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Research 751–780 of 1000+
- PCSK9: From Nature’s Loss to Patient’s Gain
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A kindred with mutant IKAROS and autoimmunity
- Nilotinib-Induced Keratosis Pilaris
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- 603 Pathological modeling of epidermolysis bullosa simplex (EBS) using induced pluripotent stem cells (iPSC)
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Exploring the Dermoscopic Patterns in Tuberous Sclerosis
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- Tricholemmoma and tricholemmal carcinoma and Cowden syndrome
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Congenital atrichia associated with situs inversus and mesocardia
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Ectodermal Dysplasia: Variable Expressions
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Linear trichoepithelioma on the neck of a 15-year-old girl
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”
- Hair follicle-specific keratins and their diseases
- Myotonic Dystrophy—A Progeroid Disease?