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Research 241–270 of 1000+
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- IMPACT OF BIOMARKER IN PREDICATIVE TO RESPONSE ADJUVANT CHEMOTHERAPY AND OVERALL SURVIVAL IN FEMALES INFECTED WITH BREAST CANCER: A REVIEW ARTICLES
- 1345 A single-cell RNA map of perinatal developing mouse skin
- 034 Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1
- Generalised Glucocorticoid Resistance
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Hair regrowth in a patient with central centrifugal cicatricial alopecia after a 2-month trial of baricitinib
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Impact of One-Week Administration of Dihydrotestosterone in Rat Anterior Pituitary Gland
- An Updated Nomenclature for Keratin-Associated Proteins (KAPs)
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Efficient Editing of CSLD2 Orthologue by CRISPR/Cas9 Affects Cell Morphogenesis of Root Hair in Spinach
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- 男性型脱毛症の原因についての手がかり
- Palatogenesis and cutaneous repair: A two‐headed coin
- 559 Induction of tissue-specific premature stem cell aging promotes senescence-like phenotypes in remote multiple organs
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Exploring the mechanism of stigmasterol against androgenetic alopecia using geometry optimization, network pharmacology, molecular docking, and molecular dynamics studies
- Bioinformatics analysis of EST segment from goat
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Congenital adrenal hyperplasia
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- 1363 Hair follicle growth and pigmentation during ageing
- The color of human hair
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review