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Research 691–720 of 1000+
- 4th Intercontinental Meeting of Hair Research Societies 2004 The "World of Hair"
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Rheumatoid arthritis and gouty arthritis in an adult patient with Down's syndrome
- Congenital Adrenal Hyperplasia
- The Molecular Basis of Androgen Insensitivity
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- DNA Damage, Checkpoint Responses, and Cell Cycle Control in Aging Stem Cells
- A Case of Relapsed Leprosy Successfully Treated With Sparfloxacin
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- 5-Alpha reductase deficiency
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Generalised Glucocorticoid Resistance
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- <i>Hoxc13</i> mutant mice lack external hair
- The PDGF/PDGFR pathway as a drug target
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments
- Keratin disorders: from gene to therapy