ANTH 发表于 2025-3-28 14:41:56
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Muscular Dystrophy: Underlying Cellular and Molecular Mechanisms and Various Nanotherapeutic Approaoth dominant and recessive and can be autosomal or X-linked. These disorders are marked by gradual muscle degeneration and diminished muscle potency of variable severity depending on the stage and onset age of the disease, as well as the distribution of affected muscles. In most cases, patients ultiCRAMP 发表于 2025-3-28 23:05:52
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,Alterations in Receptor Genes in Huntington’s Disease,genes in HD are investigated, with a specific focus on the role of these genes in the disease and the receptors that are altered. Receptor genes play a crucial role in HD by encoding proteins involved in cellular signal transduction. Dysfunction in these receptors can disrupt normal cellular activit新娘 发表于 2025-3-29 08:12:12
Genetic Modulators in Amyotrophic Lateral Sclerosis,e loss of motor neurons in the cortical, spinal cord, and brainstem regions. This neuronal death leads to paralysis and, in later stages, respiratory failure, often resulting in death. The incidence of ALS is relatively low, with around 1–2 people approx. per 100,000 annually and life expectancy forAstigmatism 发表于 2025-3-29 14:59:28
Modulators and Poststroke Behavioral Changes,l necrosis, a dynamic and complex event. Stroke ranks third in terms of disability-adjusted life years and this condition is the second major cause of mortality. The cerebral vasculature, an important target of oxi-inflammatory stress-driven biomolecular degradation, is interestingly playing a signiopportune 发表于 2025-3-29 17:05:10
,Presynaptic Dysfunction in Parkinson’s Disease,These signs are brought on by dopamine neuronal deprivation in the substantia nigra of the brain. The drugs available will lessen the symptoms but the advancement of the disease cannot be ceased. Different studies manifested that synaptic dysfunction and degradation of axons take place earlier than动机 发表于 2025-3-29 21:58:43
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