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Research 91–120 of 1000+
- CRISPR–Cas9: A History of Its Discovery and Ethical Considerations of Its Use in Genome Editing
- Hair loss in women
- A woman with iatrogenic androgenetic alopecia responding to finasteride
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Molecular Genetics of Alopecias
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic, hormonal and metabolic aspects of PCOS: an update
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- What does acne genetics teach us about disease pathogenesis?
- Genetic basis of polycystic ovary syndrome
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Genetic Defects of Female Sexual Differentiation
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- 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
- Reversal of andro-genetic alopecia in a male. A spironolactone effect?
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Biology and Genetics of Hair
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Dermatopathology and molecular genetics
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- The hair shaft: normality, abnormality, and genetics
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention