Pharmacogenomics of human P450 oxidoreductase

por Pandey, Amit V., Sproll, Patrick
Publicado 2014

PMON52 Use of PDE5 Inhibitors as Potential Treatment for Isolated Growth Hormone Deficiency Caused by Alternate Splicing of GH1 Gene

por Pandey, Amit V, Velazquez, Maria Natalia Rojas
Publicado 2022

Bioactivity of Curcumin on the Cytochrome P450 Enzymes of the Steroidogenic Pathway

por Castaño, Patricia Rodríguez, Parween, Shaheena, Pandey, Amit V
Publicado 2019

Altered CYP19A1 and CYP3A4 Activities Due to Mutations A115V, T142A, Q153R and P284L in the Human P450 Oxidoreductase

por Udhane, Sameer S., Parween, Shaheena, Kagawa, Norio, Pandey, Amit V.
Publicado 2017

Loss of Protein Stability and Function Caused by P228L Variation in NADPH-Cytochrome P450 Reductase Linked to Lower Testosterone Levels

por Rojas Velazquez, Maria Natalia, Noebauer, Mathias, Pandey, Amit V.
Publicado 2022

Retinoic acid receptor beta and angiopoietin-like protein 1 are involved in the regulation of human androgen biosynthesis

por Udhane, Sameer S., Pandey, Amit V., Hofer, Gaby, Mullis, Primus E., Flück, Christa E.
Publicado 2015

Variability in Loss of Multiple Enzyme Activities Due to the Human Genetic Variation P284T Located in the Flexible Hinge Region of NADPH Cytochrome P450 Oxidoreductase

por Parween, Shaheena, Rojas Velazquez, Maria Natalia, Udhane, Sameer S., Kagawa, Norio, Pandey, Amit V.
Publicado 2019

Variant predictions in congenital adrenal hyperplasia caused by mutations in CYP21A2

por Prado, Mayara J., Ligabue-Braun, Rodrigo, Zaha, Arnaldo, Rossetti, Maria Lucia Rosa, Pandey, Amit V.
Publicado 2022

Editorial: Role of Protein-Protein Interactions in Metabolism: Genetics, Structure, Function

por Pandey, Amit V., Henderson, Colin J., Ishii, Yuji, Kranendonk, Michel, Backes, Wayne L., Zanger, Ulrich M.
Publicado 2017

Non-steroidal CYP17A1 Inhibitors: Discovery and Assessment

por Wróbel, Tomasz M., Jørgensen, Flemming Steen, Pandey, Amit V., Grudzińska, Angelika, Sharma, Katyayani, Yakubu, Jibira, Björkling, Fredrik
Publicado 2023

Recognition of fold- and function-specific sites in the ligand-binding domain of the thyroid hormone receptor-like family

por Verma, Sonia, Chakraborti, Soumyananda, Singh, Om P., Pande, Veena, Dixit, Rajnikant, Pandey, Amit V., Pandey, Kailash C.
Publicado 2022

MON-LB014 Autosomal Dominant Growth Hormone Deficiency Due to a Novel c.178g>A Mutation in the GH1 Gene Is Caused by Alternative Splicing to Produce a Small GH Isoform

por Miller, Bradley Scott, Rihs, Silvia, Parween, Shaheena, Ternand, Christine, Gregory, Louise Cheryl, Dattani, Mehul Tulsidas, Pandey, Amit V
Publicado 2020

Reducing FASN expression sensitizes acute myeloid leukemia cells to differentiation therapy

por Humbert, Magali, Seiler, Kristina, Mosimann, Severin, Rentsch, Vreni, Sharma, Katyayani, Pandey, Amit V., McKenna, Sharon L., Tschan, Mario P.
Publicado 2021

Novel CYP19A1 Mutations Extend the Genotype-Phenotype Correlation and Reveal the Impact on Ovarian Function

por Praveen, Valiyaparambil Pavithran, Ladjouze, Asmahane, Sauter, Kay-Sara, Pulickal, Annie, Katharopoulos, Efstathios, Trippel, Mafalda, Perren, Aurel, Pandey, Amit V, Flück, Christa E
Publicado 2020

Characterization of Novel StAR (Steroidogenic Acute Regulatory Protein) Mutations Causing Non-Classic Lipoid Adrenal Hyperplasia

por Flück, Christa E., Pandey, Amit V., Dick, Bernhard, Camats, Núria, Fernández-Cancio, Mónica, Clemente, María, Gussinyé, Miquel, Carrascosa, Antonio, Mullis, Primus E., Audi, Laura
Publicado 2011

Mechanism of the Dual Activities of Human CYP17A1 and Binding to Anti-Prostate Cancer Drug Abiraterone Revealed by a Novel V366M Mutation Causing 17,20 Lyase Deficiency

por Fernández-Cancio, Mónica, Camats, Núria, Flück, Christa E., Zalewski, Adam, Dick, Bernhard, Frey, Brigitte M., Monné, Raquel, Torán, Núria, Audí, Laura, Pandey, Amit V.
Publicado 2018

Synthesis and Structure–Activity Relationships of Novel Non-Steroidal CYP17A1 Inhibitors as Potential Prostate Cancer Agents

por Wróbel, Tomasz M., Rogova, Oksana, Sharma, Katyayani, Rojas Velazquez, Maria Natalia, Pandey, Amit V., Jørgensen, Flemming Steen, Arendrup, Frederic S., Andersen, Kasper L., Björkling, Fredrik
Publicado 2022

Characterization of Mutations Causing CYP21A2 Deficiency in Brazilian and Portuguese Populations

por Prado, Mayara J., Singh, Shripriya, Ligabue-Braun, Rodrigo, Meneghetti, Bruna V., Rispoli, Thaiane, Kopacek, Cristiane, Monteiro, Karina, Zaha, Arnaldo, Rossetti, Maria L. R., Pandey, Amit V.
Publicado 2021

Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia

por Katharopoulos, Efstathios, Di Iorgi, Natascia, Fernandez-Alvarez, Paula, Pandey, Amit V., Groessl, Michael, Dubey, Shraddha, Camats, Núria, Napoli, Flavia, Patti, Giuseppa, Lezzi, Marilea, Maghnie, Mohamad, Flück, Christa E.
Publicado 2020

GATA4 Variants in Individuals With a 46,XY Disorder of Sex Development (DSD) May or May Not Be Associated With Cardiac Defects Depending on Second Hits in Other DSD Genes

por Martinez de LaPiscina, Idoia, de Mingo, Carmen, Riedl, Stefan, Rodriguez, Amaia, Pandey, Amit V., Fernández-Cancio, Mónica, Camats, Nuria, Sinclair, Andrew, Castaño, Luis, Audi, Laura, Flück, Christa E.
Publicado 2018