Search
for
Sort by
Research 241–270 of 1000+
- Case of non-Herlitz junctional epidermolysis bullosa with<i>COL17A1</i>mutation
- ТУБЕРОЗНЫЙ СКЛЕРОЗ (БУРНЕВИЛЛЯ-ПРИНГЛА). ОБЗОР ЛИТЕРАТУРЫ
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Diffuse hypotrichosis from early childhood
- Five SNP variability in male pattern hair loss patients and healthy individuals from Russia
- Przewidywanie cech wyglądu człowieka na podstawie markerów DNA do celów medyczno-sądowych i kryminalistycznych
- Frontal fibrosing alopecia: reflections and hypotheses on aetiology and pathogenesis
- Skin Keratins
- Patent Reports
- Core Curriculum for Hair Restoration Surgery, Recommended by the International Society of Hair Restoration Surgery (ISHRS)
- THE PATHOGENESIS OF ALOPECIA AREATA
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- PCOS: update and diagnostic approach
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Insight into the pathogensis of polycystic ovarian syndrome
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Dermatomyositis Disease in Dogs
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Netherton Syndrome
- Male androgenetic alopecia
- Double-Lined Frontoparietal Scleroderma en coup de sabre
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- 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
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Early Exposure to Sexualized Content and Androgenetic Alopecia: Can Culture Shape Our Biology?
- Clinical cases of Darier-White follicular dyskeratosis