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Research 181–210 of 1000+
- A catena between psychiatric disorders and non‐scarring alopecias—A systematic review
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- The molecular basis of human keratin disorders
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Harnessing miRNA Milk-Derived Exosomes for Hair Loss Disorders: In Vitro Modulation of WNT Signaling and Dermal Papilla Proliferation
- The Dickkopf Protein Family in Non-Neoplastic Disorders: Emerging Roles and Therapeutic Targeting
- Clinical Evaluation of Cactus (Cereus Grandiflorus) Enriched Hair Oil for Hair Fall Disorders
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Exosomes: A Promising Strategy for Repair, Regeneration and Treatment of Skin Disorders
- Ulerythema Ophryogenes
- A perspective on predictive markers of alopecia
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Characterization of an autoimmune condition associated with AEC syndrome
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- GRowing an Epidermal Tumor
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- The Roles of EDA2R in Ageing and Disease
- Alopecia in preexisting autoimmune thyroid disease in family medicine practice: can hyperprolactinemia induce hair loss? A case report
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Investigating the roles of cellular senescence in embryogenesis and aging
- A Case of Cronkhite-Canada Syndrome Involving the Entire Gastrointestinal Tract
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation