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Research 31–60 of 1000+
- 4. Bullous/Mucous Membrane
- JAK-centric explainable few-shot gene-expression diagnosis framework for alopecia via MultiPLIER priors and relation-style set-to-set comparison
- Next generation human skin constructs as advanced tools for drug development
- The Rotterdam Study: 2016 objectives and design update
- Chronic overlapping pain conditions and nociplastic pain
- Drug repurposing: A novel strategy to target cancer stem cells and therapeutic resistance
- Treatment Strategies for Cutaneous and Oral Mucosal Side Effects of Oncological Treatment in Breast Cancer: A Comprehensive Review
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Two parietal cephaloceles in a female neonate
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Alopecia: Association with Resistance to Thyroid Hormones
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Scarless wound healing – a literature review
- Congenital atrichia and hypotrichosis
- Visual Diagnosis: An Adolescent Female Who Has Increasing Hair Growth
- Amplicon-based sequencing and co-occurence network analysis reveals notable differences of microbial community structure in healthy and dandruff scalps
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Transcriptomic analyses of regenerating adult feathers in chicken
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- Polycystic ovary syndrome
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2