Endocrine Reviews

Endocr Rev · ISSN (print) 0163-769X · ISSN (e) 1945-7189 · 32 papers in corpus
review 2009
doi:10.1210/er.2008-0021 ·PMID:19074586

In 1991, a group of 21 scientists gathered at the Wingspread Conference Center to discuss evidence of developmental alterations observed in wildlife populations after chemical exposures. There, the term "endocrine disruptor" was agreed upon…

guideline 2009
doi:10.1210/er.2009-0002 ·PMID:19502515

There is growing interest in the possible health threat posed by endocrine-disrupting chemicals (EDCs), which are substances in our environment, food, and consumer products that interfere with hormone biosynthesis, metabolism, or action res…

review 2009
doi:10.1210/er.2009-0005 ·PMID:19770291

Kisspeptin (a product of the Kiss1 gene) and its receptor (GPR54 or Kiss1r) have emerged as key players in the regulation of reproduction. Mutations in humans or genetically targeted deletions in mice of either Kiss1 or Kiss1r cause profoun…

review 2009
doi:10.1210/er.2009-0012 ·PMID:19776209

Two major functions of the mammalian ovary are the production of germ cells (oocytes), which allow continuation of the species, and the generation of bioactive molecules, primarily steroids (mainly estrogens and progestins) and peptide grow…

review 2005
doi:10.1210/er.2004-0021 ·PMID:16160098

In women, endometrial morphology and function undergo characteristic changes every menstrual cycle. These changes are crucial for perpetuation of the species and are orchestrated to prepare the endometrium for implantation of a conceptus. I…

review 2005
doi:10.1210/er.2005-0001 ·PMID:15857972

Selective progesterone receptor modulators (SPRMs) represent a new class of progesterone receptor ligands. SPRMs exert clinically relevant tissue-selective progesterone agonist, antagonist, or mixed agonist/antagonist effects on various pro…

review 1986
doi:10.1210/edrv-7-1-106 ·PMID:3007079

Agonist analogs of GnRH are being increasingly utilized to induce medical castration for treatment of a variety of hormonally responsive clinical disorders. However, the mechanism/s of their paradoxical antigonadal action in the human male …