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Research 901–930 of 1000+
- Australasian Society for Dermatology Research Meeting, May 2006
- This Month in the Journal
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Clinical Snippets
- The Editor's Choice
- Table 1_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Clinical Snippets
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- The Agouti Gene in Obesity: Central and Peripheral Mechanisms, and Therapeutic Implications
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Natural potent androgens: Lessons from human genetic models
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Molecular basis of congenital atrichia in humans and mice.
- News in brief
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Cystatin M/E Is a High Affinity Inhibitor of Cathepsin V and Cathepsin L by a Reactive Site That Is Distinct from the Legumain-binding Site
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Hypotrichosis with juvenile macular dystrophy
- Le mélanome malin bilatéral de l'uvée
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- TON1 recruiting motif 21 positively regulates the flavonoid metabolic pathway at the translational level in Arabidopsis thaliana
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case