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Research 151–180 of 1000+
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- <i>WNT10A</i> , dermatology and dentistry
- How to diagnose a lipodystrophy syndrome
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Monilethrix
- Author response: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Characterization of Human Keratin-Associated Protein 1 Family Members
- Uncombable hair syndrome and beyond
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- A woman with iatrogenic androgenetic alopecia responding to finasteride
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Alopecia: Association with Resistance to Thyroid Hormones
- An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- Clinical Impact of Molecular Diagnostics in Endocrinology
- Woolly Antics between the Sheaths
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Remodelling of cytoskeleton and plasma membrane proteins contributes to drought sensitivity of Arabidopsis<i>rhd2</i>mutant