Lv4
510 积分 2025-03-04 加入
Journey toward unraveling the molecular basis of hereditary hair disorders
9天前
已完结
N-Terminal 5-Mer Peptide Analog P165 of Amyloid Precursor Protein Repairs Skin Photodamage Induced by UVB through the Nrf2 Signaling Pathway
25天前
已完结
Pan-cancer prediction of radiotherapy benefit using genomic-adjusted radiation dose (GARD): a cohort-based pooled analysis
26天前
已完结
Focal Acral Hyperkeratosis: A Rare Cutaneous Disorder within the Spectrum of Costa Acrokeratoelastoidosis
1个月前
已完结
Acrokeratoelastoidosis and knuckle pads coexisting in a child
1个月前
已关闭
Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
1个月前
已完结
A Novel Missense Mutation, A118E, in the Helix Initiation Motif of the Type II Hair Cortex Keratin hHb6, Causing Monilethrix
1个月前
已完结
Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
1个月前
已完结
Molecular analysis of an extended Palestinian family from Israel with monilethrix
1个月前
已完结
Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
1个月前
已完结
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