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Research 931–960 of 1000+
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- A kindred with mutant IKAROS and autoimmunity
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Participation of CD34-enriched mouse adipose cells in hair morphogenesis
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Skin morphology of the mutant hairless USP mouse
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Establishment of Tsc2-deficient rat embryonic stem cells
- Congenital atrichia with papular lesions
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Episodic Bilateral Corneal Edema Caused by Hair Groom Gel
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Growing Up Fast: Managing Autism Spectrum Disorder and Precocious Puberty
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review