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Research 631–660 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
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- 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
- Abstracts
- Ultraviolet Radiation in Wound Care: Sterilization and Stimulation
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Wnt signaling: the good and the bad
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- 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
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Defining the identity of mouse embryonic dermal fibroblasts
- 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
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series