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Research 181–210 of 1000+
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Making the head: Caspases in life and death
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- The clinical spectrum of parathyroid disease
- Darier Sign: A Historical Note
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Hair loss in children.
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- The Spectrum of Skin Disease Among Indian Children
- Morphological Approach to Hair Disorders
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Identification of the cell lineage at the origin of basal cell carcinoma
- Acquired Uncombable Hair
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light
- Hair That Is Difficult to Manage in a Hispanic Girl
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Westwood Carolina Conference on Clinical Dermatology
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Disorders of hair
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Disorders of the skin appendages
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Hair Disorders
- Hormone replacement therapy and the skin
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- 190 A cross-sectional study evaluating skin, hair, nail and bone disease in patients with focal dermal hypoplasia