Search
for
Sort by
Research 301–330 of 1000+
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Alopecia in a 19-Month-Old Boy