Technology
Applications
Resources
Support
Company
Contact
EN
EN
- Global
CN
- 中国
menu
Close
Home
Technology
Applications
Pharmacogenetics
Liquid Biopsy
Mutation Profiling
Hereditary Genetics
Methylation
Sample Integrity
Specimen Validity
Services
Assays by Agena
Certified Service Providers
Resources
Recent Articles
Publication Library
Product Literature
Support
Service Plans
Distributors
Certified Service Providers
Company
Careers
Press
Contact
Customer Support Portal
Home
Technology
Applications
Pharmacogenetics
Mutation Profiling
Liquid Biopsy
Hereditary Genetics
Methylation
Sample Integrity
Specimen Validity
Services
Assays by Agena
Certified Service Providers
Resources
Blog Articles
Publication Library
Product Literature
Support
Service Plans
Distributors
Certified Service Providers
Company
Careers
Press
Contact
Customer Support Portal
Phone: (858) 882-2800
Home
/
Resources
/
Publication Library
Search Results for: Hereditary Genetics
Search All publications
How recent?
Search
Interferon lambda polymorphisms associate with body iron indices and hepatic expression of interferon-responsive long non-coding RNA in chronic hepatitis …
Association of genetic polymorphisms in MIF with breast cancer risk in Chinese women
Implication of the rs670 variant of APOA1 gene with lipid profile, serum adipokine levels and components of metabolic syndrome in adult obese subjects
Prognostic value of the VHL, HIF-1α, and VEGF signaling pathway and associated MAPK (ERK1/2 and ERK5) pathways in clear-cell renal cell carcinoma. a long-term …
Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease‐causing variants
CCR6, IL7R, FAS and Madcam-1 Single Nucleotide Polymorphisms Are Associated with Higher Incidence of Infections in Allogeneic Stem-Cell Transplant from a …
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1,-2 and-3 and Is Associated with Risk for Multiple Sclerosis
Genetic Variations of CYP19A1 Gene and Stroke Susceptibility: A Case-control Study in the Chinese Han Population
A functional variant in CHK1 contributes to increased risk of nasopharyngeal carcinoma in a Han Chinese population
Structural and functional alterations of Nitric Oxide Synthase 3 due to missense variants associate with High-Altitude Pulmonary Edema through Dynamic study
«
...
10
20
30
...
198
199
200
201
202
...
210
220
230
...
»