Zobrazeno 1 - 10
of 383
pro vyhledávání: '"Henry A. Erlich"'
Autor:
Eleonora Loi, Loredana Moi, Paola Cabras, Giulia Arduino, Giulia Costanzo, Stefano Del Giacco, Henry A. Erlich, Davide Firinu, Aldo Caddori, Patrizia Zavattari
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
One of the mechanisms by which viruses can evade the host’s immune system is to modify the host’s DNA methylation pattern. This work aims to investigate the DNA methylation and gene expression profile of COVID-19 patients, divided into symptomati
Externí odkaz:
https://doaj.org/article/fae70aba569c44ad81d9dab281b326a1
Autor:
Philip E. Castle, Robert D. Burk, Brian Befano, Thanh Tam, Henry A. Erlich, Carrie Aldrich, Raymond Apple, Janet R. Kornegay, Nicolas Wentzensen, Julia C. Gage, Hormuzd A. Katki, Tina Raine-Bennett, Sean Boyle, Mark Schiffman
Background: The cobas HPV Test (“cobas”; Roche Molecular Systems) detects HPV16 and HPV18 individually, and a pool of 12 other high-risk (HR) HPV types. The test is approved for (i) atypical squamous cells of undetermined significance (ASC-US) tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd8b572fbe0c6e6c727e7f61194ab5e
https://doi.org/10.1158/1055-9965.c.6516045
https://doi.org/10.1158/1055-9965.c.6516045
Autor:
Ashutosh Lal, Christian López-Peña, Gunmeet Bali, Cassandra D Calloway, Hugh Salamon, Katie T. Carlberg, Henry A. Erlich, Shelly Shih, Ken D. Yamaguchi, Reena Das
Publikováno v:
The Journal of Applied Laboratory Medicine. 7:515-531
Background Noninvasive prenatal testing (NIPT) of chromosomal aneuploidies based on next-generation sequencing (NGS) analysis of fetal DNA in maternal plasma is well established, but testing for autosomal recessive disorders remains challenging. NGS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e549f36b7a98769a8348c9174737f88f
https://doi.org/10.1093/jalm/jfab118
https://doi.org/10.1093/jalm/jfab118
Publikováno v:
Forensic Science International: Genetics Supplement Series. 7:658-660
To analyze crime scene evidence with degraded DNA, we have designed a probe capture Next Generation Sequencing system for targeted enrichment for both nuclear SNP markers and for the entire mitochondrial DNA genome. This probe capture NGS system was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7172d60a067e7827122faaad30938db0
https://doi.org/10.1016/j.fsigss.2019.10.128
https://doi.org/10.1016/j.fsigss.2019.10.128
Autor:
Alessandra La Vaccara, Fredy A. Peccerelli, Ranit Mishori, Eric Stover, Sara H. Katsanis, Henry A. Erlich, Curren W. Warf, Patricia Vásquez, Daniel R. Berger, Elizabeth S. Barnert, M. Veronica Svetaz, Diana Madden, Mariana Herrera Piñero, Jennifer K. Wagner, Michael Stebbins, Andreas Kleiser, Thomas J. Parsons, Thomas J. White, Kathryn Hampton, Richard F. Selden
Publikováno v:
Science
Perceived lack of tools, and fears of the sensitivity of DNA data, should not be obstacles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b227e0eabe6e0b9446c6abe106d67edc
https://europepmc.org/articles/PMC9185756/
https://europepmc.org/articles/PMC9185756/
Autor:
Henry A. Erlich
The same DNA technology that allows the analysis of a hair or tiny blood spot at a crime scene also enables sequencing the DNA of a bone fragment from a Neanderthal skeleton. Comparing the DNA sequences of different samples and comparing the frequenc
Publikováno v:
Forensic science international. Genetics. 53
Interpreting mixtures with nuclear genetic markers remains one of the persisting challenges in forensic DNA analysis, particularly when the DNA is degraded or present in trace amounts. In these scenarios, analyzing mitochondrial (mt) DNA can be usefu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92f59c94bc6e198c9ff76d7500ae82fd
https://pubmed.ncbi.nlm.nih.gov/34052577
https://pubmed.ncbi.nlm.nih.gov/34052577
Publikováno v:
Silent Witness
The current standard of forensic DNA analysis is genotyping the length polymorphism of STR loci by capillary electrophoresis and analyzing the polymorphism of mitochondrial DNA by Sanger sequencing. However, the trend of dramatic technological develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58ac5ad76c7a3f1c7fca6006f1b510dd
https://doi.org/10.1093/oso/9780190909444.003.0006
https://doi.org/10.1093/oso/9780190909444.003.0006
Autor:
Henry A. Erlich, Kazutoyo Osoegawa, David A. Noonan, Elizabeth Trachtenberg, Julia Udell, Franziska Cohen, Jorge R. Oksenberg, Steven J. Mack, Martha Ladner, Sharon K. Hawbecker, Damian Goodridge
Publikováno v:
Genes and immunity, vol 20, iss 4
We investigated association between HLA class I and class II alleles and haplotypes, and KIR loci and their HLA class I ligands, with multiple sclerosis (MS) in 412 European American MS patients and 419 ethnically matched controls, using next-generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adc984606e6af4cfc3fbca871a08662e
https://escholarship.org/uc/item/9mj0j3bk
https://escholarship.org/uc/item/9mj0j3bk
Autor:
Wei-Min Chen, Henry A. Erlich, Patrick Concannon, Emily Farber, Search for Diabetes in Youth, Ronny A. Bell, Zhennan Zhu, Lynne E. Wagenknecht, Mark A. Atkinson, Jeffrey C. Edberg, Stephen S. Rich, Steven R. Brant, Mary Helen Black, Andrea K. Steck, Jorge R. Oksenberg, Jasmin Divers, S. Louis Bridges, Catherine Pihoker, Peter K. Gregersen, Robert P. Kimberly, Marian Rewers, Suna Onengut-Gumuscu, Dana Dabelea, Jessica K. Bonnie, Catherine C. Robertson
OBJECTIVE Genetic risk scores (GRS) have been developed that differentiate individuals with type 1 diabetes from those with other forms of diabetes and are starting to be used for population screening; however, most studies were conducted in European
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9576b43c92f122bde993559f4bc0e528
https://europepmc.org/articles/PMC6385701/
https://europepmc.org/articles/PMC6385701/