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Research 421–450 of 447
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- On Telogen Effluvium
- The Excesses of Cosmetic Medicine
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- The Historical Studies Underpinning the Concept of Hair Follicle Neogenesis
- Author response: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Decision letter: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- A Cluster of (Old) Portuguese Derivational Suffixes:<i>-ece, -ice, -ez(a),</i>Viewed in Relation to their Spanish Counterparts
- Proteome Analysis of Human Hair Shaft
- Controlled Delivery of T-box21 Small Interfering RNA Ameliorates Autoimmune Alopecia (Alopecia Areata) in a C3H/HeJ Mouse Model
- Genetically separable determinants of hair keratin gene expression
- Social Media in Dermatology and an Overview of Popular Social Media Platforms
- Diagnosis and management of primary hypothyroidism in Traditional Chinese Medicine (TCM) and Traditional Indian Medicine (Ayurveda)
- 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>)
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia