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Research 541–570 of 1000+
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Ulcerative colitis and total alopecia in a mother and her son
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- The association between HDAC9 gene polymorphisms and stroke risk in the Chinese population: A meta-analysis
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Sacituzumab Govitecan-Hziy (Trodelvy™)
- Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Finding bald spots on chromosome 20p11
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Association of Androgen Receptor CAG Repeat Length with Polycystic Ovary Syndrome in an Iranian Female Population
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Genetic and Environmental Factors Affecting Hair Density in East Asian Populations
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Effects of <i>KISS1</i> structural polymorphism on the risk of polycystic ovary syndrome and reproductive hormones in Iraqi women who take metformin
- 177 The Striatin-Interacting Phosphatase And Kinases complex is important for skin epidermal differentiation and barrier formation
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease