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Research 91–120 of 112
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- Molecular Basis of Hereditary Hair Diseases
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Faculty Opinions recommendation of Association of topical minoxidil with autosomal recessive woolly hair/hypotrichosis caused by LIPH pathogenic variants.
- Mouse Hair Cycle Expression Dynamics Modeled as Coupled Mesenchymal and Epithelial Oscillators
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Identification of N6-Methyladenosine-Related Factors and the Prediction of the Regulatory Mechanism of Hair Follicle Development in Rex and Hycole Rabbits
- Hair Follicle Signaling Networks: A Dermal Papilla–Centric Approach
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Astragalus membranaceus and Cinnamomum cassia Stimulate the Hair Follicle Differentiation-Related Growth Factor by the Wnt/β-Catenin Signaling Pathway
- Enanthem in Patients With COVID-19 and Skin Rash
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Claves diagnósticas en displasias pilosas II
- Minoxidil
- Adverse Reactions to Biologic Medications Used in Allergy and Immunology Diseases
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation