Hyperdiploid acute lymphoblastic leukemia in children with <i>LZTR1</i> germline variants-Reference-Cited by-同舟云学术

Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants

Published:2024-01 Issue:1 Volume:8 Page:
ISSN:2572-9241
Container-title:HemaSphere
language:en
Short-container-title:HemaSphere

Author:

Zipper Lisa¹,Wagener Rabea²,Fischer Ute²³,Hoffmann Anna²,Yasin Layal²,Brandes Danielle²,Soura Stavrieta²,Anwar Ammarah²,Walter Carolin⁴,Varghese Julian⁴,Hauer Julia⁵,Auer Franziska⁵,Bhatia Sanil²,Dugas Martin⁶,Junk Stefanie V.²⁷,Stanulla Martin⁷,Haas Oskar A.⁸,Borkhardt Arndt²³^ORCID,Reiff Tobias¹,Brozou Triantafyllia²

Affiliation:

1. Department of Biology, Institute of Genetics, The Faculty of Mathematics and Natural Sciences Heinrich Heine University Düsseldorf Düsseldorf Germany

2. Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty Heinrich Heine University Düsseldorf Düsseldorf Germany

3. German Cancer Consortium (DKTK) partner site Essen/Düsseldorf Düsseldorf Germany

4. Institute of Medical Informatics University of Münster Münster Germany

5. Department of Pediatrics School of Medicine, Technical University of Munich Munich Germany

6. Institute of Medical Informatics Heidelberg University Hospital Heidelberg Germany

7. Department of Pediatric Hematology and Oncology Hannover Medical School Hannover Germany

8. St. Anna Children's Hospital, Pediatric Clinic Medical University Vienna Austria

Funder

Deutsche Forschungsgemeinschaft

Wilhelm Sander-Stiftung

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hem3.26

Reference14 articles.

1. Hyperdiploidy: the longest known, most prevalent, and most enigmatic form of acute lymphoblastic leukemia in children

2. Acute lymphoblastic leukemia in the context of RASopathies

3. LZTR1 is a regulator of RAS ubiquitination and signaling

4. Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

5. EGFR signaling activates intestinal stem cells by promoting mitochondrial biogenesis and β-oxidation