KARAMBIOSCIENCE
EST. 2026
EVIDENCE / 02
Separate concept scenes for population biology, pet preservation, biological records and governance.
CRISPR / Source register

The source trail stays visible.

45 references from the CRISPR Project Assessment. Publication dates, source types and review access are not interchangeable.

Concept illustration / not experimental evidence
How to read this collection

Recent findings. Dated context. No hidden upgrades.

The supplied report prioritizes 2026, especially July 15–October 15, and explicitly includes earlier background. This register preserves that distinction.

Most research briefs in this release are assessment-derived, not newly full-text reviewed. Limited publication, software-rights and institutional checks are identified in the relevant record. A citation is not evidence that Karam reproduced a study or owns the underlying technology.

New verification note: the OptiPrime publisher statement describes noncommercial-use restrictions. The FDA safety-guidance landing page remains marked draft and nonbinding. Broad’s licensing page addresses one institution’s policy. These checks supplement the supplied report; they do not replace its research assessment.
C01 / Research paper

Yin J, Gao Y, Jing Y, et al. CRISPR screening identifies GNPTAB as a noncanonical STING activator driving cellular senescence. Protein & Cell. 27 July 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C02 / Research paper

Chen ACY, Ji KY, Yerinde C, et al. CRISPR screens identify targets to rescue age-related T cell dysfunction in cancer. Cell. 29 July 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C03 / Research paper

Plesa AM, Jung S, Wang HH, et al. Transcriptomic reprogramming screen identifies SRSF1 as a regulator of aging. Nature Aging. 14 October 2026;6:2057–2073.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C04 / Research paper

Yu T, Ji M, Yu D, et al. Structure-guided discovery and engineering of miniature CRISPR–Cas12m for epigenome editing. Nature Structural & Molecular Biology. 16 September 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C05 / Research paper

Hsu A, Chen PJ, Li AH, et al. Mechanistic machine learning for prediction of prime editing outcomes. Nature Biotechnology. 12 August 2026.

Publisher code-availability statement checked on 15 October 2026. It describes OptiPrime code and hosted service as noncommercial-use only.

Open original source ↗
C06 / Research paper

Madsen A, Selfjord N, Martinez-Lage M, et al. Single-cell and in vivo profiling reveal heterogeneous and organ-specific CRISPR-Cas9 off-target and translocation outcomes. Nature Communications. 26 August 2026;17:9067.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C07 / Research paper

Hwang GH, Vyshedskiy B, Barry T, et al. Analysing long-read CRISPR experiments with CRISPRLungo. Nature Biomedical Engineering. 20 August 2026.

Author-laboratory publication abstract, repository and browser-tool page located on 15 October 2026; no independent software performance test.

Open original source ↗
C08 / Research paper

Jung H, Devant P, Ching C, et al. Virus-like particles enable targeted gene engineering and pooled CRISPR screening in primary human myeloid cells. Nature Biotechnology. 17 August 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C09 / Research paper

Jung H, Jeong B, Kim YW, et al. Precise genomic integration of large DNA fragments by donor-directed annealing using prime editing. Nature Biotechnology. 28 August 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C10 / Research paper

Gu D, Kim GWD, Park M, et al. Abasic CRISPR RNAs inherently harness fidelity of SpCas9 for genome editing. Nature Chemical Biology. 5 February 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C11 / Research paper

Saroj N, Velangani HG, Kiran S, Dholaniya PS. Deletion of TOP2B promoter using CRISPR-Cas9 induces senescence in HEK 293T cells. Biochemistry and Biophysics Reports. 19 May 2026;46:102620.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C12 / Research paper

Lai C, Fu W, Liu J, et al. LMO7-mediated POLR2A degradation promotes cellular senescence through the MDM4/p53/p21 axis. Cell Death & Disease. 28 March 2026;17:421.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C13 / Research paper

Burr SP, Auckland K, Glynos A, et al. MitoPerturb-Seq identifies gene-specific single-cell responses to mitochondrial DNA depletion and heteroplasmy. Nature Structural & Molecular Biology. 1 April 2026;33:711–723.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C14 / Research paper

Jiang AY, Cristian A, Brooks DL, et al. Efficient prime editing in vivo and in vitro using lipid nanoparticles. Nature Nanotechnology. 15 June 2026;21:1022–1035.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C15 / Research paper

Laffin LJ, Nicholls SJ, Scott RS. Durability of CRISPR-Cas9 Gene Editing Targeting ANGPTL3 with CTX310. New England Journal of Medicine. Online 28 August 2026;395:1343–1345.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C16 / Sponsor / developer / institutional announcement

Life Biosciences. First-in-human data from the ongoing Phase 1 trial of ER-100 in optic neuropathies. Sponsor announcement. 8 October 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C17 / Project / institutional / provider context

US Food and Drug Administration. FDA Approves First Gene Therapy for Young Children with Sickle Cell Disease. FDA announcement. 1 July 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C18 / Sponsor / developer / institutional announcement

Intellia Therapeutics. FDA lift of clinical hold on MAGNITUDE Phase 3 clinical trial in ATTR-CM. Sponsor announcement. 2 March 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C19 / Project / institutional / provider context

US Food and Drug Administration. Safety Assessment of Genome Editing in Human Gene Therapy Products Using Next-Generation Sequencing. Draft guidance. April 2026.

FDA guidance landing page checked on 15 October 2026: marked Draft, not for implementation, nonbinding.

Open original source ↗
C20 / Trial registry; not efficacy evidence

ClinicalTrials.gov; Life Biosciences sponsor record. Evaluating ER-100 for Safety in People With Glaucoma or Non-Arteritic Anterior Ischemic Optic Neuropathy. NCT07290244. Reviewed 15 October 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C21 / Project / institutional / provider context

Broad Institute. Licensing gene editing systems. Current institutional policy reviewed 15 October 2026; administrative context.

Broad Institute licensing policy page checked on 15 October 2026. This is one licensor’s policy, not a complete freedom-to-operate opinion.

Open original source ↗
C22 / Research paper

Henard JM, Lee SA, Yu YC, Shao D, Azad RK, Henard CA. CRISPRi-based functional genomic screening identifies genes essential for CH4-dependent growth in a methanotrophic bacterium. Science Advances. 24 April 2026;12:eaed4234.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C23 / Research paper

Groover ED, Ding D, Wang FZ, et al. Mapping cis-regulatory mutations at scale in sorghum enables modulation of gene expression. Nature Biotechnology. 27 March 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C24 / Research paper

Shi LD, Ercoli MF, Kim J, et al. Reduced methane emissions in transgenic rice genotypes are associated with altered rhizosphere microbial hydrogen cycling. Nature Communications. 26 January 2026;17:2028.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C25 / Research paper

Wang Z, Wang S, Yue Z, et al. WLG coordinates multi-stress tolerance in rice by regulating DST-dependent H2O2 homeostasis and stomatal aperture. Nature Communications. 16 September 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C26 / Research paper

Chang J, Wang D, Yao Z, et al. Wild rice locus enables microbiome re-domestication for enhanced nitrogen-use efficiency. Nature Microbiology. 30 September 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C27 / Research paper

Yamori W, Nakazato I, Qu Y, et al. Chloroplast genome editing of Rubisco boosts photosynthesis and plant growth. Nature Communications. 19 June 2026;17:5066.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C28 / Sponsor / developer / institutional announcement

Innovative Genomics Institute. Support from Google.org for AI science research on microbiomes and agricultural methane. Institutional research announcement. 26 January 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C29 / Project / institutional / provider context · Earlier foundational context

National Institutes of Health. Notice of Revisions to the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules. NOT-OD-24-093. 4 April 2024; effective 30 September 2024. Established governance context.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C30 / Project / institutional / provider context · Earlier foundational context

World Health Organization. Guidance framework for testing of genetically modified mosquitoes, second edition. 19 May 2021. Established guidance, not a 2026 research result.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C31 / Research paper

Feng X, Ding J, Liu Y, et al. Self-limiting population suppression gene drive design in the West Nile vector mosquito, Culex quinquefasciatus. Nature Communications. First published 26 May 2026;17:6847.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C32 / Research paper

Kim IK, Tian L, Chaffee R, et al. Seed dormancy shapes gene drive dynamics in plants. Nature Plants. 3 April 2026;12:735–749. Modeling study.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C33 / Sponsor / developer / institutional announcement

Target Malaria. Common questions about gene drive, answered. Developer statement. 30 March 2026; status claims are specific to that date.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C34 / Project / institutional / provider context

The Royal Society. Genetic technologies. Institutional overview reviewed 15 October 2026; proposed applications, not field validation.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C35 / Research paper

Symons TL, Moran A, Balzarolo A, et al. Projected impacts of climate change on malaria in Africa. Nature. 28 January 2026;651:390–396. Modeling study.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C36 / Research paper

Maull V, Aguadé-Gorgorió G, de Lorenzo V, Solé R. Synthetic horizontal gene transfer for ecosystem restoration. Biology Direct. 14 August 2026. Accepted article; theoretical modeling.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C37 / Research paper · Earlier foundational context

Esvelt KM, Smidler AL, Catteruccia F, Church GM. Concerning RNA-guided gene drives for the alteration of wild populations. eLife. 2014;3:e03401. Foundational proposal, not recent deployment evidence.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C38 / Project / institutional / provider context

US Food and Drug Administration. Myths about Cloning. Institutional explanation reviewed 15 October 2026. Primarily livestock context.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C39 / Project / institutional / provider context

ViaGen Pets. How To Clone A Dog: What to Expect & Do Before You Commit. Commercial provider explanation reviewed 15 October 2026; not an independent efficacy evaluation.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C40 / Project / institutional / provider context

ViaGen Pets. Can you clone a dog after death? Commercial provider explanation reviewed 15 October 2026; sample feasibility is case-specific.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C41 / Project / institutional / provider context

US Food and Drug Administration. A Primer on Cloning and Its Use in Livestock Operations. Established SCNT explanation reviewed 15 October 2026; livestock findings are not pet-specific success rates.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C42 / Project / institutional / provider context

Death X. Personal Biological & Digital Archive. Live project page reviewed 15 October 2026; published program edition 14 October 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C43 / Project / institutional / provider context

Death X. Living Cell Banking & Personal Cell Archives. Project proposal published 14 October 2026; reviewed 15 October 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C44 / Project / institutional / provider context

Death X. The Archive & Continuation Research. Live project options reviewed 15 October 2026; Culture remains a contained research concept.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗
C45 / Project / institutional / provider context

Death X. 14 Research Directions for Biological Continuation. Project opportunity map reviewed 15 October 2026.

Cited in the supplied 15 October 2026 project assessment; not independently reviewed in this website release.

Open original source ↗