Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sumana Kalyanasundaram"'
Autor:
Alfonso Schiavi, Eva Salveridou, Vanessa Brinkmann, Anjumara Shaik, Ralph Menzel, Sumana Kalyanasundaram, Ståle Nygård, Hilde Nilsen, Natascia Ventura
Publikováno v:
iScience, Vol 26, Iss 4, Pp 106448- (2023)
Summary: Excessive iron accumulation or deficiency leads to a variety of pathologies in humans and developmental arrest in the nematode Caenorhabditis elegans. Instead, sub-lethal iron depletion extends C. elegans lifespan. Hypoxia preconditioning pr
Externí odkaz:
https://doaj.org/article/718e9a6fdb4d42a78172e8de69e26027
Autor:
Alfonso Schiavi, Alessandra Runci, Eva Salveridou, Teresa Maiorino, Vanessa Brinkmann, Anjumara Shaik, Marta Barenys, Ellen Fritsche, Ralph Menzel, Sumana Kalyanasundaram, Ståle Nygård, Hilde Nilsen, Flavie Strappazzon, Natascia Ventura
Publikováno v:
SSRN Electronic Journal.
Autor:
Sumana Kalyanasundaram, Aina Elisabeth Fossum Moen, Colin Charnock, Hege Smith Tunsjø, Truls Michael Leegaard
Publikováno v:
APMIS. 126:533-537
Current clinical diagnostic procedures have shortcomings in the differentiation of Staphylococcus argenteus from Staphylococcus aureus. This article presents three cases of Staphylococcus argenteus obtained from clinical samples. The initial results
Autor:
Huiming Lu, Jane Tian, Jesse S. Kerr, David A. Sinclair, Tyler B. Waltz, Mark P. Mattson, Ravi Chand Bollineni, Sumana Kalyanasundaram, Morten Scheibye-Knudsen, Hilde Nilsen, Henok Kassahun, Marya Morevati, Qiping Lu, Wendy B. Iser, Raghavendra A. Shamanna, Jun Li, Mark A. Wilson, Deborah L. Croteau, Vilhelm A. Bohr, Evandro Fei Fang, Bradley N. Wollman, Krisztina Marosi
Publikováno v:
Cell Metabolism. 24:566-581
Ataxia telangiectasia (A-T) is a rare autosomal recessive disease characterized by progressive neurodegeneration and cerebellar ataxia. A-T is causally linked to defects in ATM, a master regulator of the response to and repair of DNA double-strand br
Autor:
Merete Molton Worren, Sumana Kalyanasundaram, Aina Elisabeth Fossum Moen, Truls Michael Leegaard, Hege Smith Tunsjø
Publikováno v:
European Journal of Clinical Microbiology & Infectious Diseases. 36:65-74
Rapid nucleic acid amplification tests for methicillin-resistant Staphylococcus aureus (MRSA) diagnostics commonly target the mec resistance gene, genes specific for S. aureus, and the integration site for the SCCmec resistance cassette, orfX. Due to
Autor:
Evandro Fei, Fang, Henok, Kassahun, Deborah L, Croteau, Morten, Scheibye-Knudsen, Krisztina, Marosi, Huiming, Lu, Raghavendra A, Shamanna, Sumana, Kalyanasundaram, Ravi Chand, Bollineni, Mark A, Wilson, Wendy B, Iser, Bradley N, Wollman, Marya, Morevati, Jun, Li, Jesse S, Kerr, Qiping, Lu, Tyler B, Waltz, Jane, Tian, David A, Sinclair, Mark P, Mattson, Hilde, Nilsen, Vilhelm A, Bohr
Publikováno v:
Cell metabolism. 24(4)
Ataxia telangiectasia (A-T) is a rare autosomal recessive disease characterized by progressive neurodegeneration and cerebellar ataxia. A-T is causally linked to defects in ATM, a master regulator of the response to and repair of DNA double-strand br