Variable Degrees of 1-α Hydroxylase Activity--Fine Tuning the Rachitic Rheostat
Novel Gene Mutations in Patients with 1α-Hydroxylase Deficiency That Confer Partial Enzyme Activity in Vitro
Functional Genomics and Proteomics in Term and Preterm Parturition
Human Myometrial Genes Are Differentially Expressed in Labor: A Suppression Subtractive Hybridization Study
Primary Infertility in 45-Year-Old Man with Untreated 21-Hydroxylase Deficiency: Successful Outcome with Glucocorticoid Therapy
From the Editor-in-Chief
Genetic Causes of Human Reproductive Disease
The Genetics of Hereditary Nonmedullary Thyroid Carcinoma
Genetic Control of Susceptibility to Osteoporosis
Molecular Pathogenesis of Hypophosphatemic Rickets
Protein-Tyrosine Phosphatases: Emerging Targets for Therapeutic Intervention in Type 2 Diabetes and Related States of Insulin Resistance
Monogenic Disorders of Puberty
Pharmacogenomics in Endocrinology
An Unusual Phenotype of Frasier Syndrome due to IVS9 +4C>T Mutation in the WT1 Gene: Predominantly Male Ambiguous Genitalia and Absence of Gonadal Dysgenesis
Mutant Luteinizing Hormone Receptors in a Compound Heterozygous Patient with Complete Leydig Cell Hypoplasia: Abnormal Processing Causes Signaling Deficiency
Long-Term Progestin Treatment Inhibits RANTES (Regulated on Activation, Normal T Cell Expressed and Secreted) Gene Expression in Human Endometrial Stromal Cells
Human Resistin Gene: Molecular Scanning and Evaluation of Association with Insulin Sensitivity and Type 2 Diabetes in Caucasians
ONYX-015, an E1B Gene-Defective Adenovirus, Induces Cell Death in Human Anaplastic Thyroid Carcinoma Cell Lines
Nine Novel Mutations in Maturity-Onset Diabetes of the Young (MODY) Candidate Genes in 22 Spanish Families
Overexpression of Aromatase P450 in Leiomyoma Tissue Is Driven Primarily through Promoter I.4 of the Aromatase P450 Gene (CYP19)
Germline Mutations of TSH Receptor Gene as Cause of Nonautoimmune Subclinical Hypothyroidism
A Novel Nonstop Mutation in the Stop Codon and a Novel Missense Mutation in the Type II 3β-Hydroxysteroid Dehydrogenase (3β-HSD) Gene Causing, Respectively, Nonclassic and Classic 3β-HSD Deficiency Congenital Adrenal Hyperplasia
A Polymorphism within the Vitamin D-Binding Protein Gene Is Associated with Graves’ Disease but Not with Hashimoto’s Thyroiditis
AIRE Mutations and Human Leukocyte Antigen Genotypes as Determinants of the Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Phenotype
Expression and Function of Vasoactive Intestinal Peptide, Pituitary Adenylate Cyclase-Activating Polypeptide, and Their Receptors in the Human Adrenal Gland
STADY III: International Symposium on Signal Transduction in Health and Disease Tel Aviv, Israel October 1-4, 2002
Regulated Expression of Signal Transducer and Activator of Transcription, Stat5, and its Enhancement of PRL Expression in Human Endometrial Stromal Cells in Vitro
Identification of Three Novel Mutations in the KAL1 Gene in Patients with Kallmann Syndrome
Remission of Graves’ Hyperthyroidism and A/G Polymorphism at Position 49 in Exon 1 of Cytotoxic T Lymphocyte-Associated Molecule-4 Gene
Relation between Disease Phenotype and HLA-DQ Genotype in Diabetic Patients Diagnosed in Early Adulthood
First International Symposium on Insulin Action, Insulin Resistance, Inflammation, and Atherosclerosis Niagara Falls, New York September 20-22, 2002
Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome
Newly Proposed Hormonal Criteria via Genotypic Proof for Type II 3β-Hydroxysteroid Dehydrogenase Deficiency
An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity
Massachusetts General Hospital Reproductive Endocrine Unit
Phospholipase A2 and Cyclooxygenase Gene Expression in Human Preimplantation Embryos
Expression of Phosphorylated p27Kip1 Protein and Jun Activation Domain-Binding Protein 1 in Human Pituitary Tumors
Localization of the Activin Signal Transduction Components in Normal Human Ovarian Follicles: Implications for Autocrine and Paracrine Signaling in the Ovary
A Novel, C-Terminal Dominant Negative Mutation of the GR Causes Familial Glucocorticoid Resistance through Abnormal Interactions with p160 Steroid Receptor Coactivators
Genetic Analysis of Japanese Patients with 21-Hydroxylase Deficiency: Identification of a Patient with a New Mutation of a Homozygous Deletion of Adenine at Codon 246 and Patients without Demonstrable Mutations within the Structural Gene for CYP21
HOXA11 Silencing and Endogenous HOXA11 Antisense Ribonucleic Acid in the Uterine Endometrium
A Family of Autosomal Dominant Hypocalcemia with a Positive Correlation between Serum Calcium and Magnesium: Identification of a Novel Gain of Function Mutation (Ser820Phe) in the Calcium-Sensing Receptor
Fifth International Congress International Society for Neuroimmunomodulation
Frequent Occurrence of an Intron 4 Mutation in Multiple Endocrine Neoplasia Type 1
Two Novel Aquaporin-2 Mutations Responsible for Congenital Nephrogenic Diabetes Insipidus in Chinese Families
Expression of the mRNA Coding for 11β-Hydroxysteroid Dehydrogenase Type 1 in Adipose Tissue from Obese Patients: An in Situ Hybridization Study
ERβ1 and the ERβ2 Splice Variant (ERβcx/β2) Are Expressed in Distinct Cell Populations in the Adult Human Testis
Gender-Specific Responses of Lean Body Composition and Non-Gender-Specific Cardiac Function Improvement after GH Replacement in GH-Deficient Adults
Longitudinal Study of Serum Placental GH in 455 Normal Pregnancies: Correlation to Gestational Age, Fetal Gender, and Weight
GHRH Plus Arginine in the Diagnosis of Acquired GH Deficiency of Childhood-Onset
Glucocorticoid Replacement in Pituitary Surgery: Guidelines for Perioperative Assessment and Management
GH Treatment in Adults with Chronic Liver Disease: A Randomized, Double-Blind, Placebo-Controlled, Cross-Over Study
Effects of 12 Months of GH Treatment on Cortical and Trabecular Bone Content of IGFs and OPG in Adults with Acquired GH Deficiency: A Double-Blind, Randomized, Placebo-Controlled Study
Decreased Plasma Adiponectin Concentrations in Women with Dyslipidemia
Androgens and Bone Density in Women with Hypopituitarism
Second International Symposium on Progestins, Progesterone Receptor Modulators and Progesterone Antagonists
Bone Density and Amenorrhea in Ballet Dancers Are Related to a Decreased Resting Metabolic Rate and Lower Leptin Levels
Effect of Pioglitazone on Abdominal Fat Distribution and Insulin Sensitivity in Type 2 Diabetic Patients
Alendronate Increases Bone Mass and Reduces Bone Markers in Postmenopausal African-American Women
Marked Disproportionality in Bone Size and Mineral, and Distinct Abnormalities in Bone Markers and Calcitropic Hormones in Adult Turner Syndrome: A Cross-Sectional Study
Fifth Annual Scientific ForumSoutheast Lipid Association
Recurrent Iodine Deficiency in Tasmania, Australia: A Salutary Lesson in Sustainable Iodine Prophylaxis and Its Monitoring
The in Vivo Control of Prostaglandin H Synthase-2 Messenger Ribonucleic Acid Expression in the Human Amnion at Parturition
Novel Mutations in CYP21 Detected in Individuals with Hyperandrogenism
Trialkyltin Compounds Enhance Human CG Secretion and Aromatase Activity in Human Placental Choriocarcinoma Cells
Short-Term Effects of Glucocorticoids in the Human Fetal-Placental Circulation in Vitro
Second Transplant Bone Disease Meeting (TBDM 2002)
Modulation of Endometrial Redox Balance during the Menstrual Cycle: Relation with Sex Hormones
Growth Differentiation Factor-9 Inhibits 3′5′-Adenosine Monophosphate-Stimulated Steroidogenesis in Human Granulosa and Theca Cells
Pituitary Function in a Man with Congenital Aromatase Deficiency: Effect of Different Doses of Transdermal E2 on Basal and Stimulated Pituitary Hormones
Increased Orderliness of Growth Hormone (GH) Secretion in GH-Deficient Adults with Low Serum Insulin-Like Growth Factor I
Ninth International Congress on Obesity
Additive Effects of Insulin-Sensitizing and Anti-Androgen Treatment in Young, Nonobese Women with Hyperinsulinism, Hyperandrogenism, Dyslipidemia, and Anovulation
Placental GH, IGF-I, IGF-Binding Protein-1, and Leptin during a Glucose Challenge Test in Pregnant Women: Relation with Maternal Body Weight, Glucose Tolerance, and Birth Weight
Effects of Recombinant Human IGF-I and Oral Contraceptive Administration on Bone Density in Anorexia Nervosa
Evidence that the IL-6/IL-6 Soluble Receptor Cytokine System Plays a Role in the Increased Skeletal Sensitivity to PTH in Estrogen-Deficient Women
Comparison of Insulin Sensitivity, Clearance, and Secretion Estimates Using Euglycemic and Hyperglycemic Clamps in Children
QUICKI Is Useful for Following Improvements in Insulin Sensitivity after Therapy in Patients with Type 2 Diabetes Mellitus
Leptin Gene Polymorphism Is Associated with Hypertension Independent of Obesity
FFA-Induced Endothelial Dysfunction Can Be Corrected by Vitamin C
Hyperglycemic Clamp Assessment of Insulin Secretory Responses in Normal Subjects Treated with Olanzapine, Risperidone, or Placebo
Progesterone Withdrawal and Estrogen Activation in Human Parturition Are Coordinated by Progesterone Receptor A Expression in the Myometrium
Quantification of the Soluble Leptin Receptor in Human Blood by Ligand-Mediated Immunofunctional Assay
Vitamin E Supplementation Reduces Plasma Vascular Cell Adhesion Molecule-1 and von Willebrand Factor Levels and Increases Nitric Oxide Concentrations in Hypercholesterolemic Patients
Close Juxtapositions between LHRH Immunoreactive Neurons and Substance P Immunoreactive Axons in the Human Diencephalon
Uterine Glands Provide Histiotrophic Nutrition for the Human Fetus during the First Trimester of Pregnancy
Steroid Receptor Coactivator Expression throughout the Menstrual Cycle in Normal and Abnormal Endometrium
25-Hydroxyvitamin D3-1α-Hydroxylase Expression in Normal and Pathological Parathyroid Glands
Novel Homozygous Splice Acceptor Site GnRH Receptor (GnRHR) Mutation: Human GnRHR “Knockout”
Free and Total Insulin-Like Growth Factor (IGF)-I Levels Decline during Fasting: Relationships with Insulin and IGF-Binding Protein-1
Expression of Multiple Corticotropin–Releasing Hormone Receptors in the Human Heart
Authors' Response: Expression of Multiple Corticotropin–Releasing Hormone Receptors in the Human Heart
Serum Cortisol and 7–Hydroxyprogsterone Concentrations in Children with Classic Congenital Adrenal Hyperplasia
Author's Response: Serum Cortisol and 17–Hydroxyprogesterone Concetrations in Children with Classic Congenital Adrenal Hyperplasia
TSH Receptor Expression in Cardiac Muscle Tissue
Occurrence of Pheochromocytoma in a MEN2A family with Codon 605 Mutation of the RET Protooncogene
Endocrine-Related Resources from the National Institutes of Health