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Research 841–870 of 1000+
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Effect of Platelet-Rich Plasma (PRP) on Dermal Skin Flap Survival: An Experimental Study in Rats
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Multiple facial atrophic scars in childhood
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- A BIOCHEMICAL MARKER IN A DOMINANT MOUSE TRAIT
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome