Search
for
Sort by
Research 61–90 of 1000+
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Berardinelli–Seip syndrome
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Hair Protein Polymorphism and Its Application to Forensic Science Hair Comparison.
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Keratins: the hair shaft's backbone revealed
- Pallister-Killian Syndrome
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- A Short Report on Melanocyte/Melanoma Culture, Senescence, and Reproducibility
- Pathophysiology, conventional treatments, and evidence-based herbal remedies of hair loss with a systematic review of controlled clinical trials
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.
- The Clinical Presentation of Systemic Lupus Erythematosus
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Research progress on the pathogenesis of androgenetic alopecia
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Alopecia androgenética: aspectos etiopatogênicos, métodos diagnósticos e condutas terapêuticas
- Human hair keratins
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia
- Electrophoretic analysis of human hair keratins
- Understanding host-graft crosstalk for predicting the outcome of stem cell transplantation
- Framing the Problem: The Mystery of Post-Finasteride Syndrome and Reasons to Suspect a Microbial Factor
- Fertility and Sterility Vol 101 No 4, April 2014
- 線維芽細胞凝集塊形成による幹細胞形成機構の解明