Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Gary L. Harton"'
Autor:
Zandra C. Deans, Anil Biricik, Martine De Rycke, Gary L. Harton, Miroslav Hornak, Farrah Khawaja, Céline Moutou, Jan Traeger‐Synodinos, Pamela Renwick
Objective: Genomics Quality Assessment has provided external quality assessments (EQAs) for preimplantation genetic testing (PGT) for 12 years for eight monogenic diseases to identify sub-optimal PGT strategies, testing and reporting of results, whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::417eb81f65a16dda1afb286616a4b3a4
https://biblio.vub.ac.be/vubir/twelve-years-of-assessing-the-quality-of-preimplantation-genetic-testing-for-monogenic-disorders(70c133c4-a853-4ad5-8dd4-0dfb9a0ed4cd).html
https://biblio.vub.ac.be/vubir/twelve-years-of-assessing-the-quality-of-preimplantation-genetic-testing-for-monogenic-disorders(70c133c4-a853-4ad5-8dd4-0dfb9a0ed4cd).html
Autor:
Jon S. Zawistowski, Isai Salas-Gonzalez, Tia A. Tate, Tatiana V. Morozova, Katherine Kennedy, Durga M. Arvapalli, Swetha D. Velivela, Jamie E. Remington, Josh Croteau, Kevin Taylor, Jeff G. Blackinton, Victor J. Weigman, Jeffrey R. Marks, Eun-Sil Shelley Hwang, Gary L. Harton, Jay A. West
Publikováno v:
Cancer Research. 83:5933-5933
The ResolveOME™ single-cell amplification solution unites whole-genome and full-length transcriptome information from the same cell, providing critical insight between these layers not possible when analyzed in isolation. We expand here upon the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acb7d91a61bb75597bd216b55b3a9149
https://doi.org/10.1158/1538-7445.am2023-5933
https://doi.org/10.1158/1538-7445.am2023-5933
Autor:
Jon S. Zawistowski, Isai Salas-González, Tatiana V. Morozova, Jeff G. Blackinton, Tia Tate, Durga Arvapalli, Swetha Velivela, Gary L. Harton, Jeffrey R. Marks, E. Shelley Hwang, Victor J. Weigman, Jay A.A. West
Discovering genomic variation in the absence of information about transcriptional consequence of that variation or, conversely, a transcriptional signature without understanding underlying genomic contributions, hinders understanding of molecular mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f02b57120e0460e9c1b8272715c52b35
https://doi.org/10.1101/2022.04.29.489440
https://doi.org/10.1101/2022.04.29.489440
Autor:
Thu Hien Le Thi, Nga Pham Thuy, Vinh Nguyen Quang, Gary L Harton, Nhung Hoang Thi, Huynh Nguyen Van, Duc Nguyen Minh, Anh Dao Mai, Quan Tran Quoc
Publikováno v:
Journal of Assisted Reproduction and Genetics
Purpose The purpose of this research is to study the clinical outcomes using a next-generation sequencing-based protocol allowing for simultaneous testing of mutations in the beta thalassemia (HBB) gene, including single nucleotide polymorphism (SNP)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f246ef7482ace84e4aa8beb034a3f421
http://europepmc.org/articles/PMC7884556
http://europepmc.org/articles/PMC7884556
PHÁT TRIỂN VÀ ÁP DỤNG XÉT NGHIỆM DI TRUYỀN TRƯỚC CHUYỂN PHÔI (PGT-M) CHO BỆNH THALASSEMIA Ở VIỆT NAM
Autor:
Gary L Harton, Đào Mai Anh, Hoàng Thị Nhung, Nguyễn Quang Vinh, Nguyễn Minh Đức, Lê Thị Thu Hiền, Nguyễn Văn Huynh, Trần Quốc Quân, Phạm Thúy Nga
Publikováno v:
Tạp chí Y học Việt Nam. 500
Mục tiêu: Thiết kế, tối ưu và xây dựng quy trình cho thực hiện đồng thời xét nghiệm PGT-A và PGT-M cho bệnh thalassemia, sử dụng hệ thống giải trình tự thế hệ mới cho phép kiểm tra đồng thời c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a3b7ce53e41e739cd74372e80b335e6
https://doi.org/10.51298/vmj.v500i2.364
https://doi.org/10.51298/vmj.v500i2.364
Autor:
Darren K. Griffin, Gary L. Harton
Preimplantation genetic testing (PGT) is now well established as a valuable treatment option for patients wishing to start or continue a family, for a range of indications from advanced maternal age to high risk of transmitting inherited disease. Thi
Autor:
Karen Sage, Gary L. Harton, Christian S. Ottolini, Alan H. Handyside, Senthil A Natesan, Darren K. Griffin, Nabeel A. Affara, Alan R. Thornhill, Dagan Wells, Kerry M. Cliffe, Jon Taylor, M. Konstantinidis
Publikováno v:
Journal of Assisted Reproduction and Genetics
Preimplantation genetic diagnosis (PGD) of single gene defects by genetic analysis of single or small numbers of cells biopsied from in vitro fertilization (IVF) embryos is clinically well-established. Targeted haplotyping by multiplex fluorescent po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::487c889694f6ffb20fe1c016cf293e74
https://doi.org/10.1007/s10815-014-0405-y
https://doi.org/10.1007/s10815-014-0405-y
Autor:
Helen G. Tempest, Gary L Harton
Publikováno v:
Asian Journal of Andrology. 14:32-39
Infertility in humans is surprisingly common occurring in approximately 15% of the population wishing to start a family. Despite this, the molecular and genetic factors underlying the cause of infertility remain largely undiscovered. Nevertheless, mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416c812e736c394e5c9bc24db7e318b1
https://doi.org/10.1038/aja.2011.66
https://doi.org/10.1038/aja.2011.66
Autor:
Gary L. Harton, Dagan Wells
Publikováno v:
Screening the Single Euploid Embryo ISBN: 9783319168913
Aneuploidy is a broad term used to describe gross chromosomal imbalance in an organism. For the sake of this chapter, only aneuploidy in an embryo will be considered. Aneuploidy typically presents as either an additional chromosome (e.g., trisomy) or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::532026a1ccb3d7ea13936a0f60fb6cfb
https://doi.org/10.1007/978-3-319-16892-0_13
https://doi.org/10.1007/978-3-319-16892-0_13
Autor:
Stanley M. Berry, Jan M. Lanouette, Paul Van Ballaer, C. Sohn, E.M. Anderson, Eric L. Krivchenia, Amitabha Mazumder, M. Schiesser, Charles H. Rodeck, D.T.Y. Liu, Veerie A.C. Evrard, Takefumi Bessho, Jan Deprest, Ai Guo Wu, John E. Gardener, Mark P. Johnson, Donald S. Emerson, Owen P. Phillips, Ivo Brosens, Jocelyn Brookes, Jeffrey S. Dungan, G. Bastert, Debra Duquette, Kazuko Sakata, R. Kurek, D.R.E. Jones, Maria Michejda, Gary L. Harton, Joseph D. Schulman, Hideaki Sawai, Toni Lerut, Karen H. Hagglund, Michael W. Kilpatrick, Udit Verma, Kamiel Vandenberghe, Faisal Qureshi, Joseph A. Bellanti, U. Hahn, Leonidas A. Phylactou, Gene Levinson, Hiroyuki Tanaka, Lee P. Shulman, Jing Deng, Susan H. Black, William R. Lees, D. Wallwiener, Edward F. Fugger, Koji Koyama, Shinji Komori, Susan J. Sherman, Faris K. Ahmad, A.A. Evans, Petros Tsipouras, Suzanne M. Jacques
Publikováno v:
Fetal Diagnosis and Therapy. 11:I-V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2141143b62b861b9aac2cd424c747b0
https://doi.org/10.1159/000264349
https://doi.org/10.1159/000264349