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Research 961–990 of 1000+
- Integrating whole-genome re-sequencing and transcriptome data to reveal the molecular mechanism of TBX5 gene regulating feathered feet in Guangxi native chickens
- Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy
- Familial Occurrence of Eruptive Vellus Hair Cysts
- Existence of various structural zones in keratinous tissues revealed by X-ray microdiffraction
- Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain
- Rooster feathering, androgenic alopecia, and hormone-dependent tumor growth: What is in common?
- Atrichia With Papular Lesions
- William Harvey and the Discovery of the Circulation of the Blood
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease
- Overcoming emotional struggles and alopecia totalis: homeopathic healing at Dr. Batra’s
- Biotechnology of functional proteins and peptides for hair cosmetic formulations
- The structure of people’s hair
- Structural and Immunocytochemical Characterization of Keratinization in Vertebrate Epidermis and Epidermal Derivatives
- Review: Evolution and diversification of corneous beta‐proteins, the characteristic epidermal proteins of reptiles and birds
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- Family History and Risk of Hair Loss
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Genes for Hair and Avian Keratins
- Dr Shoji Okuda (1886-1962): The great pioneer of punch graft hair transplantation
- Kerion
- Albert kligman, also a hair man
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Keratin 75 Is a Component of the LINC Complex and Has an Essential Role in Mediating the SOX2 Rapid Healing Response during Wound Repair
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Misspelling of Coauthor Surname
- Isolated long white eyelash: An underrecognized trichologic finding
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- [Translated article] Frontal Fibrosing Alopecia and Lichen Planus Pigmentosus: Variants of the Same Disease?