Search
for
Sort by
Research 151–180 of 1000+
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- The Rotterdam Study: 2016 objectives and design update
- Skin aging: mechanisms, evaluation, and rejuvenation
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Roles for Msx and Dlx homeoproteins in vertebrate development
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Targeted expression of SV40 T antigen in the hair follicle of transgenic mice produces an aberrant hair phenotype
- Dermal papilla cells and melanocytes response to physiological oxygen levels depends on their interactions
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Epigenetic age estimation in saliva and in buccal cells
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Molecular basis of androgen insensitivity
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Drug Repurposing for Rare Diseases
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Elevated <em>DKK1</em> expression is an independent unfavorable prognostic indicator of survival in head and neck squamous cell carcinoma
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Weathering the Storm: Harnessing the Resolution of Inflammation to Limit COVID-19 Pathogenesis
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Factors regulating quiescent stem cells: insights from the intestine and other self-renewing tissues
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis