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Research 91–120 of 365
- A spermidine-based nutritional supplement prolongs the anagen phase of hair follicles in humans: a randomized, placebo-controlled, double-blind study
- Diseases of Periocular Hair
- Hair loss and its management in children
- Marie-unna hereditary hypotrichosis
- Le gène<i>hairless</i>de la souris
- Selected topics in pediatric hair loss
- Alopecia Areata and Alopecia Areata Incognita
- Diagnostic challenges in determining alopecia areata
- The Role of Histone Demethylases in Disease
- Alopecia and Its homoeopathic treatment
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Contents Vol. 4, 2018
- Alopecia and Thyroid Disease
- Thyroid hormone action on skin
- Congenital hair loss disorders: Rare, but not too rare
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Thyroid hormone action on skin.
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Micronutrients for Hair and Nails
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- Ichthyosis Follicularis With Alopecia and Photophobia
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA