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Research 31–60 of 1000+
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Stem cells and aberrant signaling of molecular systems in skin aging
- From hair colour to diagnosis
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Clinical report of a Holstein's calf with ichthyosis.
- The genetics of hair shaft disorders
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Androgen Biosynthesis and Gene Defects
- Genetic Hair Disorders: A Review
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- The genetic basis of dermatophytosis skin infection susceptibility
- [Visual field defect in a patient given sodium valporate then carbamazepine: possible effect of aminotransferase inhibition].
- Advances in genetic and molecular understanding of Omenn syndrome - implications for the future
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Vitamin D-dependent rickets type II. Defective induction of 25-hydroxyvitamin D3-24-hydroxylase by 1,25-dihydroxyvitamin D3 in cultured skin fibroblasts.
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Characterization of an autoimmune condition associated with AEC syndrome
- Molecular epidemiology of hypospadias: Review of genetic and environmental risk factors
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Woolly Hair in Two Siblings
- Acquired Structural Defects of the Hair
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.