Faiza Iram, Ayesha Aiman, Luqman Ahmad Khan et al.
· Elsevier eBooks · 0 citations
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Archaea represent one of the three domains of cellular life and yet account for fewer than 1% of experimentally determined protein structures, leaving the extent of their structural novelty unknown. Here we present a systematic domain-level classification of 124,075 proteins from 65 archaeal classes spanning 21 phyla a...
R. Dustin Schaeffer, Jimin Pei, Rui Guo et al.
· PLoS Computational Biology · 0 citations
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Tapobrata Lahiri, Rajkrishna Mondal
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This paper estimates the savings in agricultural land area that would occur in Canada if all domestically-produced and consumed animal food products (AFPs) and fish were replaced with domestically-produced high-protein plant food products (PFPs), accompanied by increases in consumption of domestically-produced fruits a...
L. D. Danny Harvey
· Environmental Research: Food... · 0 citations
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This study aimed to construct an artificial neural network (ANN) diagnostic model for rheumatoid arthritis (RA) based on a neutrophil inflammation- and cell death-associated gene signature derived from a previously reported neutrophil extracellular traps (NETs)-related gene set, and to explore its association with immu...
Chun-Song Gu, Yu-Jia Chen, Wei Huang et al.
· Medicine · 0 citations
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Second-generation AOH analogues with enhanced pharmacological properties were created through scaffold optimization, and both compounds induced robust G2/M arrest at lower concentrations than the parent molecule and significantly enhanced transcription–replication conflicts in pancreatic cancer cells.
Pouya Haratipour, Maryam Zangi, Long Gu et al.
· Journal of Medicinal Chemist... · 0 citations
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This review delineates CCT6A’s multifunctional roles in oncogenesis and immune-metabolic dysregulation, critically evaluates its biomarker potential, and proposes targeted therapeutic frameworks to refine precision medicine paradigms across diverse disease landscapes.
Rui-Hang Du, Yi Cheng, Zi-Peng Ren et al.
· Molecular Biology Reports · 0 citations
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Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant neuropathy classically caused by a heterozygous deletion of the 17p11.2-p12 region encompassing PMP22. However, PMP22 sequence variants can produce HNPP-like or overlapping phenotypes, complicating variant interpretation. This narr...
Huan Li, You-Ping Wang, Cai-Xia Zhang et al.
· Frontiers in Neurology · 0 citations
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J. Devenport, C. Jennings, J. Kenealey et al.
· Journal of the Academy of Nu... · 0 citations
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Alpana Srishti Rai, Seneha Santoshi, Shazia Rashid
· Elsevier eBooks · 0 citations
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Shubhi Singh, Rudrani Rath, Sushma Jeyaraj et al.
· Elsevier eBooks · 0 citations
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Mahesh Narayan
· Elsevier eBooks · 0 citations
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