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A multivariable prediction model for intra-amniotic infection in patients with preterm labor and intact membranes including a point of care system that measures amniotic fluid MMP-8.
Cobo T, Ferrero S, Haavisto A, Luokola P, Sanchez-Garcia AB, Bosch J, Gené A, Murillo C, Rueda C, González-de la Presa B, Santamaria S, Ponce J, Boada D, Palacio M. Cobo T, et al. Among authors: gene a. J Perinat Med. 2023 Dec 15;52(2):136-142. doi: 10.1515/jpm-2023-0405. Print 2024 Feb 26. J Perinat Med. 2023. PMID: 38098237 Free article.
METHODS: From 2019 to 2022, we prospectively included pregnant patients admitted below 34.0 weeks with diagnosis of PTL and had undergone amniocentesis to rule in/out IAI. The main outcome was IAI, defined by a positive culture and/or 16S ribosomal RNA gene in amnio …
METHODS: From 2019 to 2022, we prospectively included pregnant patients admitted below 34.0 weeks with diagnosis of PTL and had undergone am …
Differences in Drug-Susceptibility Patterns between Mycobacterium avium, Mycobacterium intracellulare, and Mycobacterium chimaera Clinical Isolates: Prospective 8.5-Year Analysis by Three Laboratories.
Fernandez-Pittol M, Batista-Arnau S, Román A, San Nicolás L, Oliver L, González-Moreno O, Martínez JA, Amaro-Rodríguez R, Soler N, Gené A, González-Cuevas A, Tudó G, Gonzalez-Martin J. Fernandez-Pittol M, et al. Among authors: gene a. Antibiotics (Basel). 2022 Dec 29;12(1):64. doi: 10.3390/antibiotics12010064. Antibiotics (Basel). 2022. PMID: 36671265 Free PMC article.
DIAPH2 gene polymorphisms and laryngeal cancer risk in men.
Cichocka E, Górczyńska-Kosiorz S, Misiołek M, Ścierski W, Koniewska A, Stryjewska-Makuch G, Gumprecht J. Cichocka E, et al. J Cancer Res Clin Oncol. 2024 Jun 7;150(6):295. doi: 10.1007/s00432-024-05820-4. J Cancer Res Clin Oncol. 2024. PMID: 38844723
BACKGROUND: The DIAPH2 gene is one of the genes commonly associated with laryngeal squamous cell carcinoma (LSCC). ...RESULTS: In the case of the rs12851931 polymorphism in the DIAPH2 gene, a significant difference was observed in the distribution of the T st …
BACKGROUND: The DIAPH2 gene is one of the genes commonly associated with laryngeal squamous cell carcinoma (LSCC). ...RESULTS: In the …
Structural and genetic basis for the binding of a mouse monoclonal antibody to Flavobacterium psychrophilum lipopolysaccharide.
Cisar JO, Wang X, Woods RJ, Cain KD, Wiens GD. Cisar JO, et al. J Fish Dis. 2024 Jun 4:e13958. doi: 10.1111/jfd.13958. Online ahead of print. J Fish Dis. 2024. PMID: 38837770
Additionally, mAb binding was approximately 5-times stronger to homologous Fp CSF259-93 LPS than to LPS from a strain with a different R-group gene. A conformational epitope for mAb FL100A binding was suggested from molecular dynamic simulations of each O-PS. ...
Additionally, mAb binding was approximately 5-times stronger to homologous Fp CSF259-93 LPS than to LPS from a strain with a different R-gro …
Impact of genome build on RNA-seq interpretation and diagnostics.
Ungar RA, Goddard PC, Jensen TD, Degalez F, Smith KS, Jin CA; Undiagnosed Diseases Network; Bonner DE, Bernstein JA, Wheeler MT, Montgomery SB. Ungar RA, et al. Am J Hum Genet. 2024 May 31:S0002-9297(24)00168-X. doi: 10.1016/j.ajhg.2024.05.005. Online ahead of print. Am J Hum Genet. 2024. PMID: 38834072
Across six routinely collected biospecimens, 61% of quantified genes were not influenced by genome build. However, we identified 1,492 genes with build-dependent quantification, 3,377 genes with build-exclusive expression, and 9,077 genes with annotati …
Across six routinely collected biospecimens, 61% of quantified genes were not influenced by genome build. However, we identified 1,49 …
Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings.
Rizkallah D, Daher RT, Haddad L, Karam PE. Rizkallah D, et al. Metab Brain Dis. 2024 Jun 4. doi: 10.1007/s11011-024-01366-z. Online ahead of print. Metab Brain Dis. 2024. PMID: 38833093
Whole exome sequencing revealed a homozygous variant, p.Phe188del, in the SLC25A15 gene, a French- Canadian founder mutation previously unreported in Arab patients. ...
Whole exome sequencing revealed a homozygous variant, p.Phe188del, in the SLC25A15 gene, a French- Canadian founder mutation p …
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