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Research 661–690 of 1000+
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- 3D cell culture stimulates the secretion of in vivo like extracellular vesicles
- PINK1 deficiency rewires early immune responses in a mouse model of Parkinson’s disease triggered by intestinal infection
- BMI1 is required for melanocyte stem cell maintenance and hair pigmentation
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Visualization of individual cell division history in complex tissues
- <i>Microsporum gypseum</i> isolated from a feline case of dermatophytosis
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Wounds and the Microbiota: The Healing Interplay Between Host and Microbial Communities
- Scalp Infection Caused by Mycobacterium abscessus Manifested as Patchy Alopecia in an Immunocompetent Female
- The urine as a diagnostic key for a homozygous EGFR mutation
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Abstracts
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Keep your hair on
- Follicles, fungi and scalp conditions
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- A stretch-responsive fibroblast program promotes epidermal stem cell self-renewal during skin expansion
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- TYK2 Inhibition with Deucravacitinib Improves Clinical Outcomes and Resolves Interferon-Driven Inflammation in Lichen Planopilaris
- Epigenetic and transcriptional profiling of secondary hair follicle stem cells during cashmere growth
- Association of prior 5-α-reductase inhibitor exposure with ICI benefit in metastatic RCC: Multicentre cohort with single-cell immune profiling.
- A Multimodal Approach to Facial Rejuvenation—Integrating HA Fillers, Collagen Stimulators, Botulinum Toxin and Energy-Based Devices for Optimal Patient Outcomes