Evidence map›Paper›PMID 37603219›Full record

ArticleHuman cell2023

Establishment and characterization of CSCRi006-A: an induced pluripotent stem cell line generated from a patient with Diamond-Blackfan Anemia (DBA) carrying ribosomal protein S19 (RPS19) mutation.

Sonam Rani, Vasanth Thamodaran, Krittika Nandy, N A Fouzia, Madhavi Maddali, Praveena Rajesh, S Vijayanand, Ernest David, Shaji R Velayudhan

Abstract read
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In one paragraph

Article in Human cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Sonam RaniCentre for Stem Cell Research, Christian Medical College, Vellore, India.ORCID http://orcid.org/0000-0002-1556-0647
Vasanth ThamodaranCentre for Stem Cell Research, Christian Medical College, Vellore, India.
Krittika NandyCentre for Stem Cell Research, Christian Medical College, Vellore, India.
N A FouziaDepartment of Hematology, Christian Medical College, Vellore, India.
Madhavi MaddaliDepartment of Hematology, Christian Medical College, Vellore, India.
Praveena RajeshCentre for Stem Cell Research, Christian Medical College, Vellore, India.
S VijayanandDepartment of Biotechnology, Thiruvalluvar University, Vellore, India.
Ernest DavidDepartment of Biotechnology, Thiruvalluvar University, Vellore, India.
Shaji R VelayudhanCentre for Stem Cell Research, Christian Medical College, Vellore, India. rvshaji@cmcvellore.ac.in.ORCID http://orcid.org/0000-0002-8600-2933
Christian Medical College, Vellore · INThiruvalluvar University · IN

Funding

Department of Biotechnology, Ministry of Science and Technology, India BT/PR17316/MED/31/326/2015DST-INSPIRE IF170303Indian Council of Medical Research 2012-1523The Wellcome Trust DBT India Alliance IA/S/17/1/503118
6 · The paper itself

Abstract

Diamond-Blackfan anemia (DBA) is a congenital hypoplastic anemia characterized by ineffective erythropoiesis. DBA is majorly caused by mutations in the ribosomal protein (RP) genes (Gadhiya and Wills in Diamond-Blackfan Anemia, https://www.statpearls.com/ ; 2023). A suitable disease model that yields a continuous supply of erythroid cells is required to study disease pathogenesis and drug discovery. Toward this, we reprogrammed dermal fibroblasts from a DBA patient with a heterozygous mutation c.22-23delAG in the RPS19 gene identified through exome sequencing. To generate induced pluripotent stem cells (iPSCs), we induced episomal expression of the reprogramming factors OTC3/4, L-MYC, LIN28, SOX2, and KLF4, and a p53 shRNA

Indexed as

Anemia, Diamond-BlackfanInduced Pluripotent Stem CellsMutationRibosomal ProteinsCell DifferentiationCell LineCells, CulturedCellular ReprogrammingFibroblastsHumansKruppel-Like Factor 4KLF4 protein, humanKruppel-Like Factor 4Ribosomal Proteinsribosomal protein S19DBADisease modelingEpisomalFibroblastsIPS cells

Identifiers

PMID37603219
OpenAlexW4386019665

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.