Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Charles J. Macri"'
Publikováno v:
American Journal of Perinatology Reports, Vol 12, Iss 01, Pp e27-e32 (2022)
Objective This survey study aimed to assess patient knowledge, clinical resources, and utilized resources about genetic screening and diagnostic testing. Study Design A one-time anonymous paper survey was distributed to 500 patients at a major urban
Externí odkaz:
https://doaj.org/article/6043df12d06347b3bf2d7d888bffc7e6
Autor:
Xiaohui Tan, Zhongwu Li, Shuchang Ren, Katayoon Rezaei, Qing Pan, Andrew T. Goldstein, Charles J. Macri, Dengfeng Cao, Rachel F. Brem, Sidney W. Fu
Publikováno v:
Breast Cancer Research, Vol 21, Iss 1, Pp 1-14 (2019)
Abstract Background Understanding the molecular alterations associated with breast cancer (BC) progression may lead to more effective strategies for both prevention and management. The current model of BC progression suggests a linear, multistep proc
Externí odkaz:
https://doaj.org/article/e6e2efed2b2e49d5ac78bd4988e682e4
Autor:
Xiaohui Tan, Shuyang Ren, Canyuan Yang, Shuchang Ren, Melinda Z. Fu, Amelia R. Goldstein, Xuelan Li, Leia Mitchell, Jill M. Krapf, Charles J. Macri, Andrew T. Goldstein, Sidney W. Fu
Publikováno v:
Cells, Vol 10, Iss 9, p 2291 (2021)
Lichen sclerosus (LS) is a chronic inflammatory skin disorder with unknown pathogenesis. The aberrant expression of microRNAs (miRNAs) is considered to exert a crucial role in LS. We used the next-generation sequencing technology (RNASeq) for miRNA p
Externí odkaz:
https://doaj.org/article/4a91457f755f444885e3f0c39025ff17
Autor:
Alexis C. Gimovsky, Charles J. Macri
Publikováno v:
Emerging Infectious Diseases, Vol 19, Iss 10, Pp 1693-1694 (2013)
Externí odkaz:
https://doaj.org/article/e56d53367cbd4be6bbb8af91ce68f61f
Autor:
Arianna Prince, Jenna Wade, Alanna Cruz-Bendezú, Charles J. Macri, Nicole Gunawansa, Victoria H. Coleman-Cowger, Jay Schulkin
Publikováno v:
Journal of neonatal-perinatal medicine. 15(4)
Background Genetic screening and testing has only recently become an accessible assessment for genetic risk. Unfortunately, these technologies have been underutilized in minority populations despite their usefulness for predicting diseases like sickl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f251a2cc5192c3afd03256e72339cf46
https://pubmed.ncbi.nlm.nih.gov/35811546
https://pubmed.ncbi.nlm.nih.gov/35811546
Publikováno v:
Journal of Neonatal-Perinatal Medicine. 13:275-278
Background Addison's disease is an uncommon condition encountered during pregnancy; however, pregnant patients with Addison's disease are at higher risk for multiple pregnancy related complications. Treatment during pregnancy involves steroid replace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e4a9454f60894716fa6264e5e31aeb9
https://doi.org/10.3233/npm-190231
https://doi.org/10.3233/npm-190231
Autor:
Andrew T. Goldstein, L. Mitchell, Amelia R Goldstein, Canyuan Yang, Melinda Z. Fu, Xiaohui Tan, Jill M. Krapf, Charles J. Macri, Sidney W. Fu, Shuchang Ren, Shuyang Ren, Xuelan Li
Publikováno v:
Cells
Volume 10
Issue 9
Cells, Vol 10, Iss 2291, p 2291 (2021)
Volume 10
Issue 9
Cells, Vol 10, Iss 2291, p 2291 (2021)
Lichen sclerosus (LS) is a chronic inflammatory skin disorder with unknown pathogenesis. The aberrant expression of microRNAs (miRNAs) is considered to exert a crucial role in LS. We used the next-generation sequencing technology (RNASeq) for miRNA p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04c9e5711bb47913435136ec4fec0c72
Autor:
Alexis C. Gimovsky, Charles J. Macri, Homa K. Ahmadzia, Susanne L. Bathgate, Scott Quinlan, Kathryn Denny
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 34:3750-3755
Despite the increasing trend in delayed childbirth and the known associated complications in advancing maternal age, limited information exists regarding outcomes in very advanced maternal age by delivery type. This study aims to evaluate maternal an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e06bb43124f5411252f21b30d30f24bb
https://doi.org/10.1080/14767058.2019.1691989
https://doi.org/10.1080/14767058.2019.1691989
Publikováno v:
Journal of Neonatal-Perinatal Medicine. :1-6
We report a case of two consecutive pregnancies in the same couple presenting with very low pregnancy-associated plasma protein A (PAPP-A), with both pregnancies affected by multiple anomalies of a similar phenotype identified during mid-trimester ul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3784be6f953165f53aedf5be1fbb3a5a
https://doi.org/10.3233/npm-181854
https://doi.org/10.3233/npm-181854
Publikováno v:
American Journal of Perinatology Reports, Vol 12, Iss 01, Pp e27-e32 (2022)
Objective This survey study aimed to assess patient knowledge, clinical resources, and utilized resources about genetic screening and diagnostic testing. Study Design A one-time anonymous paper survey was distributed to 500 patients at a major urban
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d48ff57f3e8b79e8e7e6e546ec7304da
https://pubmed.ncbi.nlm.nih.gov/35141032
https://pubmed.ncbi.nlm.nih.gov/35141032