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Research 361–390 of 1000+
- Genetic Hair Disorders: A Review
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Ulerythema Ophryogenes
- Hair and Nail Relationship
- Msx2 Supports Epidermal Competency during Wound-Induced Hair Follicle Neogenesis
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling
- Genetics of Structural Hair Disorders
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Hair shaft disorders in children – An update
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermatopathology and molecular genetics
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital atrichia and hypotrichosis
- 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
- Progress in Relevant Growth Factors Promoting the Growth of Hair Follicle
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Disorders of the Hair and Scalp in Children
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- What Syndrome Is This?