Homodimerisation-independent cleavage of dsRNA by a pestiviral nicking endoribonuclease

por Lussi, Carmela, Sauter, Kay-Sara, Schweizer, Matthias
Publicado 2018

MON-219 In Silico and in Vitro Studies of Human 5α-Reductase Type II Variants in Search for Activating Variants Explaining Androgen Excess Reveal New Loss-Of-Function Variants

por Katharopoulos, Efstathios, Sauter, Kay, Pandey, Amit, Flueck, Christa
Publicado 2019

Resveratrol inhibits androgen production of human adrenocortical H295R cells by lowering CYP17 and CYP21 expression and activities

por Marti, Nesa, Bouchoucha, Nadia, Sauter, Kay-Sara, Flück, Christa E.
Publicado 2017

Complete Genome Sequences of Both Biotypes of a Virus Pair of Bovine Viral Diarrhea Virus Subgenotype 1k

por Marques Antunes de Oliveira, Adriano, Stalder, Hanspeter, Peterhans, Ernst, Sauter, Kay-Sara, Schweizer, Matthias
Publicado 2013

Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease

por Flück, Christa E., Audí, Laura, Fernández-Cancio, Mónica, Sauter, Kay-Sara, Martinez de LaPiscina, Idoia, Castaño, Luis, Esteva, Isabel, Camats, Núria
Publicado 2019

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

Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1

por Martínez de LaPiscina, Idoia, Mahmoud, Rana AA, Sauter, Kay-Sara, Esteva, Isabel, Alonso, Milagros, Costa, Ines, Rial-Rodriguez, Jose Manuel, Rodríguez-Estévez, Amaia, Vela, Amaia, Castano, Luis, Flück, Christa E.
Publicado 2020

Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation

por Lucas, Cécily, Sauter, Kay-Sara, Steigert, Michael, Mallet, Delphine, Wilmouth, James, Olabe, Julie, Plotton, Ingrid, Morel, Yves, Aeberli, Daniel, Wagner, Franca, Clevers, Hans, Pandey, Amit V., Val, Pierre, Roucher-Boulez, Florence, Flück, Christa E.
Publicado 2023

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

por Martinez de Lapiscina, Idoia, Kouri, Chrysanthi, Aurrekoetxea, Josu, Sanchez, Mirian, Naamneh Elzenaty, Rawda, Sauter, Kay-Sara, Camats, Núria, Grau, Gema, Rica, Itxaso, Rodriguez, Amaia, Vela, Amaia, Cortazar, Alicia, Alonso-Cerezo, Maria Concepción, Bahillo, Pilar, Bertholt, Laura, Esteva, Isabel, Castaño, Luis, Flück, Christa E.
Publicado 2023