Search
for
Sort by
Research 751–780 of 1000+
- Assessment of scalp hair survivin in patients with premature greying of hair
- Phylloid terminal hair nevus: A unique clinical entity
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Comparison of allogeneic stem cell transplant conditioning regimens in AML, MDS and CLL
- Genetic Defects of Female Sexual Differentiation
- Transsexualism
- Modelling androgen synthesis and action during human sexual differentiation
- American Academy of Dermatology
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Genetic prediction of male pattern baldness
- Interferon in the treatment of cutaneous T-cell lymphoma
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Wnt signaling in skin organogenesis
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Significance of the S100A4 Protein in Psoriasis
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Hair Restoration Surgery: The State of the Art
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Male androgenetic alopecia (Part II)
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Hormonal, Medical, and Nonsurgical Aspects of Gender Affirmation
- Function of KLF4 in Stem Cell Biology