• 17β-Estradiol is critical for the preovulatory induction of prostaglandin E(2) synthesis in mice
• 46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters
• 46,XX Differences of Sex Development outside congenital adrenal hyperplasia: pathogenesis, clinical aspects, puberty, sex hormone replacement therapy and fertility outcomes
• 46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features
• A case of Aromatase deficiency due to a novel CYP19A1 mutation
• A large cohort of disorders of sex development and their genetic characteristics: 6 novel mutations in known genes
• A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue
• A Novel Homozygous <em>CYP19A1</em> Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation
• A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase Deficiency
• A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation
• A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans
• Abnormal steroidogenesis and aromatase activity in preeclampsia
• Accelerated Pubertal Tempo in a 46,XY Aromatase-Deficient Patient
• Altered umbilical sex steroids in preterm infants born small for gestational age
• Amh/Amhr2 Signaling Causes Masculinization by Inhibiting Estrogen Synthesis during Gonadal Sex Differentiation in Japanese Flounder (<em>Paralichthys olivaceus</em>)
• An aroma of complexity: how the unique genetics of aromatase (CYP19A1) explain diverse phenotypes from hens and hyenas to human gynecomastia, and testicular and other tumors
• An Intron 9 CYP19 Gene Variant (IVS9+5G&gt;A), Present in an Aromatase-Deficient Girl, Affects Normal Splicing and Is Also Present in Normal Human Steroidogenic Tissues
• Analysis of the effect of estrogen/androgen perturbation on penile development in transgenic and diethylstilbestrol-treated mice
• Aromatase and estrogen receptor α deficiency
• Aromatase deficiency caused by mutation of <em>CYP19A1</em> gene: A case report
• Aromatase deficiency caused by mutation of CYP19A1 gene: A case report
• Aromatase Deficiency due to a Homozygous CYP19A1 Mutation in a 46,XX Egyptian Patient with Ambiguous Genitalia
• Aromatase Deficiency due to a Novel Mutation in <em>CYP19A1</em> Gene
• Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene
• Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism
• Aromatase deficiency in a male patient - Case report and review of the literature
• Aromatase deficiency in a tall man: Case report of two novel mutations and review of literature
• Aromatase deficiency in an adolescent girl misdiagnosed as congenital adrenal hyperplasia in infancy and childhood
• Aromatase deficiency in an Ontario Old Order Mennonite family
• Aromatase deficiency in hematopoietic cells improves glucose tolerance in male mice through skeletal muscle-specific effects
• Aromatase deficiency in transplanted bone marrow cells improves vertebral trabecular bone quantity, connectivity, and mineralization and decreases cortical porosity in murine bone marrow transplant recipients
• Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the <em>CYP19A1</em> Gene
• Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene
• Aromatase deficiency, a rare syndrome: case report
• Aromatase deficiency: A case series of 46, XX Chinese children and a systematic review of the literature
• Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization
• Aromatase deficiency: a rare cause of maternal virilisation and ambiguous genitalia in neonates
• Aromatase deficiency: an unusual cause for primary amenorrhea with virilization
• Aromatase deficiency: rare cause of virilization
• Aromatase excess syndrome: a rare autosomal dominant disorder leading to pre- or peri-pubertal onset gynecomastia
• Aromatase is required for female abdominal aortic aneurysm protection
• Aromatase mutation in men as a rare cause of osteoporosis: a case report and review of the literature
• Aromatase-Inhibitor-Induced Musculoskeletal Inflammation Is Observed Independent of Oophorectomy in a Novel Mouse Model
• Aromatase-null mice expressing enhanced green fluorescent protein in germ cells provide a model system to assess estrogen-dependent ovulatory responses
• Association of the <em>CYP19A1</em> rs700518 Polymorphism with Selected Markers of Bone Metabolism in Women with Hyperandrogenism
• Case Report: Anastrozole as a monotherapy for pre-pubertal children with non-classic congenital adrenal hyperplasia
• Characterisation of a Mouse Model of Breast Cancer with Metabolic Syndrome
• Characterization of a novel CYP19A1 (aromatase) R192H mutation causing virilization of a 46,XX newborn, undervirilization of the 46,XY brother, but no virilization of the mother during pregnancies
• Child with '46, XX' disorder of sex development: clues to diagnose aromatase deficiency
• Comparison of Placental HSD17B1 Expression and Its Regulation in Various Mammalian Species
• Congenital disorders of estrogen biosynthesis and action
• Development and Characterization of Inducible Astrocyte-Specific Aromatase Knockout Mice
• Diagnosis and management of non-CAH 46,XX disorders/differences in sex development
• Differential effects of variations in human P450 oxidoreductase on the aromatase activity of CYP19A1 polymorphisms R264C and R264H
• Endometriosis and adenomyosis: shared pathophysiology
• Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis
• Exposure to tris(2,6-dimethylphenyl) phosphate interferes with sexual differentiation via estrogen receptors 2a and 2b in zebrafish
• Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial
• Fertility issues in the management of patients with disorders of sex development
• Five new cases of 46,XX aromatase deficiency: clinical follow-up from birth to puberty, a novel mutation, and a founder effect
• Genomic basis of aromatase excess syndrome: recombination- and replication-mediated rearrangements leading to CYP19A1 overexpression
• Gestational Hyperandrogenism in Developmental Programming
• Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency
• Gulp1 deficiency augments bone mass in male mice by affecting osteoclasts due to elevated 17β-estradiol levels
• Hepatic glucose intolerance precedes hepatic steatosis in the male aromatase knockout (ArKO) mouse
• Higher Insulin Resistance and Adiposity in Postmenopausal Women With Breast Cancer Treated With Aromatase Inhibitors
• Hypothesis: Persistently elevated hCG causes gestational ovarian overstimulation associated with prolonged postpartum hyperandrogenism in mothers of aromatase-deficient babies
• Impact of aromatase absence on murine intraocular pressure and retinal ganglion cells
• Impact of estrogen replacement throughout childhood on growth, pituitary-gonadal axis and bone in a 46,XX patient with CYP19A1 deficiency
• Influence of aromatase absence on the gene expression and histology of the mouse meibomian gland
• Kennedy's disease: clinical significance of tandem repeats in the androgen receptor
• Leflutrozole in Male Obesity-Associated Hypogonadotropic Hypogonadism: Ph 2b Double-Blind Randomised Controlled Trial
• Longitudinal multi-omics study of palbociclib resistance in HR-positive/HER2-negative metastatic breast cancer
• Macroorchidism in childhood and adolescence: an update
• Managing Bone Health in Breast Cancer
• Maternal exposure to imazalil disrupts the endocrine system in F₁ generation mice
• Metabolic and Blood Pressure Effects of Walnut Supplementation in a Mouse Model of the Metabolic Syndrome
• Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype
• Molecular diagnostics of disorders of sexual development: an Indian survey and systems biology perspective
• Myocardial and cardiomyocyte stress resilience is enhanced in aromatase-deficient female mouse hearts through CaMKIIδ activation
• Novel <em>CYP19A1</em> Mutations Extend the Genotype-Phenotype Correlation and Reveal the Impact on Ovarian Function
• Of Oestrogens and Sperm: A Review of the Roles of Oestrogens and Oestrogen Receptors in Male Reproduction
• Ovarian and uterine development and hormonal feedback mechanism in a 46 XX patient with CYP19A1 deficiency under low dose estrogen replacement
• Ovarian cysts in prepubertal girls
• PARP2 promotes inflammation in psoriasis by modulating estradiol biosynthesis in keratinocytes
• Placental Aromatase Is Deficient in Placental Ischemia and Preeclampsia
• Postnatal aromatase blockade increases c-fos mRNA responses to acute restraint stress in adult male rats
• Progress on growth promoting therapies other than growth hormone
• Reversibility in male idiopathic osteoporosis possible
• RNA-seq and LC-MS/MS analysis of antiviral effects mediated by cold stress and stress hormone corticosterone in chicken DF-1 cells
• Role of aromatase in sex-specific cerebrovascular endothelial function in mice
• Role of sex steroids hormones in the regulation of bone metabolism in men: Evidence from clinical studies
• Sex steroids and bone health status in men
• Sexual dimorphism in the glucose homeostasis phenotype of the Aromatase Knockout (ArKO) mice
• The BET inhibitor/degrader ARV-825 prolongs the growth arrest response to Fulvestrant + Palbociclib and suppresses proliferative recovery in ER-positive breast cancer
• THE EFFECTS OF MATERNAL HYPOTHYROIDISM ON THE IMMUNOREACTIVITY OF CYTOCHROME P450 AROMATASE IN THE POSTNATAL RAT TESTICLES
• The two kisspeptin neuronal populations are differentially organized and activated by estradiol in mice
• The Update of Obesity Syndrome: Molecular Mechanism, Pathophysiology and Therapies. Topics: I. Recent Topics on Diagnosis and Pathophysiology of the Obesity Syndrome: 1. Obesity secondary to endocrinological disorders
• Virilization of a 46,XX Fetus Following Aromatase Inhibitor Treatment of Breast Cancer
• Vitamin D during treatment for breast cancer - the perspective of active self-help group leaders