Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and ASCC1[original query] |
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| A Truncated Variant of ASCC1, a Novel Inhibitor of NF-?B, Is Associated with Disease Severity in Patients with Rheumatoid Arthritis. Journal of immunology (Baltimore, Md. : 1950) 2015 Oct . Torices Silvia, Alvarez-Rodríguez Lorena, Grande Lara, Varela Ignacio, Muñoz Pedro, Pascual Dora, Balsa Alejandro, López-Hoyos Marcos, Martinez-Taboada Víctor, Fernández-Luna Jose |
| Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis. Prenatal diagnosis 2021 Jul . Correa Alec Reginald Errol, Naini Kamal, Mishra Pallavi, Dadhwal Vatsla, Agarwal Ramesh, Shukla Rashmi, Kabra Madhulika, Gupta Neer |
| Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European journal of medical genetics 2022 6 65 (8): 104537. Marais Anett, Bertoli-Avella Aida M, Beetz Christian, Altunoglu Umut, Alhashem Amal, Mohamed Sarar, Alghamdi Abdulaziz, Willems Patrick, Tsoutsou Eirini, Fryssira Helena, Pons Roser, Almarzooq Reem, Karatoprak Elif Yüksel, Ayaz Akif, Ünverengil Gökçen, Calvo Maria, Yüksel Zafer, Bauer Pet |
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