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Academic Journal

ApoE Modifier Alleles for Alzheimer's Disease Discovered by Information Theory Dependency Measures: MIST Software Package.

Subjects: Alzheimer Disease*/Alzheimer Disease*/Alzheimer Disease*/genetics; Humans ; Alleles

  • Source: Journal of computational biology : a journal of computational molecular cell biology [J Comput Biol] 2023 Mar; Vol. 30 (3), pp. 323-336. Date of Electronic Publication: 2022 Nov Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9433358 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: Black or African American*/Black or African American*/Black or African American*/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

Analyses of the Genetic Polymorphisms rs3740199 and rs1871054 of the ADAM12 Gene and the Alleles at the rs2073508 Loci of the TGFB1 Gene and Their Contribution to Susceptibility to Primary Knee Osteoarthritis.

Subjects: ADAM12 Protein/ADAM12 Protein/ADAM12 Protein/*genetics ; Osteoarthritis, Knee/Osteoarthritis, Knee/Osteoarthritis, Knee/*genetics ; Transforming Growth Factor beta1/Transforming Growth Factor beta1/Transforming Growth Factor beta1/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Jun; Vol. 24 (6), pp. 375-380. Date of Electronic Publication: 2020 Apr 06.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

A Tandem Guide RNA-Based Strategy for Efficient CRISPR Gene Editing of Cell Populations with Low Heterogeneity of Edited Alleles.

Subjects: CRISPR-Cas Systems/CRISPR-Cas Systems/CRISPR-Cas Systems/*genetics ; Gene Editing/Gene Editing/Gene Editing/*methods ; Gene Knockout Techniques/Gene Knockout Techniques/Gene Knockout Techniques/*methods

  • Source: The CRISPR journal [CRISPR J] 2020 Apr; Vol. 3 (2), pp. 123-134.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101738191 Publication Model: Print Cited

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Academic Journal

Association of HLA-A, -B, DRB, and DQB Alleles with Persistent HPV-16 Infection in Women from Tamil Nadu, India.

  • Authors : Bhaskaran M; Human Genomics Laboratory, Centre for Research in Infectious Disease (CRID), School of Chemical and Biotechnology, SASTRA Deemed University, Thanjavur, India.; Murali SV

Subjects: HLA-D Antigens/HLA-D Antigens/HLA-D Antigens/*genetics ; Histocompatibility Antigens Class I/Histocompatibility Antigens Class I/Histocompatibility Antigens Class I/*genetics ; Human papillomavirus 16/Human papillomavirus 16/Human papillomavirus 16/*immunology

  • Source: Viral immunology [Viral Immunol] 2019 Dec; Vol. 32 (10), pp. 430-441. Date of Electronic Publication: 2019 Dec 03.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 Publication Model: Print-Electronic

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Academic Journal

HLA-A, -B, -DRB1 Alleles as Genetic Predictive Factors for Dengue Disease: A Systematic Review and Meta-Analysis.

  • Authors : Chen Y; 1 Department of Clinical Laboratory Medicine, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.; Liao Y

Subjects: Genetic Predisposition to Disease*; Dengue/Dengue/Dengue/*genetics ; HLA-A Antigens/HLA-A Antigens/HLA-A Antigens/*genetics

  • Source: Viral immunology [Viral Immunol] 2019 Apr; Vol. 32 (3), pp. 121-130. Date of Electronic Publication: 2019 Mar 05.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 Publication Model: Print-Electronic

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Academic Journal

Crohn's Disease Candidate Gene Alleles Predict Time to Progression from Inflammatory B1 to Stricturing B2, or Penetrating B3 Phenotype.

  • Authors : Pernat Drobež C; 1 Department of Gastroenterology, University Medical Centre Maribor , Maribor, Slovenia .; Ferkolj I

Subjects: Gene Frequency* ; Genetic Markers* ; Genetic Predisposition to Disease*

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2018 Mar; Vol. 22 (3), pp. 143-151. Date of Electronic Publication: 2018 Feb 15.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Linkage of Metabolic Defects to Activated PIK3CA Alleles in Endothelial Cells Derived from Lymphatic Malformation.

  • Authors : Glaser K; 1 Department of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital and Medical Center , Cincinnati, Ohio.; Dickie P

Subjects: Alleles*; Class I Phosphatidylinositol 3-Kinases/Class I Phosphatidylinositol 3-Kinases/Class I Phosphatidylinositol 3-Kinases/*genetics ; Endothelial Cells/Endothelial Cells/Endothelial Cells/*metabolism

  • Source: Lymphatic research and biology [Lymphat Res Biol] 2018 Feb; Vol. 16 (1), pp. 43-55. Date of Electronic Publication: 2018 Jan 18.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101163587 Publication Model: Print-Electronic

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Academic Journal

A streamlined CRISPR pipeline to reliably generate zebrafish frameshifting alleles.

  • Authors : Talbot JC; 1 Department of Molecular Genetics, The Ohio State University , Columbus, Ohio.; Amacher SL

Subjects: Alleles*; CRISPR-Cas Systems/CRISPR-Cas Systems/CRISPR-Cas Systems/*genetics ; Frameshift Mutation/Frameshift Mutation/Frameshift Mutation/*genetics

  • Source: Zebrafish [Zebrafish] 2014 Dec; Vol. 11 (6), pp. 583-5.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101225070 Publication Model: Print Cited

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Academic Journal

New and rare GJB2 alleles in patients with nonsyndromic sensorineural hearing impairment: a genotype/auditory phenotype correlation.

  • Authors : Stanghellini I; 1 Medical Genetics Unit, Department of Mother & Child, University Hospital of Modena , Modena, Italy .; Genovese E

Subjects: Alleles* ; Gene Frequency* ; Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/Hearing Loss, Sensorineural*/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2014 Dec; Vol. 18 (12), pp. 839-44.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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