Search
for
Sort by
Research 541–570 of 1000+
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Androgenic alopecia: an entity to consider in adolescence
- Animal models of human skin disease
- Electrophoretic analysis of human hair keratins
- New idea for hair transplantation to preserve more donor hair follicles
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Clinical characteristics and factors associated with different BASP subtypes of androgenetic alopecia
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- An Unusual Compulsive Behavior Related to Scalp Psoriasis and Hair Follicle Anxiety in Young Men
- The Role of Moracin M in Promoting Hair Growth: Insights into Mechanisms of WNT/β- Catenin Pathway Activation and Angiogenesis Enhancement in Human Dermal Papilla Cells
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Role of anti-miasmatic remedy in case of alopecia areata
- [Monilethrix is a hereditary hair shaft disorder].
- Allergen of the Month—Witch Hazel
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- FGF5 is a crucial regulator of hair length in humans
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Screening for gestational diabetes: usefulness of clinical risk factors
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- High-throughput sequencing of hair follicle development-related micrornas in cashmere goat at various fetal periods
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Diagnostic approach to low‐renin hypertension
- Promotion of anagen, increased hair density and reduction of hair fall in a clinical setting following identification of FGF5-inhibiting compounds via a novel 2-stage process
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats