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Research 31–60 of 89
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Genetics of Alopecia
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- 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
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- The bright side of fibroblasts: molecular signature and regenerative cues in major organs
- Hair Loss in Children
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Hair Dermal papilla maintain its hair inducing characteristics via autocrine exosomal miR-23a-3p
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- TNC+ fibroblasts involve in skin inflammation via neuro-immune and interacting with T cells
- LncRNAs regulate the cyclic growth and development of hair follicles in Dorper sheep
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Alopezien und Hypotrichosen im Kindesalter
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Lysophosphatidic acid and signaling in sensory neurons
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations