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Showing 457 to 461 of 461 entries
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Nutrient supply, cell spatial correlation and Gompertzian tumor growth.

Theory in biosciences = Theorie in den Biowissenschaften

Castorina P, Carco' D.
PMID: 33988848
Theory Biosci. 2021 Jun;140(2):197-203. doi: 10.1007/s12064-021-00344-8. Epub 2021 May 14.

Gompertzian tumor growth can be reproduced by mitosis, related to nutrient supply, with local spatial cell correlations. The global energy constraint alone does not reproduce in vivo data by the observed values of the nutrient expenditure for the cell...

Complete genome sequence of the biocontrol yeast Papiliotrema terrestris strain LS28.

G3 (Bethesda, Md.)

Palmieri D, Barone G, Cigliano RA, De Curtis F, Lima G, Castoria R, Ianiri G.
PMID: 34534326
G3 (Bethesda). 2021 Dec 08;11(12). doi: 10.1093/g3journal/jkab332.

Papiliotrema terrestris strain LS28 is a biocontrol agent selected for its antagonistic activity against several plant pathogens both in the field and postharvest. The availability of a genome sequencing sets the foundation for the identification of the genetic mechanisms...

Chemoradiotherapy followed by Active Surveillance Versus Standard Esophagectomy for Esophageal Cancer: A Systematic Review and Individual Patient Data Meta-Analysis.

Annals of surgery

van der Wilk BJ, Eyck BM, Hofstetter WL, Ajani JA, Piessen G, Castoro C, Alfieri R, Kim JH, Kim SB, Furlong H, Walsh TN, Nieboer D, Wijnhoven BPL, Lagarde SM, Lanschot JJBV.
PMID: 34191461
Ann Surg. 2021 May 11; doi: 10.1097/SLA.0000000000004930. Epub 2021 May 11.

OBJECTIVE: To compare overall survival of patients with a clinically complete response (cCR) undergoing active surveillance versus standard esophagectomy.SUMMARY BACKGROUND DATA: One-third of patients with esophageal cancer have a pathologically complete response in the resection specimen after neoadjuvant chemoradiotherapy....

Craniosynostosis is a feature of CHD7-related CHARGE syndrome.

American journal of medical genetics. Part A

De Luca C, Picone S, Cassina M, Marziali S, Morlino S, Camerota L, Tamburrini G, Castori M, Paolillo P, Salviati L, Brancati F.
PMID: 33844462
Am J Med Genet A. 2021 Jul;185(7):2160-2163. doi: 10.1002/ajmg.a.62208. Epub 2021 Apr 12.

CHARGE syndrome is a rare genetic multiple-malformation disorder characterized by wide phenotypic variability. It is often caused by heterozygous variants in CHD7 and, more rarely, SEMA3E. Although craniofacial alterations are frequent in this condition, to date craniosynostosis is not...

X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases.

Frontiers in medicine

Mastrangelo A, Giani M, Groppali E, Castorina P, Soldà G, Robusto M, Fallerini C, Bruttini M, Renieri A, Montini G.
PMID: 33330536
Front Med (Lausanne). 2020 Nov 23;7:580376. doi: 10.3389/fmed.2020.580376. eCollection 2020.

No abstract available.

Showing 457 to 461 of 461 entries