Check biochemistry, genetics and molecular biology papers: citations, claims and retractions

Alternative polyadenylation diversifies post‐transcriptional regulation by selective RNA–protein interactions

Gupta, I., Clauder‐Münster, S., Klaus, B., Järvelin, A. I., Aiyar, R. S., Benes, V., Wilkening, S., Huber, W., Pelechano, V., & Steinmetz, L. M. (2014) · Molecular Systems Biology

RNA Research and SplicingRNA and protein synthesis mechanisms

Cited by 95

Specification of Individual Adult Motor Neuron Morphologies by Combinatorial Transcription Factor Codes

Enriquez, J., Venkatasubramanian, L., Baek, M., Peterson, M., Aghayeva, U., & Mann, R. S. (2015) · Neuron

Developmental Biology and Gene RegulationNeurobiology and Insect Physiology Research

Cited by 95

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

Schwarz, N., Hahn, A., Bast, T., Müller, S., Löffler, H., Maljevic, S., Gaily, E., Prehl, I., Biskup, S., Joensuu, T., et al. (2016) · Journal of Neurology

Ion channel regulation and functionEpilepsy research and treatment

Cited by 95

Author Correction: Effect of long-term caloric restriction on DNA methylation measures of biological aging in healthy adults from the CALERIE trial

Waziry, R., Ryan, C. P., Corcoran, D. L., Huffman, K. M., Kobor, M. S., Kothari, M., Graf, G. H., Kraus, V. B., Kraus, W. E., Lin, D. T. S., et al. (2023) · Nature Aging

Epigenetics and DNA MethylationGenetics, Aging, and Longevity in Model Organisms

Cited by 95

Nucleolar dominance: a model for rRNA gene silencing

McStay, B. (2006) · Genes & Development

Genomics and Chromatin DynamicsNuclear Structure and Function

Cited by 95

Mitochondrial DNA deletions cause the biochemical defect observed in Alzheimer’s disease

Krishnan, K. J., Ratnaike, T. E., De Gruyter, H. L. M., Jaros, E., & Turnbull, D. M. (2012) · Neurobiology of Aging

Mitochondrial Function and PathologyAlzheimer's disease research and treatments

Cited by 95

Structural insights into the interaction and activation of histone deacetylase 3 by nuclear receptor corepressors

Codina, A., Love, J. D., Li, Y., Lazar, M. A., Neuhaus, D., & Schwabe, J. W. R. (2005) · Proceedings of the National Academy of Sciences

Histone Deacetylase Inhibitors ResearchGenomics and Chromatin Dynamics

Cited by 95

Age‐related loss of nitric oxide synthase in skeletal muscle causes reductions in calpain S‐nitrosylation that increase myofibril degradation and sarcopenia

Samengo, G., Avik, A., Fedor, B., Whittaker, D., Myung, K. H., Wehling‐Henricks, M., & Tidball, J. G. (2012) · Aging Cell

Muscle Physiology and DisordersNutrition and Health in Aging

Cited by 95

ChIP bias as a function of cross-linking time

Baranello, L., Kouzine, F., Sanford, S., & Levens, D. (2016) · Chromosome Research

Genomics and Chromatin DynamicsChromatin Remodeling and Cancer

Cited by 95

Classification of Dukes' B and C colorectal cancers using expression arrays

Frederiksen, C. M., Knudsen, S., Laurberg, S., & Ørntoft, T. F. (2003) · Journal of Cancer Research and Clinical Oncology

Gene expression and cancer classificationBreast Cancer Treatment Studies

Cited by 95

A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration

Scimone, M. L., Lapan, S. W., & Reddien, P. W. (2014) · PLoS Genetics

Planarian Biology and ElectrostimulationDevelopmental Biology and Gene Regulation

Cited by 95

Dynamic alteration of soluble serum biomarkers in healthy aging

Shurin, G. V., Yurkovetsky, Z. R., Chatta, G. S., Tourkova, I. L., Shurin, M. R., & Lokshin, A. E. (2007) · Cytokine

Genetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and Senescence

Cited by 95

Oestrogen Receptor α Localisation in the Prefrontal Cortex of Three Mammalian Species

Montague, D., Weickert, C. S., Tomaskovic‐Crook, E., Rothmond, D. A., Kleinman, J. E., & Rubinow, D. R. (2008) · Journal of Neuroendocrinology

Estrogen and related hormone effectsNeuroendocrine regulation and behavior

Cited by 95

The origins and formation of bone-resorbing osteoclasts

Elson, A., Anuj, A., Barnea-Zohar, M., & Reuven, N. (2022) · Bone

Bone Metabolism and DiseasesOsteomyelitis and Bone Disorders Research

Cited by 95

Identifying the favored mutation in a positive selective sweep.

Akbari, A., Vitti, J. J., Iranmehr, A., Bakhtiari, M., Sabeti, P. C., Mirarab, S., & Bafna, V. (2018) · Nature Methods

Evolution and Genetic DynamicsGenetic diversity and population structure

Cited by 95

Mechanisms of Hox gene colinearity: transposition of the anterior Hoxb1 gene into the posterior HoxD complex

Kmita, M., van der Hoeven, F., Zákány, J., Krumlauf, R., & Duboule, D. (2000) · Genes & Development

Developmental Biology and Gene RegulationGenomics and Chromatin Dynamics

Cited by 95

Immunomodulation by Bifidobacterium infantis 35624 in the murine lamina propria requires retinoic acid-dependent and independent mechanisms

Konieczna, P., Ferstl, R., Ziegler, M., Frei, R., Nehrbass, D., Lauener, R. P., Akdis, C. A., & O'Mahony, L. (2013) · PLoS ONE

Gut microbiota and healthProbiotics and Fermented Foods

Cited by 95

Macropinocytosis: Insights from immunology and cancer

Stow, J. L., Hung, Y., & Wall, A. A. (2020) · Current Opinion in Cell Biology

Cellular transport and secretionCaveolin-1 and cellular processes

Cited by 95

Calibration of Multiple In Silico Tools for Predicting Pathogenicity of Mismatch Repair Gene Missense Substitutions

Thompson, B. A., Greenblatt, M. S., Vallee, M. P., Herkert, J. C., Tessereau, C., Young, E. L., Adzhubey, I. A., Li, B., Bell, R., Feng, B., et al. (2013) · Human Mutation

Genomics and Rare DiseasesGenetic factors in colorectal cancer

Cited by 95

Mechanisms of nanoparticle-mediated siRNA transfection by melittin-derived peptides

Hou, K. K., Pan, H., Ratner, L., Schlesinger, P. H., & Wickline, S. A. (2013) · ACS Nano

RNA Interference and Gene DeliveryNanoparticle-Based Drug Delivery

Cited by 95

Structural and kinetic analysis of the COP9-Signalosome activation and the cullin-RING ubiquitin ligase deneddylation cycle

Mosadeghi, R., Reichermeier, K. M., Winkler, M., Schreiber, A., Reitsma, J. M., Zhang, Y., Stengel, F., Cao, J., Kim, M., Sweredoski, M. J., et al. (2016) · eLife

Ubiquitin and proteasome pathwaysProtein Degradation and Inhibitors

Cited by 95

Intracranial abnormalities detected by three‐dimensional magnetic resonance imaging in Prader–Willi syndrome

Miller, J. L., Couch, J. A., Schmalfuss, I., He, G., Liu, Y., & Driscoll, D. J. (2007) · American Journal of Medical Genetics Part A

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 95

Pattern of Brachyury gene expression in starfish embryos resembles that of hemichordate embryos but not of sea urchin embryos

Shoguchi, E., Satoh, N., & Maruyama, Y. K. (1999) · Mechanisms of Development

Developmental Biology and Gene RegulationMarine Invertebrate Physiology and Ecology

Cited by 95

Characterization of the myeloid-specific CD11b promoter

Pahl, H., Rosmarin, A., & Tenen, D. (1992) · Blood

Genomics and Chromatin DynamicsCell Adhesion Molecules Research

Cited by 95