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Research 721–750 of 1000+
- Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata
- Ether: Fiction or Reality? A Review
- Approach to Alopecia in Dogs in Clinical Practice
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Painful thickened skin on the soles of the feet
- A Clinical Study of Androgenetic Alopecia (V)
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Oral Presentations
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Emerging interactions between skin stem cells and their niches
- Hairy tale of signaling in hair follicle development and cycling
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- The neurosteroidogenic enzyme 5α-reductase modulates the role of D1 dopamine receptors in rat sensorimotor gating
- Development of gene therapy for inner ear disease: Using bilateral vestibular hypofunction as a vehicle for translational research
- Light Microscopic Hair Abnormalities in Children: Retrospective Review of 119 Cases in a 10-Year Period
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Abstracts of 42nd National Conference of Association of Clinical Biochemists of India (ACBICON 2015)
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- News in brief
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Adult Onset Isolated Hypogonadotropic Hypogonadism- a Cause of Secondary Amenorrhea
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- A newborn presenting with congenital blistering