Search
for
Sort by
Research 781–810 of 1000+
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Scoping Review on the Use of Drugs Targeting JAK/STAT Pathway in Atopic Dermatitis, Vitiligo, and Alopecia Areata
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Early Onset Werner Syndrome
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Netherton Syndrome – Responding to Oral Retinoids
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy
- Werner's syndrome: incidental finding during pregnancy
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Converging physiological roles of the anthrax toxin receptors
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Congenital atrichia associated with situs inversus and mesocardia
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration