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Research 451–480 of 1000+
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Female pattern hair loss
- Pseudofolliculitis barbae; current treatment options
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- Cutaneous immunopathology of androgenetic alopecia
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Fertility counseling and preservation: considerations for the pediatric endocrinologist
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Native and engineered extracellular vesicles for wound healing
- Tracing the developmental origin of tissue stem cells
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Combing the genome for the root cause of baldness
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Integrative analysis of Iso-Seq and RNA-seq data reveals transcriptome complexity and differential isoform in skin tissues of different hair length Yak
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Prevalence and treatment of Alopecia areata in Taif area, KSA
- Alopezien und Hypotrichosen im Kindesalter
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Prunus mira Koehne in Sichuan, China: Recorded History as a Medicine and Food, Modern Applications, Distribution, and Ethnobotanical Investigations
- Hypotrichosis with juvenile macular dystrophy
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment