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Research 751–780 of 1000+
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Barbering in Laboratory Rodents: Problems and Prospects
- Diffuse loss of hair with papules
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Congenital Atrichia: A Case Report
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- LO-010 Relationship between the EULAR/ACR classification criteria and organ damage in systemic lupus erythematosus
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- AN SYNOPTIC OVERVIEW ON AUTOIMMUNE DISORDERS AND ITS MANAGEMENT
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Dermal EZH2 simultaneously orchestrates dermal differentiation and epidermal proliferation during murine skin development
- 574 Murine sebaceous gland homeostasis requires intact cutaneous innervation in a hair cycle-dependent context
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 573 Hair follicles employ a 2-dimensional healing strategy to repair 3-dimensional injuries
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Two females with hair loss
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- 公表学術論文等リスト 2018
- WNT10B (wingless-type MMTV integration site family)
- Mixing the Old with the New: Drug Repurposing for Immune Deficiency in the Era of Precision Medicine and Pediatric Genomics
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators