Papari-Zareei M.
55
Coauthors
10
Documentos
Volumen de publicaciones por año
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| Año de publicación | Num. Publicaciones |
|---|---|
| 2006 | 3 |
| 2007 | 1 |
| 2009 | 2 |
| 2010 | 2 |
| 2011 | 1 |
| 2012 | 1 |
Publicaciones por áreas de conocimiento
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| Área de conocimiento | Num. Publicaciones |
|---|---|
| Bioquímica | 11 |
| Genética | 8 |
| Farmacología | 3 |
| Cáncer | 2 |
| Enzima | 1 |
Publicaciones por áreas temáticas
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| Área temática | Num. Publicaciones |
|---|---|
| Enfermedades | 7 |
| Fisiología humana | 6 |
| Farmacología y terapéutica | 3 |
| Ginecología, obstetricia, pediatría, geriatría | 3 |
| Bioquímica | 3 |
| Fisiología y materias afines | 1 |
Principales fuentes de datos
| Origen | Num. Publicaciones |
|---|---|
| Scopus | 10 |
| Google Scholar | 0 |
| RRAAE | 0 |
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Coautores destacados por número de publicaciones
| Coautor | Num. Publicaciones |
|---|---|
| Richard J. Auchus | 10 |
| Li R. | 2 |
| Sharifi N. | 2 |
| Brandmaier A. | 2 |
| Sherbet D.P. | 2 |
| Rambally S. | 2 |
| Evaul K. | 1 |
| Lin L. | 1 |
| Gore M.E. | 1 |
| Taylor N.F. | 1 |
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Top Keywords
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Publicaciones del autor
Arginine 276 controls the directional preference of AKR1C9 (rat liver 3α-hydroxysteroid dehydrogenase) in human embryonic kidney 293 cells
ArticleAbstract: Rat liver AKR1C9 is the best-studied 3α-hydroxysteroid dehydrogenase (3αHSD) of the aldo-keto reductPalabras claves:Autores:Brandmaier A., Papari-Zareei M., Richard J. AuchusFuentes:scopusPhenotypic variation in a Chinese family with 46,XY and 46,XX 17α-hydroxylase deficiency
ArticleAbstract: Background: 17α-hydroxylase deficiency is a rare autosomal recessive disorder characterized by sexuaPalabras claves:17α-hydroxylase deficiency, CYP17A1 gene, Cytochrome P450c17, Mutational analysis, phenotypic variationAutores:Bee Y.M., Manju C., Papari-Zareei M., Richard J. AuchusFuentes:scopus3β-hydroxysteroid dehydrogenase is a possible pharmacological target in the treatment of castration-resistant prostate cancer
ArticleAbstract: Prostate cancer usually responds to androgen deprivation therapy, although the response in metastatiPalabras claves:Autores:Evaul K., Li R., Papari-Zareei M., Richard J. Auchus, Sharifi N.Fuentes:scopusCombined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patien
ArticleAbstract: Congenital adrenal hyperplasia (CAH) resulting from 17α-hydroxylase/17,20-lyase deficiency is a rarePalabras claves:Autores:Costenaro F., Czepielewski M., Kater C.E., Papari-Zareei M., Richard J. Auchus, Rodrigues T.Fuentes:scopusTwo novel mutations found in a patient with 17α-hydroxylase enzyme deficiency
ArticleAbstract: Context: Congenital adrenal hyperplasia resulting from 17α- hydroxylase deficiency (17OHD) is a rarePalabras claves:Autores:Ergun-Longmire B., New M., Papari-Zareei M., Richard J. Auchus, Tansil S., Wilson R.Fuentes:scopus