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Research 361–390 of 1000+
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Expert Opinion: Migraine, Psychiatric Comorbidities, and Treatment
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Systemic Autoimmune Diseases
- Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences
- Expert consensus on the management of androgenetic alopecia in India
- A newborn presenting with congenital blistering
- Monilethrix in three generations
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Mechanisms of aluminium toxicity, tolerance and amelioration in wheat
- Discreet monilethrix: De novo mutation on the example of polish families
- 5α-Reductase underscores the development of pectoral fin breeding tubercles in zebrafish
- Evolution of long scalp hair in humans
- Loose Anagen Hair Syndrome in an Indian Child with Trichoscopic Features
- Forensic DNA Phenotyping
- Tackling underrepresentation to aid understanding of Parkinson’s disease: Progress and further opportunities
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Decision letter: Selective amputation of the pharynx identifies a FoxA-dependent regeneration program in planaria
- Trichothiodystrophy in a child with occult learning disorder
- Faculty Opinions recommendation of Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis.
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Integrative Analysis of the Metabolome and Transcriptome Reveals the Mechanism Underlying Differences in Skin Development Between the New Zealand Rabbit and the Rex Rabbit
- Assessment of Human Nuclear Factor Erythroid 2 Related Factor 2 (NRF2) in Androgenetic Alopecia in Egyptian Men
- Proteome Analysis of Human Hair Shaft