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Research 451–480 of 1000+
- 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
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Congenital adrenal hyperplasia
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- 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
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Male androgenetic alopecia (Part II)
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Investigating the Safety and Efficacy of Platelet-Rich Plasma (PRP) Treatment for Female Androgenetic Alopecia: Review of the Literature
- 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
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Function of KLF4 in Stem Cell Biology
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- How a Bird Gets Its Feathers: Insights from Chromatin Looping
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Design and development of cosmeceutical cream for hyperpigmentation and anti-aging
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Combined activity of selenite-resistant bacteria and Pisum sativum sprout extract against Malassezia furfur: A preliminary qualitative evaluation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Ayurvedic Approach in Management of Vata-Kaphaja Artavdushti (PCOS)
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant