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research A Proposal from Steven C. Chang, MD
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research Promotion of Skin Carcinogenesis by Dimethylarsinic Acid in Keratin (K6)/ODC Transgenic Mice
Dimethylarsinic acid speeds up skin tumor growth in certain mice.
research LB918 Analysis of National Inpatient Sample to characterize admissions for pediatric patients with dystrophic epidermolysis bullosa
Pediatric patients with dystrophic epidermolysis bullosa face more hospital admissions, procedures, and complications than others.
research 519 Phase I/IIa clinical trial for recessive dystrophic epidermolysis bullosa using genetically corrected autologous keratinocytes
The gene therapy showed significant wound healing and was safe for treating severe RDEB.
research Index
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research Index
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research MICROBIAL OXIDATION OF FINASTERIDE WITH MACROPHOMINA PHASEOLINA(KUCC 730)
research My Thoughts…
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research Pioneer’s Page
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research Message from the 2016 Surgical Assistants: Program Vice Chair
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research Mutation in 5′ upstream region of GCH I gene causes familial dopa-responsive dystonia
A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.
research 43755 Rapid Reduction and Strict Complete Response in Itch With Oral Difelikefalin in Subjects With Notalgia Paresthetica and Moderate-to-Severe Pruritus
Oral difelikefalin significantly reduces itch in notalgia paresthetica.
research 575 Senescent atrophic epidermis retains Lrig1+ stem cells and loses Wnt signaling, a phenotype shared with CD44KO mice
research Correction
research Correction
research Publications from Juntendo University Graduate School of Medicine, 2018 [1/6]
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research Editorial Comments
research We Salute You, Mr. Paek
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research 0955 Selective BET inhibition as potential hidradenitis suppurativa treatment
research Outgoing ABHRS President’s Corner
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research Atrophic Diseases of the Adnexa
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research Hair disorders
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research Throwing Caution to the Wind?
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research Case Report: Arteriovenous Fistula
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research A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.
research Supplementary figure S2
research Follow-up
research A review of HAIRCON 2011
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