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Research 631–660 of 860
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Expression and localization of Artemis serine 516 phosphorylation in human scalp skin
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- The exploration of mitochondrial‐related features helps to reveal the prognosis and immunotherapy methods of colorectal cancer
- TRPV3 Ion Channel: From Gene to Pharmacology
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Immunostaining study of cytokeratins in human hair follicle development
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Ehlers-Danlos syndrome: From bedside to bench
- Lrig1-expressing epidermal progenitors require SCD1 to maintain the dermal papilla niche
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Monilethrix – Case report of a rare disease
- The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits
- Nutritional Disorders of the Hair and Their Management
- Ernährungsstörungen des Haares und deren Management
- Betaine supplementation is less effective than methionine restriction in correcting phenotypes of CBS deficient mice
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- The Roles of EDA2R in Ageing and Disease
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin