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Research 391–420 of 1000+
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Intercellular junctions in normal epidermis
- Epidermal patterning and induction of different hair types during mouse embryonic development
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth?
- Ichthyosis with confetti: clinics, molecular genetics and management
- Androgens and Hirsutism in a Large Cohort of Portuguese Women
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Association of Acne Tarda with Endocrinological Disorders
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study