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Research 181–210 of 1000+
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- WNT10B (wingless-type MMTV integration site family)
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Survival Skills for Doctors and their Families
- Microscopic Study concerning Hair Form of One Family in the Mixed Blood between European and Ponapean
- The roles of hepatocyte growth factor family members in androgen-regulation of human hair growth. A comparison of the expression of hepatocyte growth factor family members, HGF and MSP, and their receptors, c-Met and RON, in isolated hair follicles from normal and androgenetic alopecia (balding) scalp.
- PROFILE OF ALOPECIA AREATA: A QUESTIONNAIRE ANALYSIS OF PATIENT AND FAMILY
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Concerted gene duplications in the two keratin gene families
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- A Unique Type I Keratin Intermediate Filament Gene Family is Abundantly Expressed in the Inner Root Sheaths of Sheep and Human Hair Follicles
- Differential Expression of Genes Encoding a Cysteine-Rich Keratin Family in the Hair Cuticle
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Tourniquet syndrome: Interest of a systematic analysis of families’ social conditions to detect neglect situations
- Medicinal Value of Three Agricultural Weed Species of the Asteraceae Family: A Review
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Structure and hair follicle-specific expression of genes encoding the rat high sulfur protein B2 family
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome