Zobrazeno 1 - 10
of 967
pro vyhledávání: '"A R, Berman"'
Publikováno v:
Maternal Health, Neonatology and Perinatology, Vol 10, Iss 1, Pp 1-7 (2024)
Abstract Background To characterize the demographics of a modern hospitalized antepartum population, compare the morbidities of this subset to national morbidity trends, and identify predictors of satisfaction during hospitalization to inform opportu
Externí odkaz:
https://doaj.org/article/f4ca07dfecf64e69baff6b55327eb05e
Autor:
Hans M Dalton, Naomi J Young, Alexys R Berman, Heather D Evans, Sydney J Peterson, Kaylee A Patterson, Clement Y Chow
Publikováno v:
PLoS Genetics, Vol 20, Iss 10, p e1011458 (2024)
DPAGT1-CDG is a Congenital Disorder of Glycosylation (CDG) that lacks effective therapies. It is caused by mutations in the gene DPAGT1 which encodes the first enzyme in N-linked glycosylation. We used a Drosophila rough eye model of DPAGT1-CDG with
Externí odkaz:
https://doaj.org/article/ab31bd68f505493d9707b2f91705c247
Autor:
Alyssa R. Berman, Andrew J. Specht, Rebeca A. Castro, Kirsten L. Cooke, Shir Gilor, Autumn N. Harris
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 38, Iss 2, Pp 1068-1073 (2024)
Abstract Background Ammonium excretion decreases as kidney function decreases in several species, including cats, and may have predictive or prognostic value in patients with chronic kidney disease (CKD). Urine ammonia measurement is not readily avai
Externí odkaz:
https://doaj.org/article/6de969091eff4f17858bff514e387076
Autor:
Juliet Aizer, Erika L. Abramson, Jessica R. Berman, Stephen A. Paget, Marianna B. Frey, Victoria Cooley, Ying Li, Katherine L. Hoffman, Julie A. Schell, Michael D. Tiongson, Myriam A. Lin, Lisa A. Mandl
Publikováno v:
ACR Open Rheumatology, Vol 5, Iss 1, Pp 4-9 (2023)
Objective Self‐efficacy, the internal belief that one can perform a specific task successfully, influences behavior. To promote critical appraisal of medical literature, rheumatology training programs should foster both competence and self‐effica
Externí odkaz:
https://doaj.org/article/45c731111b264b8eab329ecb1bf2778f
Autor:
Ningyi Zhang, Sarah R. Berman, Dominique Joubert, Silvere Vialet-Chabrand, Leo F. M. Marcelis, Elias Kaiser
Publikováno v:
Frontiers in Plant Science, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/c8e5900751b14b60bbc88e389a2178d2
Autor:
Gregory E Alexander, Wendy Lin, Fabian E Ortega, Madhuvanthi Ramaiah, Byoungsok Jung, Lijuan Ji, Ekaterina Revenkova, Payal Shah, Christian Croisetiere, Jennifer R Berman, Lane Eubank, Gunjan Naik, Jacqueline Brooks, Andrea Mich, Seyedmehdi Shojaee, Neda Ronaghi, Hemanshi Chawla, Xinyi Hou, Qinwen Liu, Christopher-James A V Yakym, Patriss Wais Moradi, Meredith Halks-Miller, Alexander M Aravanis, Sonya Parpart-Li, Nathan Hunkapiller
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0283001 (2023)
The analytical validation is reported for a targeted methylation-based cell-free DNA multi-cancer early detection test designed to detect cancer and predict the cancer signal origin (tissue of origin). A machine-learning classifier was used to analyz
Externí odkaz:
https://doaj.org/article/dd8363d94bd1437795386bee9e3165cc
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0275047 (2023)
The conversion of supplemental greenhouse light energy into biomass is not always optimal. Recent trends in global energy prices and discussions on climate change highlight the need to reduce our energy footprint associated with the use of supplement
Externí odkaz:
https://doaj.org/article/071b0cb2fe04489087b0f212a8c02a65
Autor:
R. Berman, W. Dampier, A. Atkins, A. Allen, V. Pirrone, S. Passic, A. Ahmed, Z. Szep, M. Nonnemacher, B. Wigdahl
Publikováno v:
Journal of Virus Eradication, Vol 8, Iss , Pp 100258- (2022)
Externí odkaz:
https://doaj.org/article/33eada2b12eb4af7b61072e0469a9464
Autor:
Hans M Dalton, Raghuvir Viswanatha, Roderick Brathwaite, Jae Sophia Zuno, Alexys R Berman, Rebekah Rushforth, Stephanie E Mohr, Norbert Perrimon, Clement Y Chow
Publikováno v:
PLoS Genetics, Vol 18, Iss 9, p e1010430 (2022)
Partial loss-of-function mutations in glycosylation pathways underlie a set of rare diseases called Congenital Disorders of Glycosylation (CDGs). In particular, DPAGT1-CDG is caused by mutations in the gene encoding the first step in N-glycosylation,
Externí odkaz:
https://doaj.org/article/bbc74efb857641bd92e0108b5c183c6e
Publikováno v:
PLoS Genetics, Vol 18, Iss 6 (2022)
NGLY1 deficiency, a rare disease with no effective treatment, is caused by autosomal recessive, loss-of-function mutations in the N-glycanase 1 (NGLY1) gene and is characterized by global developmental delay, hypotonia, alacrima, and seizures. We use
Externí odkaz:
https://doaj.org/article/a3ea1336b01f4a54b35171cbefbf3fc4