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Research 571–600 of 1000+
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Regenerative Medicine of Epidermal Structures
- The zinc finger protein 3 of Arabidopsis thaliana regulates vegetative growth and root hair development
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Multi-Walled Carbon Nanotubes Can Promote Brassica napus L. and Arabidopsis thaliana L. Root Hair Development through Nitric Oxide and Ethylene Pathways
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Netherton Syndrome – Responding to Oral Retinoids
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Bachmann–Bupp syndrome and treatment
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- A Clinical Review of Trichorrhexis Nodosa
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”
- Transcriptomic analyses of regenerating adult feathers in chicken
- Congenital atrichia associated with situs inversus and mesocardia
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players