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Research 241–270 of 1000+
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Evolution of Trichocyte Keratins
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Methyl Jasmonate Activates the 2C Methyl-D-erithrytol 2,4-cyclodiphosphate Synthase Gene and Stimulates Tanshinone Accumulation in Salvia miltiorrhiza Solid Callus Cultures
- Regulatory network of ginsenoside biosynthesis under Ro stress in the hairy roots of Panax ginseng revealed by RNA sequencing
- Molecular landscape of lung cancer: insights into therapeutic targets and clinical outcomes
- Hair Follicle Transcriptome Analysis Reveals Differentially Expressed Genes That Regulate Wool Fiber Diameter in Angora Rabbits
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Expression profile of long non-coding RNA in inner Mongolian cashmere goat with putative roles in hair follicles development
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Transcriptomes reveal microRNAs and mRNAs in different photoperiods influencing cashmere growth in goat
- Industry updates in advanced therapy medicinal products and regenerative medicine – March 2026
- Genetic Polymorphisms of the 3'-Untranslated Regions (3'-UTR) of the HSP 70 Gene in Moa Buffalo (Bubalus bubalis)
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- 821 Pigmentation and autophagy in alopecia areata pathogenesis
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Dermatologic Manifestations of Polycystic Ovary Syndrome
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Dynamic changes of genomic methylation profiles at different growth stages in Chinese Tan sheep
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Genetic Hair Disorders: A Review