  • Authors : Du P; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, People's Republic of China.; Li B

Subjects: CRISPR-Cas Systems*/CRISPR-Cas Systems*/CRISPR-Cas Systems*/genetics ; Gene Editing*; Alleles

  • Source: The CRISPR journal [CRISPR J] 2022 Feb; Vol. 5 (1), pp. 131-145. Date of Electronic Publication: 2022 Jan 24.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101738191 Publication Model: Print-Electronic

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Academic Journal

Estimates of West African Ancestry in African Americans Using Alleles of Iron-Related Genes HJV , SLC40A1 , and TFR2 .

  • Authors : Barton JC; Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.; Southern Iron Disorders Center, Birmingham, Alabama, USA.

Subjects: African Americans*/African Americans*/African Americans*/genetics ; Cation Transport Proteins*/Cation Transport Proteins*/Cation Transport Proteins*/genetics ; GPI-Linked Proteins*/GPI-Linked Proteins*/GPI-Linked Proteins*/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2022 Feb; Vol. 26 (2), pp. 96-102.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Lack of Effects of the Genetic Polymorphisms of Interleukin-10 in Clinical Outcomes of COVID-19.

Subjects: Polymorphism, Genetic*; COVID-19/COVID-19/COVID-19/*genetics ; Interleukin-10/Interleukin-10/Interleukin-10/*genetics

  • Source: Viral immunology [Viral Immunol] 2021 Oct; Vol. 34 (8), pp. 567-572. Date of Electronic Publication: 2021 Jun 11.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 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

Identification and Optimization of a Minor Allele-Specific siRNA to Prevent PNPLA3 I148M-Driven Nonalcoholic Fatty Liver Disease.

  • Authors : Murray JK; Therapeutic Discovery, Amgen Research, Thousand Oaks, California, USA.; Long J

Subjects: Non-alcoholic Fatty Liver Disease*/Non-alcoholic Fatty Liver Disease*/Non-alcoholic Fatty Liver Disease*/genetics ; Non-alcoholic Fatty Liver Disease*/Non-alcoholic Fatty Liver Disease*/Non-alcoholic Fatty Liver Disease*/therapy; Alleles

  • Source: Nucleic acid therapeutics [Nucleic Acid Ther] 2021 Oct; Vol. 31 (5), pp. 324-340. Date of Electronic Publication: 2021 Jul 23.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101562758 Publication Model: Print-Electronic

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Academic Journal

Genome Editing Using the CRISPR-Cas9 System to Generate a Solid-Red Germline of Nile Tilapia ( Oreochromis niloticus ).

  • Authors : Segev-Hadar A; Department of Poultry and Aquaculture, Institute of Animal Sciences, Agricultural Research Organization, Volcani Center, Rishon Lezion, Israel; and Institute of Plant Sciences, Agricultural Research Organization, Volcani Center, Rishon Lezion, Israel.

Subjects: Animals, Genetically Modified* ; CRISPR-Cas Systems* ; Gene Editing*

  • Source: The CRISPR journal [CRISPR J] 2021 Aug; Vol. 4 (4), pp. 583-594.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101738191 Publication Model: Print Cited

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Academic Journal

ABCB1 Single Nucleotide Polymorphism Genotypes as Predictors of Paclitaxel-Induced Peripheral Neuropathy in Breast Cancer.

  • Authors : Abdelfattah NM; Clinical Pharmacy Department, Nasser's Institute for Research and Treatment, Cairo, Egypt.; Clinical Pharmacy Department, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.

Subjects: Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics ; Peripheral Nervous System Diseases/Peripheral Nervous System Diseases/Peripheral Nervous System Diseases/*genetics; ATP Binding Cassette Transporter, Subfamily B/ATP Binding Cassette Transporter, Subfamily B/ATP Binding Cassette Transporter, Subfamily B/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jul; Vol. 25 (7), pp. 471-477.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

A Novel Intronic Splicing Mutation in the EXT2 Gene of a Chinese Family with Multiple Osteochondroma.

  • Authors : Guo X; Department of Laboratory Medicine, Fuzhou Second Hospital Affiliated to Xiamen University, Fuzhou, P.R. China.; Chen S

Subjects: Exostoses, Multiple Hereditary/Exostoses, Multiple Hereditary/Exostoses, Multiple Hereditary/*genetics ; N-Acetylglucosaminyltransferases/N-Acetylglucosaminyltransferases/N-Acetylglucosaminyltransferases/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jul; Vol. 25 (7), pp. 478-485.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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