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Research 301–330 of 1000+
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Sex-Related Differences in the Pharmacological Response in SARS-CoV-2 Infection, Dyslipidemia, and Diabetes Mellitus: A Narrative Review
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- 66-Year-Old Woman With Painless Vesicular Lesions
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- A Scoping Review of Pharmacotherapy, Complementary, and Alternative Medicine (CAM), and Surgical Therapies for Androgenic Alopecia
- Increased PHGDH expression promotes aberrant melanin accumulation
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- Male pattern hair loss: Taking one for the team: The selfless gene
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- 196 The endocannabinoid tone regulates human sebocyte biology
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Why Some Women Look Young for Their Age
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Gender aspects in skin diseases
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Skin manifestations among<i>GATA2</i>-deficient patients
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Primary Scarring Alopecia: Clinical-Pathological Review of 72 Cases and Review of the Literature
- Concomitant presentation of alopecia areata in siblings: A rare occurrence
- Factors Driving Unique Urination Phenotypes of Male and Female 9-week-old C57BL/6J Mice