:: Library Catalog

Cover Image

Saved in:

Bibliographic Details
Main Author:	Mishra, Aditya
Format:	Recurso digital
Language:
Published:	Zenodo 2026
Online Access:	https://doi.org/10.5281/zenodo.19453042
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Repaglinide Revisited: A Temporal Insulin Alignment Hypothesis for β-Cell Preservation and Metabolic Efficiency in Type 2 Diabetes Mellitus
by: Mishra, Aditya
Published: (2026)

A Multi‐Phenotype Approach to Joint Testing of Main Genetic and Gene‐Environment Interaction Effects
by: Saurabh Mishra, et al.
Published: (2025)

Disruption of the l ‐ DOPA Receptor Gpr143/OA1 ‐Gene in Mice Creates a Unique Mixed Psychosis‐Like Phenotype
by: Yoshio Goshima, et al.
Published: (2026)

SGLT‐2 Inhibitors Are Potent to Suppress Aggressive Transformation From Indolent Type of Adult T‐Cell Leukemia/Lymphoma: Unique Insight Into Therapeutics for Diabetes‐Related Hematological Malignancy
by: Kazuho Morichika, et al.
Published: (2025)

Estrogen‐Related Receptor Gamma (ERRγ) as Biomarker and Novel Target for Therapeutic Intervention on Cancer: A Review
by: Priyanka Upadhyay, et al.
Published: (2024)

Mendelian Randomization Identified SLC2A9 as a Novel cis‐eQTL‐Mediated Susceptibility Gene in Suppressing Renal Cancer and Its Related Metabolic Mechanisms
by: Yi Wang, et al.
Published: (2026)

A Necessary and Sufficient Condition for Uniqueness of Euclidean Division
by: Sekhon, Senan
Published: (2026)

Identification and Validation of the Ferroptosis‐Related Gene SLC2A1 as a Novel Prognostic Biomarker for Osimertinib Resistance in LUAD
by: Lixia Zhang, et al.
Published: (2026)

Real‐World Effectiveness of SGLT2 Inhibitors Across Heart Failure Phenotypes: A Meta‐Analysis
by: Mohammed Elmujtba A. E, et al.
Published: (2026)

The Importance of Newborn Genetic Screening for Early Identification of GJB2 and SLC26A4 Related Hearing Loss
by: Emily R Wener, et al.
Published: (2025)

Expanding the Phenotype of Syndromic SLC30A9 ‐Associated Disease
by: Naomi E. Wagner, et al.
Published: (2025)

Pan‐Cancer Analysis and Functional Characterization Identify SLC15A4 as a Novel Prognostic Biomarker and Therapeutic Target
by: Xiaodan Lyu, et al.
Published: (2026)

Birkhoff's Theorem and Uniqueness: A Peek Beyond General Relativity
by: Ghosh, Rajes, et al.
Published: (2024)

A Missense Variant in the IKZF2 Gene Identified in a Genetically Undiagnosed Family With Hearing Loss
by: Teng Zhang, et al.
Published: (2025)

Novel Homozygous Full Gene Deletion of SLC12A5 in a Newborn With Refractory Seizures
by: Lauren M. Wainman, et al.
Published: (2025)

Improvement of Motor Function in SLC39A8‐Related Ataxia Through Manganese Supplementation: A Therapeutic Insight
by: Denise Maria Meneses Cury Portela, et al.
Published: (2025)

Comprehensive Investigation of Proteoglycan Gene Expression in Breast Cancer: Discovery of a Unique Proteoglycan Gene Signature Linked to the Malignant Phenotype
by: Simone Buraschi, et al.
Published: (2025)

Novel Variants in the SLC16A2 Gene Associated With Allan–Herndon–Dudley Syndrome in China
by: Wei Li, et al.
Published: (2026)

Chronic Diarrhoea in Children: The Role of SLC10A2 Gene in Primary Malabsorption of Biliary Acid
by: Marika Comegna, et al.
Published: (2026)

SGLT2 Inhibitors and GLP‐1 Receptor Agonists After Acute Kidney Injury: A Systematic Review With Meta‐Analysis
by: Erin F. Barreto, et al.
Published: (2026)

Genotype and Clinical Phenotype of Monocarboxylate Transporter 1 Deficiency in Three Palestinian Children: Report of Two Novel Variants in the SLC16A1 Gene
by: Imad Dweikat, et al.
Published: (2025)

Association in Facial Phenotype, Gene, Disease: A Dataset for Explainable Rare Genetic Diseases Diagnosis
by: Song, Jie, et al.
Published: (2025)

Therapeutic targeting in HER2+ breast cancer to prevent and treat CNS disease: SLC1A1.
by: Mamoor, Shahan
Published: (2025)

Gonadal Development–Related Genes and a Male‐Specific Genetic Marker Identified in the Endangered Sichuan Taimen ( Hucho bleekeri )
by: Qinyao Wei, et al.
Published: (2026)

Phenotypic Characterization of Recently Identified PSEN1 Genetic Variants in ADAD in Colombia
by: Alejandro Guerrero, et al.
Published: (2025)

A Unique Case of MBD5 and CCM2 Deletions Leading to a Severe Neurological Phenotype With Prolonged Status Epilepticus
by: Sebastián Silva, et al.
Published: (2025)

Exonic Deletions and Deep Intronic Variants of the SLC26A4 Gene Contribute to the Genetic Diagnosis of Unsolved Patients With Enlarged Vestibular Aqueduct
by: Yongan Tian, et al.
Published: (2024)

Clinical and Genetic Landscape of IGHMBP2‐Related Disorders: From Novel Variants to Phenotypic Insights
by: Tinatin Tkemaladze, et al.
Published: (2025)

Asparagine transport through SLC1A5/ASCT2 and SLC38A5/SNAT5 is essential for BCP‐ALL cell survival and a potential therapeutic target
by: Giuseppe Taurino, et al.
Published: (2024)

Dormant Metastases Exhibit a Unique Phenotype Primarily Promoted by the Ch25h Gene and Are Maintained in Dormancy by T Lymphocytes
by: Virginia Chamorro, et al.
Published: (2025)

Coagulation Dysfunction Caused by a De Novo Mutation of Gene SLC37A4
by: Mauro Guariento, et al.
Published: (2024)

Identifying Provider Prescribing Practices for GLP‐1RAs and SGLT‐2is in Patients With Type 2 Diabetes to Address Pharmacoinequity
by: Parnnate Wongsirisakul, et al.
Published: (2026)

Letter to the Editor: Interpreting the Clinical Applicability of SGLT ‐2 Inhibitors in MASH ‐Related Cirrhosis
by: Binqi Wang, et al.
Published: (2026)

Comparison of SGLT1, SGLT2, and Dual Inhibitor Biological Activity in Treating Type 2 Diabetes Mellitus
Published: (2024)

SGLT2 Inhibitors as a Therapeutic Option for Both Acute and Chronic Refractory Hypomagnesemia in Diabetic and Nondiabetic Patients: A Multicenter Case Series
by: Fatima Ayub, et al.
Published: (2025)

Identifying Susceptibility Genes and Shared Genetic Architecture for Longevity and Muscle Weakness
by: Yilong Lin, et al.
Published: (2026)

Downstream Treatment Burden and Health‐Care Utilization Following Initiation of GLP ‐1 Receptor Agonists or SGLT2 Inhibitors in Type 2 Diabetes
by: Yazan Alhamdan, et al.
Published: (2026)

Mixed‐Phenotype Acute Leukemia With Mutated TP53 : Genetic Landscape, Therapeutic Response, and Outcomes
by: Wei J. Wang, et al.
Published: (2025)

Genotype–Phenotype Correlation in Germline TSH Receptor Activating Mutation Associated Hyperthyroidism: A Systematic Review
by: Chethan Yamichannaiah, et al.
Published: (2025)

The Sufficient and Necessary Condition for the Identifiability and Estimability of the DINA Model
by: Gu, Yuqi, et al.
Published: (2017)