高度
发表于 2025-3-25 07:22:34
Evolving Genomics of Pulmonary Fibrosis,uch technologies have been applied to lungs and cells of patients and animal models of disease with the goal of identifying key molecules with a role in pathogenesis or to develop biomarkers of disease presence, progression, and outcome as well as to identify potential drug targets. Genomics profili
抵消
发表于 2025-3-25 09:23:38
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anthesis
发表于 2025-3-25 13:04:39
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感染
发表于 2025-3-25 17:16:37
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propose
发表于 2025-3-25 23:33:30
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Debrief
发表于 2025-3-26 01:12:50
Mimics of Idiopathic Pulmonary Fibrosis,te thoracic imaging, which in many cases may be sufficient to attain a confident diagnosis. In other cases, however, sampling of lung tissue might be necessary to confirm a usual interstitial pneumonia (UIP) histopathologic pattern if high-resolution computed tomography (HRCT) does not reveal a UIP
即席
发表于 2025-3-26 07:35:49
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Paraplegia
发表于 2025-3-26 09:33:23
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locus-ceruleus
发表于 2025-3-26 14:53:46
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营养
发表于 2025-3-26 18:42:03
Lung Transplantation for Idiopathic Pulmonary Fibrosis,to resolve fibrosis or improve lung function in IPF. Lung transplantation therefore remains the only lifesaving therapy available to treat patients with IPF. A shortage of suitable donor organs limits the number of affected individuals who can undergo this procedure, highlighting the need to allocat