SCNM1, a Putative RNA Splicing Factor That Modifies Disease Severity in Mice

Initial sequencing and analysis of the human genome

International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216

Efficient selection for high-expression transfectants with a novel eukaryotic vector

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Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

Mammalian Gene Collection (MGC) Program Team* (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242603899 · Cited by 1,756

ESEfinder: a web resource to identify exonic splicing enhancers

Cartegni, L. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg616 · Cited by 1,593

Pre-mRNA splicing and human diseasePreprint

Faustino, N. A., & Cooper, T. A. (2003) · Genes & Development · doi:10.1101/gad.1048803 · Cited by 1,248

Genealogies of mouse inbred strains

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Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1

Cartegni, L., & Krainer, A. R. (2002) · Nature Genetics · doi:10.1038/ng854 · Cited by 730

Sodium channel Na v 1.6 is localized at nodes of Ranvier, dendrites, and synapses

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Insertional mutagenesis in zebrafish rapidly identifies genes essential for early vertebrate development

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Genomewide Analysis of mRNA Processing in Yeast Using Splicing-Specific Microarrays

Clark, T. A., Sugnet, C. W., & Ares, M. (2002) · Science · doi:10.1126/science.1069415 · Cited by 411

Splicing in disease: disruption of the splicing code and the decoding machinery

Wang, G., & Cooper, T. A. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2164 · Cited by 1,077

Intermediate Filaments: Molecular Structure, Assembly Mechanism, and Integration Into Functionally Distinct Intracellular Scaffolds

Herrmann, H. O., & Aebi, U. (2004) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.073823 · Cited by 693

Genomic variants in exons and introns: identifying the splicing spoilers

Pagani, F., & Baralle, F. E. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1327 · Cited by 601

Alternative splicing in disease and therapy

Garcia-Blanco, M. A., Baraniak, A. P., & Lasda, E. L. (2004) · Nature Biotechnology · doi:10.1038/nbt964 · Cited by 527

Sodium channel mutations in epilepsy and other neurological disorders

Meisler, M. H. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25466 · Cited by 512

Polarized Domains of Myelinated Axons

Salzer, J. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00628-7 · Cited by 416

Voltage‐gated sodium channels and pain pathways

Wood, J. N., Boorman, J. P., Okuse, K., & Baker, M. D. (2004) · Journal of Neurobiology · doi:10.1002/neu.20094 · Cited by 377

MATS: a Bayesian framework for flexible detection of differential alternative splicing from RNA-Seq data

Shen, S., Park, J. W., Huang, J., Dittmar, K. A., Lu, Z., Zhou, Q., Carstens, R. P., & Xing, Y. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr1291 · Cited by 373

The neurogenetics of alternative splicing

Vuong, C. K., Black, D. L., & Zheng, S. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.27 · Cited by 340

Genetics of congenital adrenal hyperplasia

Krone, N., & Arlt, W. (2009) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2008.10.014 · Cited by 312

A Genetically Encoded Infrared Probe

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Use of minigene systems to dissect alternative splicing elements

Cooper, T. A. (2005) · Methods · doi:10.1016/j.ymeth.2005.07.015 · Cited by 248

Sodium channelopathies in neurodevelopmental disorders

Meisler, M. H., Hill, S. F., & Yu, W. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00418-4 · Cited by 210

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

Martin, M. S., Tang, B., Papale, L. A., Yu, F. H., Catterall, W. A., & Escayg, A. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm248 · Cited by 202

Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability

O’Brien, J. E., & Meisler, M. H. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00213 · Cited by 158

A Phage Display System with Unnatural Amino Acids

Tian, F., Tsao, M., & Schultz, P. G. (2004) · Journal of the American Chemical Society · doi:10.1021/ja045673m · Cited by 155

Rescue of a human mRNA splicing defect by the plant cytokinin kinetin

Slaugenhaupt, S. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddh046 · Cited by 153

Neuronal proteins custom designed by alternative splicing

Lipscombe, D. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.04.002 · Cited by 145

Site-Specific Incorporation of a Redox-Active Amino Acid into Proteins

Alfonta, L., Zhang, Z., Uryu, S. A., Loo, J. A., & Schultz, P. G. (2003) · Journal of the American Chemical Society · doi:10.1021/ja038242x · Cited by 141

Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Wilson, R. C., Nimkarn, S., Dumić, M., Obeid, J. S., Azar, M. R., Najmabadi, H., Saffari, F., & New, M. I. (2007) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2006.12.005 · Cited by 140

Determinants of the inherent strength of human 5′ splice sites

Roca, X., Sachidanandam, R., & Krainer, A. R. (2005) · RNA · doi:10.1261/rna.2040605 · Cited by 129

Recognition and elimination of nonsense mRNA

Mühlemann, O., EBERLE, A., Stalder, L., & Orozco, R. Z. (2008) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2008.06.012 · Cited by 127

Splicing for alternative structures of Ca1.2 Ca channels in cardiac and smooth muscles

Liao, P. H., Yong, T. A., Liang, M. C., Yue, D. N., & Soong, T. W. (2005) · Cardiovascular Research · doi:10.1016/j.cardiores.2005.06.024 · Cited by 124

Hypomorphic expression ofDkk1in thedoubleridgemouse: dose dependence and compensatory interactions withLrp6

MacDonald, B. T., Adamska, M., & Meisler, M. H. (2004) · Development · doi:10.1242/dev.01126 · Cited by 125

Pathogenic Mechanism of the FIG4 Mutation Responsible for Charcot-Marie-Tooth Disease CMT4J

Lenk, G. M., Ferguson, C., Chow, C. Y., Jin, N., Jones, J. M., Grant, A. E., Zolov, S. N., Winters, J. J., Giger, R. J., Dowling, J. J., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002104 · Cited by 109

Nova2 Interacts with a Cis-Acting Polymorphism to Influence the Proportions of Drug-Responsive Splice Variants of SCN1A

Heinzen, E. L., Yoon, W., Tate, S. K., Sen, A., Wood, N. W., Sisodiya, S. M., & Goldstein, D. B. (2007) · The American Journal of Human Genetics · doi:10.1086/516650 · Cited by 109

mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay

Anderson, J. L., Mulligan, T. S., Shen, M., Wang, H., Scahill, C. M., Tan, F. J., Du, S., Busch‐Nentwich, E. M., & Farber, S. A. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007105 · Cited by 106

Developments in RNA Splicing and Disease

Poulos, M. G., Batra, R., Charizanis, K., & Swanson, M. S. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000778 · Cited by 98

Genetics of Congenital Adrenal Hyperplasia

Hannah-Shmouni, F., Chen, W., & Merke, D. P. (2017) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2017.01.008 · Cited by 97

Increased Neuronal Excitability, Synaptic Plasticity, and Learning in Aged Kvβ1.1 Knockout Mice

Murphy, G. G., Fedorov, N. B., Giese, K.-P., Ohno, M., Friedman, E. L., Chen, R., & Silva, A. J. (2004) · Current Biology · doi:10.1016/j.cub.2004.10.021 · Cited by 94

Genotype–phenotype correlations in hereditary familial retinoblastoma

Taylor, M., Dehainault, C., Desjardins, L., Doz, F., Lévy, C., Sastre‐Garau, X., Couturier, J., Stoppa‐Lyonnet, D., Houdayer, C., & Gauthier‐Villars, M. (2006) · Human Mutation · doi:10.1002/humu.20443 · Cited by 91

Structure of the activated human minor spliceosome

Bai, R., Wan, R., Wang, L., Xu, K., Zhang, Q. C., Lei, J., & Shi, Y. (2021) · Science · doi:10.1126/science.abg0879 · Cited by 90

LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome

Fukuchi, K., Katsuya, T., Sugimoto, K., Kuremura, M., Kim, H. D., Li, L., & Ogihara, T. (2004) · Journal of Medical Genetics · doi:10.1136/jmg.2003.014688 · Cited by 82

The impact of alternative splicing in vivo: Mouse models show the way

Möröy, T., & Heyd, F. (2007) · RNA · doi:10.1261/rna.554607 · Cited by 80

Exon Silencing by UAGG Motifs in Response to Neuronal Excitation

An, P., & Grabowski, P. J. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050036 · Cited by 80

The splicing machinery is a genetic modifier of disease severity

Nissim‐Rafinia, M., & Kerem, B. (2005) · Trends in Genetics · doi:10.1016/j.tig.2005.07.005 · Cited by 81

Modifier genes and the plasticity of genetic networks in mice

Hamilton, B. A., & Yu, B. D. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002644 · Cited by 78

Restoration of the cystic fibrosis transmembrane conductance regulator function by splicing modulation

Nissim‐Rafinia, M., Aviram, M., Randell, S. H., Shushi, L., Ozeri, E., Chiba‐Falek, O., Eidelman, O., Pollard, H. B., Yankaskas, J. R., & Kerem, B. (2004) · EMBO Reports · doi:10.1038/sj.embor.7400273 · Cited by 71

FGF8 dose-dependent regulation of embryonic submandibular salivary gland morphogenesis

Jaskoll, T. F., Witcher, D., Toreno, L., Bringas, P., Moon, A., & Melnick, M. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.01.004 · Cited by 70

Urogenital and caudal dysgenesis in adrenocortical dysplasia ( acd ) mice is caused by a splicing mutation in a novel telomeric regulator

Keegan, C. E., Hutz, J. E., Else, T., Adamska, M., Shah, S. P., Kent, A. E., Howes, J. M., Beamer, W. G., & Hammer, G. D. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi011 · Cited by 68

Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions

Meisler, M. H., Plummer, N. W., Burgess, D. L., Buchner, D. A., & Sprunger, L. K. (2004) · Genetica · doi:10.1007/s10709-004-1441-9 · Cited by 67

Induced dystrophin exon skipping in human muscle explants

McClorey, G., Fall, A., Moulton, H. M., Iversen, P. L., Rasko, J. E. J., Ryan, M. M., Fletcher, S., & Wilton, S. D. (2006) · Neuromuscular Disorders · doi:10.1016/j.nmd.2006.05.017 · Cited by 66

Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice

Yang, Y. X., Mahaffey, C. L., Bérubé, N. G., Maddatu, T. P., Cox, G. A., & Frankel, W. N. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030124 · Cited by 64

Plant Cyclophilins: Multifaceted Proteins With Versatile Roles

Singh, H., Kaur, K., Singh, M., Kaur, G., & Singh, P. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.585212 · Cited by 63

Contrasting genetic architectures in different mouse reference populations used for studying complex traitsPreprint

Buchner, D. A., & Nadeau, J. H. (2015) · Genome Research · doi:10.1101/gr.187450.114 · Cited by 64

Design of a Bacterial Host for Site-Specific Incorporation of p-Bromophenylalanine into Recombinant Proteins

Kwon, I., Wang, P., & Tirrell, D. A. (2006) · Journal of the American Chemical Society · doi:10.1021/ja0626281 · Cited by 59

Deprivation of pantothenic acid elicits a movement disorder and azoospermia in a mouse model of pantothenate kinase‐associated neurodegeneration

Kuo, Y., Hayflick, S. J., & Gitschier, J. M. (2007) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-007-0560-8 · Cited by 59

Epileptogenic ion channel mutations: From bedside to bench and, hopefully, back again

Mantegazza, M., Rusconi, R., Scalmani, P., AVANZINI, G., & Franceschetti, S. (2010) · Epilepsy Research · doi:10.1016/j.eplepsyres.2010.08.003 · Cited by 59

Evolution of alternative splicing in primate brain transcriptomes

Lin, L., Shen, S., Jiang, P., Sato, S., Davidson, B. L., & Xing, Y. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq201 · Cited by 53

Rbfox proteins regulate alternative splicing of neuronal sodium channel SCN8A

O'Brien, J. E., Drews, V. L., Jones, J. M., Dugas, J. C., Barres, B. A., & Meisler, M. H. (2012) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.10.005 · Cited by 49

Bringing genetic background into focus

Chow, C. Y. (2015) · Nature Reviews Genetics · doi:10.1038/nrg.2015.9 · Cited by 48

The Genetic Incorporation of a Distance Probe into Proteins in Escherichia coli

Tsao, M., Summerer, D., Ryu, Y., & Schultz, P. G. (2006) · Journal of the American Chemical Society · doi:10.1021/ja058262u · Cited by 48

Genome-wide survey of allele-specific splicing in humans

Nembaware, V., Lupindo, B., Schouest, K. R., Spillane, C., Scheffler, K., & Seoighe, C. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-265 · Cited by 47

A Novel Mutation of COL2A1 Resulting in Dominantly Inherited Rhegmatogenous Retinal Detachment

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The genetics of health

Nadeau, J. H., & Topol, E. J. (2006) · Nature Genetics · doi:10.1038/ng1006-1095 · Cited by 47

Theataxia3Mutation in the N-Terminal Cytoplasmic Domain of Sodium Channel Nav1.6 Disrupts Intracellular Trafficking

Sharkey, L. M., Cheng, X., Drews, V. L., Buchner, D. A., Jones, J. M., Justice, M. J., Waxman, S. G., Dib‐Hajj, S. D., & Meisler, M. H. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6026-08.2009 · Cited by 45

Genetic modifiers of neurological disease

Kearney, J. A. (2011) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2010.12.007 · Cited by 43

Aberrant splicing in neurological diseases

Feng, D., & Xie, J. (2013) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1184 · Cited by 44

Evidence for a direct role of the disease modifier SCNM1 in splicing

Howell, V. M., Jones, J. M., Bergren, S. K., Li, L., Billi, A. C., Avenarius, M. R., & Meisler, M. H. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm206 · Cited by 41

The Primary Arrhythmia Syndromes: Same Mutation, Different Manifestations. Are We Starting to Understand Why?

Scicluna, B. P., Wilde, A. A. M., & Bezzina, C. R. (2008) · Journal of Cardiovascular Electrophysiology · doi:10.1111/j.1540-8167.2007.01073.x · Cited by 40

Mouse Models of PI(3,5)P2 Deficiency with Impaired Lysosome Function

Lenk, G. M., & Meisler, M. H. (2013) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-397926-1.00014-7 · Cited by 40

Voltage‐gated sodium channels: Action players with many faces

Koopmann, T. T., Bezzina, C. R., & Wilde, A. A. M. (2006) · Annals of Medicine · doi:10.1080/07853890600969072 · Cited by 40

Fine mapping of an epilepsy modifier gene on mouse Chromosome 19

Bergren, S. K., Rutter, E. D., & Kearney, J. A. (2009) · Mammalian Genome · doi:10.1007/s00335-009-9193-6 · Cited by 38

G lycine receptor mouse mutants: model systems for human hyperekplexia

Schaefer, N., Langlhofer, G., Kluck, C. J., & Villmann, C. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12335 · Cited by 37

A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses

Kim, J.-K., Jha, N. N., Awano, T., Caine, C., Gollapalli, K., Welby, E., Kim, S.-S., Fuentes, A., Wang, X., Feng, Z., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.004 · Cited by 37

Cerebellar ataxia and functional genomics: Identifying the routes to cerebellar neurodegeneration

Smeets, C. J. L. M., & Verbeek, D. S. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.04.004 · Cited by 36

Structural Characterization of a p-Acetylphenylalanyl Aminoacyl-tRNA Synthetase

Turner, J. M., Graziano, J. J., Spraggon, G., & Schultz, P. G. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0549042 · Cited by 34

An update on transcriptional and post-translational regulation of brain voltage-gated sodium channels

Onwuli, D. O., & Beltrán-Álvarez, P. (2015) · Amino Acids · doi:10.1007/s00726-015-2122-y · Cited by 33

Human voltage-gated Na + and K + channel properties underlie sustained fast AP signaling

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Multiple transcripts of sodium channel SCN8A (NaV1.6) with alternative 5′- and 3′-untranslated regions and initial characterization of the SCN8A promoter

Drews, V. L., Lieberman, A. P., & Meisler, M. H. (2004) · Genomics · doi:10.1016/j.ygeno.2004.09.002 · Cited by 31

Escaping from CRISPR–Cas-mediated knockout: the facts, mechanisms, and applications

Wang, Y., Zhai, Y., Zhang, M., Song, C., Zhang, Y., & Zhang, G. (2024) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-024-00565-x · Cited by 26

Enhanced VWF biosynthesis and elevated plasma VWF due to a natural variant in the murine Vwf gene

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Decreased locomotor activity in mice expressing tTA under control of the CaMKIIα promoter

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Nonsense-associated alternative splicing of T-cell receptor β genes: No evidence for frame dependence

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Alternative splicing induced by nonsense mutations in the immunoglobulin μ VDJ exon is independent of truncation of the open reading frame

Bühler, M., & Mühlemann, O. (2004) · RNA · doi:10.1261/rna.7183805 · Cited by 26

Modifiers of von Willebrand factor identified by natural variation in inbred strains of mice

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Asymmetric Synthesis and Translational Competence of l -α-(1-Cyclobutenyl)glycine

Jayathilaka, L. P., Deb, M., & Standaert, R. F. (2004) · Organic Letters · doi:10.1021/ol049026b · Cited by 24

Three ENU-induced neurological mutations in the pore loopof sodium channel Scn8a (Na v 1.6) and a genetically linkedretinal mutation, rd13

Buchner, D. A., Seburn, K. L., Frankel, W. N., & Meisler, M. H. (2004) · Mammalian Genome · doi:10.1007/s00335-004-2332-1 · Cited by 24

Ion Channels in Analgesia Research

Wood, J. N. (2007) · Springer eBooks · doi:10.1007/978-3-540-33823-9_12 · Cited by 23

Deletions within a CA-repeat-rich region of intron 4 of the human SP-B gene affect mRNA splicing

Lin, Z., Thomas, N. J., Wang, Y., Guo, X., Seifart, C., Shakoor, H., & Floros, J. (2005) · Biochemical Journal · doi:10.1042/bj20042032 · Cited by 22

A survey of splice variants of the human hypoxanthine phosphoribosyl transferase and DNA polymerase beta genes: products of alternative or aberrant splicing?

Skandalis, A. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh967 · Cited by 21

Genetic Modification of the Schisis Phenotype in a Mouse Model of X-Linked Retinoschisis

Johnson, B. A., Aoyama, N., Friedell, N. H., Ikeda, S., & Ikeda, A. (2008) · Genetics · doi:10.1534/genetics.107.084905 · Cited by 21

Common pathological mutations inPQBP1induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon

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Genetic modifiers in mice: the example of the fragile X mouse model

Errijgers, V., & Kooy, R. F. (2004) · Cytogenetic and Genome Research · doi:10.1159/000078218 · Cited by 19

Evidence in disease and non-disease contexts that nonsense mutations cause altered splicing via motif disruption

Abrahams, L., Savisaar, R., Mordstein, C., Young, B., Kudla, G., & Hurst, L. D. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab750 · Cited by 18

Identification of evolutionarily conserved, functional noncoding elements in the promoter region of the sodium channel gene SCN8A

Drews, V. L., Shi, K., de Haan, G., & Meisler, M. H. (2007) · Mammalian Genome · doi:10.1007/s00335-007-9059-8 · Cited by 18

Reduced Nav1.6 sodium channel activity in mice increases in vivo sensitivity to volatile anesthetics

Pal, D., Jones, J. M., Wisidagamage, S., Meisler, M. H., & Mashour, G. A. (2015) · PLOS ONE · doi:10.1371/journal.pone.0134960 · Cited by 17

Integrative Analysis of Nanopore and Illumina Sequencing Reveals Alternative Splicing Complexity in Pig Longissimus Dorsi Muscle

Shu, Z., Wang, L., Wang, J., Zhang, L., Hou, X., Yan, H., & Wang, L. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.877646 · Cited by 15

Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia

Iturrate, A., Rivera‐Barahona, A., Flores, C., Otaify, G. A., Elhossini, R. M., Pérez-Sanz, M. L., Nevado, J., Tenorio, J. A., Triviño, J. C., García-Gonzalo, F. R., et al. (2022) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2022.08.009 · Cited by 15

Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice

Alcaraz, W. A., Chen, E., Valdes, P., Kim, E., Lo, Y. H., Vo, J. A., & Hamilton, B. A. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr300 · Cited by 15

Relationship between Charge-Transfer Interactions, Redox Potentials, and Catalysis for Different Forms of the Flavoprotein Component ofp-Cresol Methylhydroxylase

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Serine–arginine-rich nuclear protein Luc7l regulates myogenesis in mice

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