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Research 61–90 of 120
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Alopezien und Hypotrichosen im Kindesalter
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Recent advances in the epidermal growth factor receptor/ligand system biology on skin homeostasis and keratinocyte stem cell regulation
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Dermatoscopy of hair shaft disorders
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- Intelligent nanotherapeutic strategies for the delivery of CRISPR system
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Hair Follicle Signaling Networks: A Dermal Papilla–Centric Approach
- Genetic Hair Disorders: A Review
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics