National Institute for Biotechnology and Genetic Engineering
22 imported, source-linked research records. All imported publication dates.
22 matching research records
Only records linked to National Institute for Biotechnology and Genetic Engineering are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.
Showing 1–22 of 22 matching records. Counts update as records arrive.
Immunoregulatory Biomaterials for Bone Tissue Engineering: Mechanisms, Design Strategies and Translational Challenges
August 3, 2026 · 0 citations · Open access
Open original record →Emerging biomaterials for next-generation wound healing: From infection control to tissue regeneration
May 19, 2026 · 0 citations
Open original record →Advancements and Challenges in Anti-aging Research: Exploring Anti-aging Pathways to Longevity and Disease Prevention
December 30, 2025 · 0 citations · Open access
Open original record →Recommendations for sample selection, collection and preparation for NMR-based metabolomics studies of blood
May 10, 2025 · 36 citations · Open access
Open original record →Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects
September 18, 2024 · 4 citations · Open access
Open original record →Advancements in Immunotherapeutic Treatments for Hepatocellular Carcinoma: Potential of Combination Therapies
June 21, 2024 · 15 citations · Open access
Open original record →ADVANCES IN CARDIAC REGENERATIVE MEDICINE: EMERGING THERAPIES AND TRANSLATIONAL POTENTIAL
April 30, 2024 · 0 citations · Open access
Open original record →Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome
December 20, 2023 · 9 citations · Open access
Open original record →Mechanism of the antidiabetic action of Nigella sativa and Thymoquinone: a review
September 25, 2023 · 45 citations · Open access
Open original record →Exome sequencing in a Romanian Bardet‐Biedl syndrome cohort revealed an overabundance of causal BBS12 variants
June 9, 2023 · 12 citations · Open access
Open original record →Dihydropyrazole Derivatives Act as Potent α-Amylase Inhibitors and Free Radical Scavengers: Synthesis, Bioactivity Evaluation, Structure–Activity Relationship, ADMET, and Molecular Docking Studies
June 2, 2023 · 25 citations · Open access
Open original record →Whole-Genome Analyses Reveal Genomic Characteristics and Selection Signatures of Lincang Humped Cattle at the China–Myanmar Border
March 22, 2022 · 15 citations · Open access
Open original record →Toward a CRISPR-Cas9-Based Gene Drive in the Diamondback Moth Plutella xylostella
March 14, 2022 · 64 citations · Open access
Open original record →Identification of three novel pathogenic mutations in cystathionine beta-synthase gene of Pakistani intellectually disabled patients
December 14, 2021 · 9 citations · Open access
Open original record →Towards CRISPR/Cas9-based gene drive in the diamondback moth Plutella xylostella
October 5, 2021 · 1 citations · Open access
Open original record →A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family
September 24, 2021 · 6 citations · Open access
Open original record →Understanding divergent domestication traits from the whole-genome sequencing of swamp- and river-buffalo populations
February 14, 2020 · 78 citations · Open access
Open original record →Advancement of Bio inks in three Dimensional Bioprinting
December 3, 2018 · 5 citations · Open access
Open original record →In silico identification of conserved miRNAs and their selective target gene prediction in indicine (Bos indicus) cattle
October 26, 2018 · 16 citations · Open access
Open original record →Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome
September 3, 2018 · 140 citations · Open access
Open original record →Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies
January 1, 2016 · 133 citations · Open access
Open original record →Targeted and Genomewide NGS Data Disqualify Mutations inMYO1A, the “DFNA48Gene”, as a Cause of Deafness
February 25, 2014 · 40 citations · Open access
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