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Research 661–690 of 1000+
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Congenital Adrenal Hyperplasia
- Nonclassic congenital adrenal hyperplasia
- Keratin disorders: from gene to therapy
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Werner′s syndrome
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Editors' Picks
- Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change
- Role of caffeine in the management of androgenetic alopecia
- Full investigation of patients with polycystic ovary syndrome (PCOS) presenting to four different clinical specialties reveals significant differences and undiagnosed morbidity
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Creatine phosphokinase levels and isotretinoin therapy
- Delving into diversity: exploring different risk factors of premature greying of hair
- Diabetes, ovarian tumor, hyperparathyroidism, and papillary cancer: A chance association?
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- Adams–Oliver syndrome: new evidence in variable expressivity?
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia