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90-120 / 1000+ resultsresearch Rational Design and Synthesis of 4-((1R,2R)-2-Hydroxycyclohexyl)-2(trifluoromethyl)benzonitrile (PF-998425), a Novel, Nonsteroidal Androgen Receptor Antagonist Devoid of Phototoxicity for Dermatological Indications
PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.
research Message from the Chair of the Pro Bono Committee
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research 17beta Hydroxysteroid Dehydrogenase Type 3 Inhibitors
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research Outgoing ABHRS President’s Corner
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research Megatransplants in Transition: A Pictorial Review
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research Gestational safety: No time for a pregnant pause
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research Phase I Study of the Hedgehog Pathway Inhibitor IPI-926 in Adult Patients with Solid Tumors
The drug IPI-926 is safe at 160 mg daily and may help treat certain tumors, especially basal cell carcinoma.
research Editor's notes
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research 0196 Levamisole-induced pyoderma gangrenosum case report
research 710 BIOMARKERS OF SUNITNIB CLINICAL RESPONSE IN METASTATIC RENAL CLEAR CELL CARCINOMA PATIENTS
research ISHRS: Expanding FUE Education
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research Solid-Phase Microextraction and Related Techniques in Bioanalysis
research 549 Temporary cell cycle arrest in human scalp hair follicles and their epithelial stem cells by ALRN-6924: A novel strategy to selectively protect p53-wildtype cells against paclitaxel-induced alopecia
ALRN-6924 may prevent hair loss caused by chemotherapy.
research 52252 Analysis of basal cell carcinoma and trichoepithelioma with digital spatial profiling
research Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
A Chinese man with KID syndrome had a new mutation in the GJB2 gene.
research 267 Single- and multiple-ascending dose studies of DS-2325a, a KLK5 inhibitor for the treatment of Netherton syndrome
DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.
research A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.
research Editor's notes
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research Kudos
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research Notes from the Editor Emeritus
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research Natural Transplants, Hair Transplantation Clinic. Hairstyles For Alopecia Sufferers near West Palm Beach Call (844) 327-4249.
research 0416 Involvement of calcinosis cutis in autoimmune connective tissue diseases
research Chromatographic Method for Simultaneous Quantification of Gemcitabine and Olaparib Recovered from Isolated Pancreatic Tissue
A reliable method was developed to measure gemcitabine and olaparib in pancreatic tissue, aiding pancreatic cancer treatment.
research Contents Vol. 231, 2015
The document covers various dermatological treatments and conditions.
research Doxazosin + finasteride in BPH with TPV ??? 25mL
research Issue Information
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research Error in Author Surname
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research Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.
research CSI on steroids
Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.