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Research 121–150 of 1000+
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Aromatase deficiency in a male patient - Case report and review of the literature.
- 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
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Tsukushi is involved in the wound healing by regulating the expression of cytokines and growth factors
- A curated catalog of canine and equine keratin genes
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- No improvement in male-pattern hair loss using laser hair-comb therapy: a 6-month, half-head, assessor-blinded investigation in two men
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- Androgen receptor CAG repeat length is associated with ovarian reserve but not with ovarian response
- Absorption of Excess Selenium and Sulfur by Plants and Animals
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Atypical Pediatric Presentation of Pilomatricoma
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- Generalised Glucocorticoid Resistance
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Erosive Pustular Dermatosis of the Scalp Due to Afatinib: A Rare Case
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Androgen receptor gene polymorphism and biological age markers in men
- Virilizing insulinoma
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances