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Research 391–420 of 1000+
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance
- Epidermal Deletion of Rac1 Causes Stem Cell Depletion, Irrespective of whether Deletion Occurs during Embryogenesis or Adulthood
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria
- YAP1 promotes adipogenesis by regulating the negative feedback mechanism of the Hippo signaling pathway via LATS2
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Androgen Receptor Actions Modify Skin Structure and Chemical Carcinogen-induced Skin Cancer Susceptibility in Mice
- Diagnostic approach to low‐renin hypertension
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- The ITGB6 gene: its role in experimental and clinical biology
- A curated catalog of canine and equine keratin genes
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Testosterone Treatment in Women – An Overview
- Le gène<i>hairless</i>de la souris
- 202 Activation of breast cancer cell proliferation by ROR-alpha through aromatase promoter
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Prolactin: an emerging force along the cutaneous–endocrine axis
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- AIMP1-Derived Peptide Secreted from Hair Follicle Stem Cells Promotes Hair Growth by Activating Dermal Papilla Cells