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Research 211–240 of 1000+
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Androgenetic Alopecia in Men: An Update On Genetics
- Congenital Adrenal Hyperplasia
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Epidemiology and burden of alopecia areata: a systematic review
- Clinical biochemistry of dihydrotestosterone
- Novel circRNAs from cashmere goats: Discovery, integrated regulatory network, and their putative roles in the regeneration and growth of secondary hair follicles
- miR-129-5p Participates in Hair Follicle Growth by Targeting HOXC13 in Rabbit
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Predominant expression of 5 alpha-reductase type 1 in pubic skin from normal subjects and hirsute patients.
- Congenital Adrenal Hyperplasia
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Thymosin β4 Promotes Dermal Healing
- Hétérogénéité tumorale du cancer de la prostate et infection par le SARS-CoV2 : une relation complexe impliquant les vésicules extracellulaires et le récepteur des androgènes
- Poster Abstracts
- GSDMA deficiency impairs cutaneous squamous cell carcinoma growth
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Allelic frequencies for the seventeen Y-STR loci observed in Iraqi male patients with prostate cancer
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Polycystic Ovary Syndrome in Adolescents
- SWEET SYNDROME: AN UNUSUAL PRESENTATION OF CHRONIC GRANULOMATOUS DISEASE IN A CHILD