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Research 541–570 of 1000+
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- A Newborn With Hair Loss
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- A New CARASIL Family: Recurrent Lobar Hemorrhage as a Novel Characteristic of the Disease
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- LB1007 Systemic treatment with a KLK5 inhibitor shows efficacy in a murine model of Netherton syndrome
- The Naked (N) Mutation, Chromosome 15
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- Claudin tight junctionwhat's your function? The role of Claudin 6 in epidermal and hair follicle differentiation
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Analysis of differentially expressed genes of dermal papillae cells with aggregative behavior in uitro
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population