# XCell Science (United States)

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/xcell-science-united-states/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 93 |
| Citations | 10,713 |
| City | Novato |
| Country | US |
| Description | XCell Science (United States) is a research organisation in Novato, US. OpenAlex records 211 works and 10,713 citations for it. 104 researchers list it as their most recent affiliation. |
| Homepage | http://www.xcellscience.com/ |
| OpenAlex ID | https://openalex.org/I4210125614 |
| Region | California |
| Researchers | 104 |
| ROR ID | https://ror.org/02vnj6d40 |
| Type | company |
| Works | 211 |

## University papers

- [The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore](https://scholariq.org/papers/the-adp-atp-translocator-is-not-essential-for-the-mitochondrial-permeability/)
- [Experimentally Derived Metastasis Gene Expression Profile Predicts Recurrence and Death in Patients With Colon Cancer](https://scholariq.org/papers/experimentally-derived-metastasis-gene-expression-profile-predicts-recurrence/)
- [Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling](https://scholariq.org/papers/exome-capture-reveals-znf423-and-cep164-mutations-linking-renal-ciliopathies-to/)
- [Proteome analysis of human colon cancer by two‐dimensional difference gel electrophoresis and mass spectrometry](https://scholariq.org/papers/proteome-analysis-of-human-colon-cancer-by-two-dimensional-difference-gel/)
- [ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption](https://scholariq.org/papers/adck4-mutations-promote-steroid-resistant-nephrotic-syndrome-through-coq10/)
- [Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy](https://scholariq.org/papers/candidate-exome-capture-identifies-mutation-of-sdccag8-as-the-cause-of-a-retinal/)
- [ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling](https://scholariq.org/papers/arhgdia-mutations-cause-nephrotic-syndrome-via-defective-rho-gtpase-signaling/)
- [ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6](https://scholariq.org/papers/zmynd10-is-mutated-in-primary-ciliary-dyskinesia-and-interacts-with-lrrc6/)
- [KANK deficiency leads to podocyte dysfunction and nephrotic syndrome](https://scholariq.org/papers/kank-deficiency-leads-to-podocyte-dysfunction-and-nephrotic-syndrome/)

## University top topics

Showing 8 of 25.

- [CAR-T cell therapy research](https://scholariq.org/topics/car-t-cell-therapy-research/)
- [Pluripotent Stem Cells Research](https://scholariq.org/topics/pluripotent-stem-cells-research/)
- [3D Printing in Biomedical Research](https://scholariq.org/topics/3d-printing-in-biomedical-research/)
- [CRISPR and Genetic Engineering](https://scholariq.org/topics/crispr-and-genetic-engineering/)
- [Cancer, Hypoxia, and Metabolism](https://scholariq.org/topics/cancer-hypoxia-and-metabolism/)
- [Cancer Research and Treatments](https://scholariq.org/topics/cancer-research-and-treatments/)
- [Nerve injury and regeneration](https://scholariq.org/topics/nerve-injury-and-regeneration/)
- [Monoclonal and Polyclonal Antibodies Research](https://scholariq.org/topics/monoclonal-and-polyclonal-antibodies-research/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.