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Research 571–600 of 1000+
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currents
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- A Neonate with Blisters
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- 420 Severe thiopurine-induced myelotoxicity and hair loss in Japanese patients with NUDT15 gene variant: A retrospective case-control study
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development
- An unusual presentation of X-linked adrenoleukodystrophy
- Does Nicastrin Inadequacy Cause Melanocytotoxicity in Human Skin as in the Fish Counterpart?
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Hair Follicle Immune Privilege Revisited: The Key to Alopecia Areata Management
- The Okuda Papers: an extraordinary - but unfortunately unrecognized - piece of work that could have changed the history of hair transplantation
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Learning from nudity: lessons from the nude phenotype
- The character “hairless” in the mouse
- Skin manifestations among<i>GATA2</i>-deficient patients
- Tsukushi is involved in the wound healing by regulating the expression of cytokines and growth factors
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations