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Research 181–210 of 1000+
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Androgenetic alopecia
- The efficacy and safety of valproic acid medications with controlled active ingredient release in adults in real clinical practice from the position of pharmacokinetic and pharmacogenetic approaches
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Developmental origin of polycystic ovary syndrome - a hypothesis
- Epidermal stem cell diversity and quiescence
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse
- Defining compartmentalized stem cell populations with distinct cell division dynamics in the ocular surface epithelium
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Mosaic Hair Regrowth Pattern of Ophiasis and Androgenic Alopecia in a Patient With Alopecia Areata Totalis
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Diagnosis and treatment of trichotillomania
- Alopecia Areata Barbae in a Nutshell
- Treatment of Lipodystrophy with Troglitazone
- INNOVATIVE APPROACH TO CRC PREVENTION: THE ROLE OF LOW-PENETRATION GENES
- Notes from the Editor Emeritus
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Structure of human type II 5 alpha-reductase gene.
- Ubiquity and Diversity of Human-Associated Demodex Mites
- In search of decoding the syntax of the bioelements in human hair – A critical overview