Search
for
Sort by
Research 301–330 of 1000+
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Fibroblast growth factor 5-short (FGF5s) inhibits the activity of FGF5 in primary and secondary hair follicle dermal papilla cells of cashmere goats
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- How to diagnose a lipodystrophy syndrome
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- The Basic Science of Hair Biology
- Dietary isoflavone increases insulin-like growth factor-I production, thereby promoting hair growth in mice
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Evolution of Trichocyte Keratins
- Glucocorticoid and Sex Hormone Receptors: Clinical Implications and Therapeutic Relevance
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Neuroactive Steroids and Ethanol Exposure: Relevance to Ethanol Sensitivity and Alcohol Use Disorders Risk
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Uncombable hair improved by biotin
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- 200 The relationship between the expression of cytokeratin 5/6 and clinicopathologic factors in invasive breast carcinoma
- 202 Activation of breast cancer cell proliferation by ROR-alpha through aromatase promoter
- Cutaneous signals of immune system disease
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Recently Identified Forms of Epidermolysis Bullosa
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals