Search
for
Sort by
Research 301–330 of 1000+
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Neural Potential of a Stem Cell Population in the Hair Follicle
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- 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
- Atrichia With Papular Lesions
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Ectodysplasin research—Where to next?
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Ulerythema Ophryogenes
- Msx2 Supports Epidermal Competency during Wound-Induced Hair Follicle Neogenesis
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- Dermatopathology and molecular genetics
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Clinical Case Notes. Propecia-associated bilateral cataract
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Hair loss among a group of Egyptian children
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Organizational principles of integumentary organs: Maximizing variations for effective adaptation
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- The fundamentals of WNT10A
- Progress in Relevant Growth Factors Promoting the Growth of Hair Follicle
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família