What is she best known for?
The fields of study she is best known for:
Receptor, Internal medicine, Endocrinology, Thyrotropin receptor and Biochemistry are her primary areas of study.
Sabine Costagliola interconnects Gonadotropin and Cell biology in the investigation of issues within Receptor.
Her Internal medicine study incorporates themes from Ovarian hyperstimulation syndrome and Pregnancy.
Her work on Human chorionic gonadotropin as part of general Endocrinology study is frequently connected to Membrane transport protein, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
In her work, Somatic cell and Point mutation is strongly intertwined with Transmembrane domain, which is a subfield of Thyrotropin receptor.
Her research integrates issues of Graves' disease, Chinese hamster ovary cell and Recombinant DNA in her study of Antibody.
Her most cited work include:
- Cloning of two human thyroid cDNAs encoding new members of the NADPH oxidase family. (524 citations)
- A molecular dissection of the glycoprotein hormone receptors. (288 citations)
- Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic Gonadotropin (263 citations)
What are the main themes of her work throughout her whole career to date?
Her main research concerns Endocrinology, Internal medicine, Receptor, Thyroid and Thyrotropin receptor.
Her Endocrinology research incorporates elements of Antibody and PAX8.
Her work focuses on many connections between Internal medicine and other disciplines, such as Mutation, that overlap with her field of interest in Transmembrane domain.
As part of her studies on Receptor, Sabine Costagliola often connects relevant areas like Molecular biology.
Her research in Thyroid intersects with topics in Embryonic stem cell, Zebrafish and Cell biology.
Her Thyrotropin receptor research includes elements of Agonist, Extracellular and Recombinant DNA.
She most often published in these fields:
- Endocrinology (44.69%)
- Internal medicine (44.69%)
- Receptor (35.75%)
What were the highlights of her more recent work (between 2011-2021)?
- Thyroid (24.58%)
- Cell biology (17.32%)
- Zebrafish (7.82%)
In recent papers she was focusing on the following fields of study:
Sabine Costagliola focuses on Thyroid, Cell biology, Zebrafish, Internal medicine and Hormone.
Her Thyroid research integrates issues from Embryonic stem cell, Morphogenesis and Neuroscience.
The various areas that Sabine Costagliola examines in her Cell biology study include Endoderm and Embryogenesis.
The study incorporates disciplines such as Phenotype, Signal transduction, Thyroid dysgenesis and Candidate gene in addition to Zebrafish.
The Phenotype study combines topics in areas such as NADPH oxidase, Mutant, Allele and ASPM.
Her Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and PAX8.
Between 2011 and 2021, her most popular works were:
- Generation of functional thyroid from embryonic stem cells. (206 citations)
- Transgenic zebrafish illuminate the dynamics of thyroid morphogenesis and its relationship to cardiovascular development. (47 citations)
- AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency (31 citations)
In her most recent research, the most cited papers focused on:
Sabine Costagliola spends much of her time researching Thyroid, Internal medicine, Endocrinology, Zebrafish and Mutation.
Her studies in Internal medicine integrate themes in fields like Cell biology, Gene and PAX8.
Her Endocrinology research is multidisciplinary, relying on both Amenorrhea and Folliculogenesis.
Her Zebrafish research includes themes of Congenital hypothyroidism, Thyroid dysgenesis, Morphogenesis, Organogenesis and Candidate gene.
The concepts of her Mutation study are interwoven with issues in Phenotype, Thyroid function, Computational biology and CRISPR.
Sabine Costagliola has researched Hormone in several fields, including Progenitor cell, Stem cell, Missense mutation and Cellular differentiation.
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