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Research 571–600 of 1000+
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- A mutation in MAP2 is associated with prenatal hair follicle density
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Diabetes Mellitus and Prostate Cancer Risk—A Systematic Review and Meta-Analysis
- Role of sgk1 in cancer: a bibliometric analysis from 2013 to 2023—review article
- Quantitative morphometric analysis of hair follicles in alopecia areata
- Global trends in tertiary lymphoid structures: a bibliometric analysis from 2014 to 2023
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Mendelian randomization analysis of the causal relationship between low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and androgenic alopecia
- Multi-omics analysis unveils the role of cancer-associated fibroblasts in cutaneous squamous cell carcinoma
- Whole-transcriptome analysis reveals the profiles and roles of coding and non-coding RNAs during hair follicle cycling in Rex rabbits
- Comprehensive Administrative and Engineering Strategies for Radiation Protection and Occupational Health Safety
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Vitamin D deficiency in non-scarring and scarring alopecias: a systematic review and meta-analysis
- LB1034 Meta-analysis of scalp transcriptome defines alopecia areata subtypes and molecular response to four (4) treatments with jak inhibiting properties
- RETRACTED: The impact of different antibiotic injection regimens on patients with severe infections: A meta‐analysis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis