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Research 841–870 of 1000+
- 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
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- 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
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase 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
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- 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
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease
- 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
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
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- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Efficacy and safety of SGLT2 inhibitor on insulin resistance and hyperglycemia in Werner syndrome—A case report