Search
for
Sort by
Research 511–540 of 1000+
- <i>Hoxc13</i> mutant mice lack external hair
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Endocrine Influences on Hair Growth
- Hair shaft disorders
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Congenital atrichia and hypotrichosis
- Australasian Society for Dermatology Research Meeting, May 2006
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- Congenital adrenal hyperplasia
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Nonclassic adrenal hyperplasia
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Diagnostic approach to low‐renin hypertension
- Biotinidase deficiency characterized by skin and hair findings
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology