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Research 811–840 of 1000+
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- <i>De novo</i> designed bifunctional proteins for targeted protein degradation
- Radiologie Aspects of Thallium Poisoning
- BH04 A hair-raising complication: <i>de novo</i> frontal fibrosing alopecia after transplantation
- Has the ISHRS changed the world of hair restoration?
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- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- Implication of allopregnanolone in the antinociceptive effect of N -palmitoylethanolamide in acute or persistent pain
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Hedgehog Signaling in Papillary Fibroblasts Is Essential for Hair Follicle Regeneration during Wound Healing
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Review of the 8th Congress of the Brazilian Association of Hair Restoration Surgery | July 27-30, 2022
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- KY19382, a novel activator of Wnt/β-catenin signaling, promotes hair re-growth and hair follicle neogenesis
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- Réparer ou régénérer,il faut choisir…
- Viable SARS-CoV-2 shedding under remdesivir and dexamethasone treatment
- Scalp-sparing total skin electron therapy in mycosis fungoides: Case report highlighting technique and outcome
- Transcriptome sequencing reveals the expression profiles of lncRNAs and mRNAs in goat skin tissues with different types of wool coats
- Safety and Efficacy of Oral administrated Cepharanthine in Non-hospitalized, asymptomatic or mild COVID-19 patients: A Double-blind, Randomized, Placebo-controlled Trial
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- III CONGRESSO MÉDICO ACADÊMICO UNIPAC-JF
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Progress in the Expression, Purification, and Characterization of Recombinant Collagen
- Development and Assessment of an Artificial Intelligence–Based Tool for Skin Condition Diagnosis by Primary Care Physicians and Nurse Practitioners in Teledermatology Practices
- How drug repurposing can advance drug discovery: challenges and opportunities
- The role of dermocosmetics in the management of cancer-related skin toxicities: international expert consensus
- Accurate quantification of minimal residual disease at day 15, by real-time quantitative polymerase chain reaction identifies also patients with B-precursor acute lymphoblastic leukemia at high risk for relapse
- Comments regarding “Hair regrowth during chemotherapy after scalp cooling technique”
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment