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Research 571–600 of 1000+
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Function of KLF4 in Stem Cell Biology
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Abstracts
- Wnt signaling: the good and the bad
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Defining the identity of mouse embryonic dermal fibroblasts
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in the<i>Arabidopsis</i>Root
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency