Search
for
Sort by
Research 121–150 of 1000+
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Genetics of Alopecia
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Hypotrichosis in a child with olmsted syndrome
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- TRPV3 Ion Channel: From Gene to Pharmacology
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Dysfunction of keratinocyte adhesion
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Improving human forensics through advances in genetics, genomics and molecular biology
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- SUMMARIES OF PAPERS
- Inherited Epidermolysis Bullosa: A Clinical Case
- The Spectrum of Skin Disease Among Indian Children
- National scientific medical meeting 1996 abstracts
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Keratosis follicularis spinulosa decalvans in a female
- Comparative Anatomy of Mouse and Human Nail Units
- Analogs of human genetic skin disease in domesticated animals