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Research 661–690 of 1000+
- Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with <i>AIRE</i> gene mutation (autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy, APECED syndrome) treated with ruxolitinib
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Parallels in signaling between development and regeneration in ectodermal organs
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"
- Neural Potential of a Stem Cell Population in the Hair Follicle
- Prenatal hair development: Implications for drug exposure determination
- Ichthyosis with confetti: clinics, molecular genetics and management
- Multipotent Nestin-Positive Stem Cells Reside in the Stroma of Human Eccrine and Apocrine Sweat Glands and Can Be Propagated Robustly In Vitro
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Ulerythema Ophryogenes
- Msx2 Supports Epidermal Competency during Wound-Induced Hair Follicle Neogenesis
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- Clinical Case Notes. Propecia-associated bilateral cataract
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Organizational principles of integumentary organs: Maximizing variations for effective adaptation
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Progress in Relevant Growth Factors Promoting the Growth of Hair Follicle
- Expression ofWise in chick embryos
- What Syndrome Is This?
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Using High-Throughput Immunoblotting to Identify Proteins Involved in the Differentiation of ES Cells along the Hair Follicle Lineage in Vitro
- Two cases of aplasia cutis congenita with hair collar signs and macrophage hyperplasia
- Understanding skin morphogenesis across developmental, regenerative and evolutionary levels
- Alopecia in Cronkhite-Canada syndrome
- The amazing miniorgan: Hair follicle