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Research 31–60 of 1000+
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Androgenetic Alopecia in Men: An Update On Genetics
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Androgen receptors and their biology
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Molecular basis of androgen insensitivity
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- 921 Generation of a new rodent model of scleroderma
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Function of KLF4 in Stem Cell Biology
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- The Paradox of p53: What, How, and Why?
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A missing piece: the spiny mouse and the puzzle of menstruating species
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene