
Diwan, Gaurav Dr.Universität HeidelbergHeidelberg
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- Strähle, Uwe (1)
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Publications in heiBIB 
- Rezi, Csenge K.: DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2 / Csenge K Rezi, Mariam G Aslanyan, Gaurav D Diwan, Tao Cheng, Mohamed Chamlali, Katrin Junger, Zeinab… , 7 June 2024. - 24 S. : Illustrationen
In: EMBO reports, ISSN 1469-3178. 25(2024), 7, Seite 3040-3063
DOI: 10.1038/s44319-024-00170-1
- André, Timon: Reduced protein stability of 11 pathogenic missense STXBP1/MUNC18-1 variants and improved disease prediction / Timon André, Annemiek A. van Berkel, Gurdeep Singh, Esam T. Abualrous, Gaurav D. Diwan, Torsten Schm… , 15 July 2024. - 12 S. : Illustrationen
In: Biological psychiatry, ISSN 1873-2402. 96(2024), 2 vom: Juli, Seite 125-136
DOI: 10.1016/j.biopsych.2024.03.007
- Ellermann, Julia: Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions / Julia Schöpf, Sebastian Uhrig, Christoph E. Heilig, Kwang-Seok Lee, Tatjana Walther, Alexander Caraz… , 02 January 2024. - 17 S.
In: Nature Communications, ISSN 2041-1723. 15(2024), Artikel-ID 51, Seite 1-17
DOI: 10.1038/s41467-023-44360-2
- Freke, Grace Mercedes: De-Suppression of mesenchymal cell identities and variable phenotypic outcomes associated with knockout of Bbs1 / Grace Mercedes Freke, Tiago Martins, Rosalind Jane Davies, Tina Beyer, Marian Seda, Emma Peskett, Na… , 20 November 2023. - 21 S. : Illustrationen
In: Cells, ISSN 2073-4409. 12(2023), 22, Artikel-ID 2662, Seite 1-21
DOI: 10.3390/cells12222662
- Sane, Mrudula: Shifts in mutation spectra enhance access to beneficial mutations / Mrudula Sane, Gaurav D. Diwan, Bhoomika A. Bhat, Lindi M. Wahl, and Deepa Agashe, May 30, 2023. - 11 S. : Illustrationen
In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 1091-6490. 120(2023), 22, Artikel-ID e2207355120, Seite 1-11
DOI: 10.1073/pnas.2207355120
- Colbourne, John: The Precision Toxicology initiative / The PrecisionTox Consortium*, 1 July 2023. - 10 S. : Illustrationen
In: Toxicology letters, ISSN 1879-3169. 383(2023) vom: Juli, Seite 33-42
DOI: 10.1016/j.toxlet.2023.05.004
- Schmenger, Torsten: Never-homozygous genetic variants in healthy populations are potential recessive disease candidates / Torsten Schmenger, Gaurav D. Diwan, Gurdeep Singh, Gordana Apic and Robert B. Russell, 08 September 2022. - 7 S.
In: npj Genomic Medicine, ISSN 2056-7944. 7(2022), Seite 1-7
DOI: 10.1038/s41525-022-00322-z
- Staufner, Christian: Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients / Christian Staufner, MD, Bianca Peters, Matias Wagner, MD, Seham Alameer, MD, Ivo Barić, MD, PhD, Pie… , 2020. - 12 S.
In: Genetics in medicine, ISSN 1530-0366. 22(2020), 3, Seite 610-621
DOI: 10.1038/s41436-019-0698-4
