Nuclear receptors: integration of multiple signalling pathways through phosphorylation

The nuclear receptor superfamily: the second decade

Mangelsdorf, D. J., Thummel, C., Beato, M., Herrlich, P., Schütz, G., Umesono, K., Blumberg, B., Kastner, P., Mark, M., Chambon, P., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90199-x · Cited by 6,964

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Cellular survival: a play in three Akts

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Mitogen-Activated Protein (MAP) Kinase Pathways: Regulation and Physiological Functions*

Pearson, G. W., Robinson, F. L., Gibson, T. B., Xu, B.-E., Karandikar, M. S., Berman, K. S., & Cobb, M. H. (2001) · Endocrine Reviews · doi:10.1210/edrv.22.2.0428 · Cited by 4,111

Oncogenic kinase signalling.

Blume-Jensen, P., & Hunter, T. (2001) · Nature · doi:10.1038/35077225 · Cited by 3,738

Molecular basis of agonism and antagonism in the oestrogen receptor

Brzozowski, A. M., Pike, A. C. W., Dauter, Z., Hubbard, R. E., Bonn, T., Engström, O., Öhman, L., Greene, G. L., Gustafsson, J.-Å., & Carlquist, M. (1997) · Nature · doi:10.1038/39645 · Cited by 3,355

Principles of CDK regulation

Morgan, D. O. (1995) · Nature · doi:10.1038/374131a0 · Cited by 3,288

A decade of molecular biology of retinoic acid receptors

Chambon, P. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.9.8801176 · Cited by 2,889

Ecdysone receptor and ultraspiracle proteins are tyrosine phosphorylated during adult development of silkmoths

Sridhara, S. (2011) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2011.11.001 · Cited by 10

Pin1 and Nuclear Receptors: A New Language?

Montagna, R. L., Caligiuri, I., Giordano, A., & Rizzolio, F. (2013) · Journal of Cellular Physiology · doi:10.1002/jcp.24316 · Cited by 10

Inhibition of the Androgen Receptor Activity by Coprinus comatus Substances

Dotan, N., Wasser, S. P., & Mahajna, J. A. (2011) · Nutrition and Cancer · doi:10.1080/01635581.2011.607542 · Cited by 10

Molecular Cross-Talk Between Nuclear Receptors and Nuclear Factor-κB

Beck, I. M. E., Haegeman, G., & Bosscher, K. D. (2010) · Springer eBooks · doi:10.1007/978-90-481-9531-2_10 · Cited by 9

PROTAC technology for prostate cancer treatment

Wang, Z., Zhang, D., Inuzuka, H., & Wei, W. (2025) · Acta Materia Medica · doi:10.15212/amm-2024-0075 · Cited by 9

MSK1 and Nuclear Receptors Signaling

Piskunov, A., & Rochette‐Egly, C. (2013) · Cited by 9

Correction: Smooth muscle 22 alpha protein inhibits VSMC foam cell formation by supporting normal LXRα signaling, ameliorating atherosclerosis

Zhang, D., Song, Y., Kong, P., Xu, X., Gao, Y., Dou, Y., Weng, L., Wang, X., Lin, Y.-L., Zhang, F., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04360-w · Cited by 9

Allosteric Regulation in the Ligand Binding Domain of Retinoic Acid Receptorγ

Chebaro, Y., Sirigu, S., Amal, I., Lutzing, R., Stote, R. H., Rochette-Egly, C., Rochel, N., & Dejaegere, A. (2017) · PLOS ONE · doi:10.1371/journal.pone.0171043 · Cited by 8

Type II nuclear receptors with potential role in Alzheimer disease

Muñoz-Cabrera, J., Adrián, S.-H., & Arboleda, G. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100940 · Cited by 9

Low-dose ethanol suppresses 17β-estradiol activity in GH4C1 pituitary tumor cells

Wang, G., Chen, D., Luo, H., Liu, J., Ji, X., Fan, J., & Cui, S. (2009) · Cell Biology and Toxicology · doi:10.1007/s10565-009-9129-7 · Cited by 7

Androgen receptor-mediated non-genomic effects of vinclozolin on porcine ovarian follicles and isolated granulosa cells

Wartalski, K., Knet, M., Hoja-Łukowicz, D., Tabarowski, Z., & Duda, M. (2016) · Acta Histochemica · doi:10.1016/j.acthis.2016.03.008 · Cited by 7

Roles of androgen-dependent and -independent activation of signal transduction pathways for cell proliferation of prostate cancer cells

Inoue, T., Kobayashi, T., Terada, N., Shimizu, Y., Kamoto, T., Ogawa, O., & Nakamura, E. (2007) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.2.5.689 · Cited by 9

Development of drugs against hormone‐refractory prostate cancer

Kageyama, Y. (2008) · Drug Development Research · doi:10.1002/ddr.20274 · Cited by 6

Platelet‐activating factor downregulates the expression of liver X receptor‐α and its target genes in human neutrophils

Reyes-Quiróz, M. E., Álba, G., Santa‐María, C., Coronilla, J. S., Geniz, I., Jiménez, J., Ramírez, R., Martín‐Nieto, J., Pintado, E., & Sobrino, F. (2013) · FEBS Journal · doi:10.1111/febs.12662 · Cited by 6

High Throughput Analysis of Nuclear Receptor–Cofactor Interactions

Goodson, M. L., Farboud, B., & Privalsky, M. L. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-575-0_9 · Cited by 6

Trichothiodystrophy

Stefanini, M. (2006) · Springer eBooks · doi:10.1007/0-387-36802-7_3 · Cited by 7

The intricate interplay between circadian rhythm, androgen signaling, hormone therapy, and cellular senescence in prostate cancer

Horestani, M. H., & Baniahmad, A. (2025) · Cancer and Metastasis Reviews · doi:10.1007/s10555-025-10302-1 · Cited by 5

Estrogen Receptor α/β–cofactor motif interactions; interplay of tyrosine 537/488 phosphorylation and LXXLL motifs

Nguyen, H. D., Phan, T. T. P., Carraz, M., & Brunsveld, L. (2012) · Molecular BioSystems · doi:10.1039/c2mb25257k · Cited by 5

Androgen Receptor

Modi, P. K., Faiena, I., & Kim, I. Y. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800077-9.00003-7 · Cited by 5

Coordinate regulation between the nuclear receptor peroxisome proliferator-activated receptor-γ and cyclooxygenase-2 in renal epithelial cells

Casali, C. I., Weber, K., Faggionato, D. M., Gómez, E. M., & Tome, M. C. F. (2014) · Biochemical Pharmacology · doi:10.1016/j.bcp.2014.06.002 · Cited by 5

Multifunnel Energy Landscapes for Phosphorylated Translation Repressor 4E-BP2 and Its Mutants

Kang, W., Jiang, F., Wu, Y., & Wales, D. J. (2019) · Journal of Chemical Theory and Computation · doi:10.1021/acs.jctc.9b01042 · Cited by 5

Effect of dietary palmitic and stearic acids on sucrose motivation and hypothalamic and striatal cell signals in the rat

Figlewicz, D. P., Jay, J. L., West, C. H., Zavosh, A., Hampe, C. S., Radtke, J. R., Raskind, M. A., & Peskind, E. R. (2017) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00340.2017 · Cited by 5

Expression, purification and characterization of methyl DNA binding protein from Bombyx mori

Uno, T., Nomura, Y., Nakamura, M., Nakao, A., Tajima, S., Kanamaru, K., Yamagata, H., & Iwanaga, Y. (2005) · Journal of Insect Science · doi:10.1673/031.005.0801 · Cited by 5

Role of HNF4α in the superinduction of the IL-1β-activated iNOS gene by oxidative stress

Gonzalez, F. J. (2006) · Biochemical Journal · doi:10.1042/bj20060005 · Cited by 5

The Nuclear Receptor Superfamily and Drug Discovery

Moore, J. T., Collins, J. L., & Pearce, K. H. (2007) · Chemical biology · doi:10.1002/9783527619375.ch15c · Cited by 5

The role of RARG in solid tumor progression and therapeutic potential

Guo, S., Han, H., Ding, B., Zhang, W., & Qin, L. (2026) · Discover Oncology · doi:10.1007/s12672-026-04706-w · Cited by 4

Production and characterization of a retinoic acid receptor RARγ construction encompassing the DNA binding domain and the disordered N-terminal proline rich domain

Martinez-Zapien, D., Delsuc, M., Travé, G., Lutzing, R., Rochette‐Egly, C., & Kieffer, B. (2013) · Protein Expression and Purification · doi:10.1016/j.pep.2013.12.001 · Cited by 4

Vitamin A Metabolism in the Fetus and Neonate

Ross, A. C., Tan, L., & Owusu, S. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00031-7 · Cited by 4

Down-regulation of estrogen receptor α (ERα) transcriptional activity by p27 is mediated by inhibition of ERα nuclear localization and modulation of the ERα transcriptional complex

Jeon, M. J., Yang, W., Seo, H.-S., Wang, E. S., & Shin, I. (2012) · Cellular Signalling · doi:10.1016/j.cellsig.2012.07.011 · Cited by 4

Prognostic and Therapeutic Potential of Nuclear Receptors in Head and Neck Squamous Cell Carcinomas

Knauer, S. K. (2009) · Journal of Oncology · doi:10.1155/2009/349205 · Cited by 4

Antifolate/folate-activated HGF/c-Met signalling pathways in mouse kidneys—the putative role of their downstream effectors in cross-talk with androgen receptor

Dudkowska, M., Bajer, S., Jaworski, T., Zielińska, J., Manteuffel-Cymborowska, M., & Grzelakowska-Sztabert, B. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.12.015 · Cited by 3

A Role for Acyclic Retinoid in the Chemoprevention of Hepatocellular Carcinoma: Therapeutic Strategy Targeting Phosphorylated Retinoid X Receptor-α

Sakai, H., Shimizu, M., & Moriwaki, H. (2014) · Diseases · doi:10.3390/diseases2030226 · Cited by 3

Nuclear Receptors

Taneja, R. (2005) · Science s STKE · doi:10.1126/stke.2862005tr17 · Cited by 3

Protein Posttranslational Modification: A Potential Target in Pharmaceutical Development

Huq, M. D. M., & Wei, L. (2010) · Pharmaceutical Sciences Encyclopedia · doi:10.1002/9780470571224.pse302 · Cited by 3

RARG promotes gastric cancer progression by activating PMEPA1 transcription and Wnt/β-catenin signalling

Qin, L., Wen, F., Guo, S., Zhang, W., Cai, W., Ma, R., Liu, C., Ren, W., Ye, H., & Jiao, Z. (2026) · Cellular Signalling · doi:10.1016/j.cellsig.2026.112552 · Cited by 2

Regulation of Bone Cell Function by Estrogens

Komm, B. S., Cheskis, B. J., & Bodine, P. V. N. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-375098-3.50015-9 · Cited by 2

Functions of the Liver

Renato, P., Correa, A. V., Nathanson, M. H., Wolkoff, A. W., Novikoff, P. M., Thevananther, S., Karpen, S. J., Elferink, R. P. J. O., Püschel, G. P., & Stieger, B. (2007) · Wiley eBooks · doi:10.1002/9780470691861.ch2b · Cited by 3

Estrogen receptors and anti-estrogen therapies.

Buluwela, L., Constantinidou, D., Pike, J., & Ali, S. (2004) · Cancer treatment and research · doi:10.1007/1-4020-7847-1_13 · Cited by 2

The Role of Cyclic AMP in Regulating the Androgen Receptor

Sadar, M. D. (2009) · Springer eBooks · doi:10.1007/978-0-387-69179-4_21 · Cited by 1

Novel Approaches to Androgen Receptor Blockade

Mellinghoff, I. K. (2006) · Translational medicine series · doi:10.3109/9781420019858.010 · Cited by 1

Endocrine Active Compounds Actions during Neonatal Period: Effect on the Ovary

Słomczyńska, M., Grzesiak, M., & Knapczyk‐Stwora, K. (2018) · InTech eBooks · doi:10.5772/intechopen.69220 · Cited by 1

Chemical and Drug Receptor Interactions

Konsoula, Z. (2010) · CRC Press eBooks · doi:10.3109/9781420092264-12 · Cited by 1

The Role of Androgens in Ovarian Follicular Development: From Fertility to Ovarian Cancer

Duda, M., Wartalski, K., Tabarowski, Z., & Gorczyca, G. (2017) · InTech eBooks · doi:10.5772/intechopen.68881 · Cited by 1

Nuclear Receptors

Kramer, I. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394803-8.00008-5 · Cited by 1

Control of Gene Expression by Nuclear Retinoic Acid Receptors

Carrier, M., & Rochette‐Egly, C. (2015) · doi:10.1002/9781118628003.ch5 · Cited by 1

Prostate Cancer: Role of Vav3 Overexpression in Development and Progression

Lu, S. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8442-3_31 · Cited by 1

Androgen Receptor Coregulators and Their Role in Prostate Cancer

Wafa, L. A., Snoek, R., & Rennie, P. S. (2009) · Springer eBooks · doi:10.1007/978-0-387-69179-4_15 · Cited by 1

Nuclear Receptors

Bolander, F. F. (2004) · Elsevier eBooks · doi:10.1016/b978-012111232-5/50006-3 · Cited by 1

CHAPTER 14 – Regulation of Bone Cell Function by Estrogens

Komm, B., Cheskis, B., & Bodine, P. (2008) · Elsevier eBooks · doi:10.1016/b978-012370544-0.50016-1

Etude de DAX-1 et de sa perte de fonction dans l'hypoplasie congénitale des glandes surrénales

Lehmann, S. (2005) · OpenGrey (Institut de l'Information Scientifique et Technique)

Receptores de hormônios da tireóide: estudos computacionais, ressonância plasmônica de superfície e ensaios celulares

Valadares, N. F. (2008) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.76.2008.tde-18122008-154730

Transcriptional regulation by the orphan nuclear receptor ERRgamma

Hirvonen, J. (2008) · Työväentutkimus Vuosikirja

Studies on the function of the NGFIC subfamily of nuclear receptors in adipose tissue.

Wakes, N. C. (2006) · UCL Discovery (University College London)

Regulation of Estrogen Receptor alpha Ubiquitination and Proteasome-mediated Receptor Degradation

Berry, N. B. (2008) · IUScholarWorks (Indiana University)

Application of Different Bioanalytical Workflows for Proteomics of Prostate Cancer

Chen, L. (2009) · doi:10.21007/etd.cghs.2009.0050

Molecular Dynamic Studies of Nuclear Receptors Ligand Binding Domain

Burendahl, S. (2009) · Figshare

Signalling Pathways and Gene Expression Profiles in Prostate Cancer

Hatziieremia, S., McCall, P., & Edwards, J. (2011) · InTech eBooks · doi:10.5772/26971

Retinoid-induced apoptosis and proliferation of hepatocytes are mediated by distinct nuclear receptors

Bu, P. (2009) · KU ScholarWorks (The University of Kansas)

The production and purification of functional steroid hormone receptor ligand binding domains towards the development of a biological endocrine disruptor detection system

Tait, T. (2015) · SUNScholar (Stellenbosch University)

Nuclear receptor and cofactor expression in female reproductive tissues

Vienonen, A. (2004) · Tampere University Institutional Repository (Tampere University)

MOLECULAR DETERMINANTS OF ANDROGEN ACTION

Santti, H. (2004) · Työväentutkimus Vuosikirja

Inhibition of castration resistant prostate cancer by sintokamide A : an antagonist of the amino-terminus of the androgen receptor

Tavakoli, I. (2013) · cIRcle (University of British Columbia) · doi:10.14288/1.0072850

Cushing's syndrome results from lengthy and inappropriate exposure to excessive glucocorticoids. Untreated, it has signifi cant morbidity and mortality. The syndrome remains a challenge to diagnose and manage. Here, we review the current understanding of pathogenesis, clinical features, diagnostic, and diff erential diagnostic approaches. We provide diagnostic algorithms and recommendations for management.

Newell-Price, J. D. C., BERTAGNA, X. Y., Grossman, A. B., & Nieman, L. K. (2006)

All-trans retinoic acid downregulates CCAAT/ enhancer binding proteins in human bronchial epithelial cells

Aldhamen, Y. A. (2007) · OhioLink ETD Center (Ohio Library and Information Network)

Retinoic Acid Receptors

Cras, A., Guidez, F., & Chomienne, C. (2010) · Springer eBooks · doi:10.1007/978-90-481-3303-1_9

The Role of EGFR, HER 2-4, Heregulin and Downstream Signalling in Prostate Adenocarcinoma

Grimsley, S. J. S. (2008) · Enlighten: Theses (The University of Glasgow)

Activation of the Retinoid X Receptor Augments the Expression of Akt2 to Enhance Myogenic Differentiation

AlSudais, H. (2015) · uO Research (University of Ottawa) · doi:10.20381/ruor-4024

Identification in silico d’éléments de réponse de récepteurs nucléaires impliqués dans le cancer du sein

Laperrière, D. (2008) · doi:10.71781/25843

Mammalian Mat1 subunit of Transcription Factor IIH in gene-specific and general transcription

Helenius, K. (2011) · Työväentutkimus Vuosikirja

A new feature of CK2 function: it's role in granulocytic differentiation induced by retinoic acid

Tubi, L. Q. (2012)

PPM1A Phosphatase is Involved in Regulating Pregnane Xenobiotic Receptor Mediated Cytochrome P450 3A4 Gene Expression

Flannery, P. C. (2014)

Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties

Carnahan, V. E. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/346x-vf17

Chemical– and Drug–Receptor Interactions

Konsoula, Z. (2019) · CRC Press eBooks · doi:10.1201/9780429154829-11

A brief overview of androgen receptor: Its structure, functions and role in health and disease

Nikhil, K., Sharan, S., & Roy, P. (2013) · Journal of Endocrinology & Reproduction · doi:10.18519/jer/2013/v17/75783

Studies on the promiscuous xenobiotic receptor (PXR, NR1I2) in zebrafish: antibody characterisation and genetic variation in zebrafish embryos

Hitchcock, D. J. (2014) · NORA - Norwegian Open Research Archives

Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells

Chen, C. (2016) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)

14-3-3 sigma interacts with liver X receptor beta

Jackson, E. A. (2010) · Louisiana State University · doi:10.31390/gradschool_theses.4251

The Effect of DHT Treatment on Changes in Amino Acid Transport Occurring in Aged Muscle

Wendowski, O. (2018) · UEA Digital Repository (University of East Anglia)

Analyse structurale et fonctionnelle du récepteur nucléaire orphelin NOR-1 et inactivation du gène chez la souris

Maltais, A. (2006) · Corpus Université Laval (Université Laval)

Role of peroxisome proliferator-activated receptors in the control of alcohol dependence and concomitant liver pathology

Semenenya, I. N., Shlyahtun, A. H., & Радута, Е. Ф. (2019) · Proceedings of the National Academy of Sciences of Belarus Medical series · doi:10.29235/1814-6023-2019-16-2-244-256

Nuclear Receptors

Gomperts, B. D., Kramer, I. M., & Tatham, P. E. R. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-369441-6.00010-6

RXR – centralny regulator wielu ścieżek sygnałowych w organizmie

Sołtys, K., Leszczyński, B., & Ożyhar, A. (2021) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.2478/ahem-2021-0005

Prédiction de boucles de régulation associant microARN et gènes régulés par le récepteur de l'acide rétinoïque dans le cancer du sein

Boufaden, A. (2011) · doi:10.71781/30526

Regulation of the Pregnane X Receptor Signaling Pathway

Lichti-Kaiser, K. (2009) · KU ScholarWorks (University of Kansas)

Data from Targeted Overexpression of Vav3 Oncogene in Prostatic Epithelium Induces Nonbacterial Prostatitis and Prostate Cancer

Liu, Y., Mo, J. Q., Hu, Q., Boivin, G. P., Levin, L. S., Lu, S., Yang, D., & Dong, Z. (2023) · doi:10.1158/0008-5472.c.6498122

Data from Targeted Overexpression of Vav3 Oncogene in Prostatic Epithelium Induces Nonbacterial Prostatitis and Prostate Cancer

Liu, Y., Mo, J. Q., Hu, Q., Boivin, G. P., Levin, L. S., Lu, S., Yang, D., & Dong, Z. (2023) · doi:10.1158/0008-5472.c.6498122.v1

Effets des ligands de PPAR? sur la voie de signalisation des oestrogènes dans les cellules cancéreuses mammaires

Lecomte, J. (2009) · theses.fr (ABES) · doi:10.70675/5c85b2d6z8af3z49beza96dz381f1cb9fa4c

Evolution of Steroid Signaling in Metazoans

Markov, G. V. (2011) · theses.fr (ABES) · doi:10.70675/816a1939zc7e3z4c7azb90fzf9d9a08011af

Role of PGC-1β and TIF2 co-regulators in mouse skeletal muscle function

Ramamoorthy, T. G. (2013) · theses.fr (ABES) · doi:10.70675/e05002c4z4806z4363z90b1z0e406b6c0e4c

Role of PPARγ in human placental development and pregnancy outcome : impact of phthalates and of the PPARγ mutation (E352Q) on trophoblast differentiation

Shoaito, H. (2019) · doi:10.70675/5009d482z4b2cz45e6zb1b2ze17f98a5237d

Multiple regulators mediate the transcriptional activities of ERRalpha and its capacity to promote cell invasion

Zhang, L. (2018) · theses.fr (ABES) · doi:10.70675/81bc582az881bz4821zb118z528d958af63d

Hyodeoxycholic acid rejuvenates BMSCs against postmenopausal osteoporosis by attenuating senescence and aberrant adipogenesis via TGR5-ESR1-mediated mitophagy

Zeng, C., Wenhui, Y., Kang, Y., Liu, W., Chen, Z., Xiao, Z., Liu, Z., Zhang, W., Li, Q., Zeng, Y., et al. (2026) · Journal of Advanced Research · doi:10.1016/j.jare.2026.10.020

Phosphorylation Control of Nuclear Receptors

Lalevée, S., Ferry, C., & Rochette‐Egly, C. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-738-9_15 · Cited by 24

Phosphorylation of nuclear receptors: Novelty and therapeutic implications

Shindo, S., Kakizaki, S., Sakaki, T., Kawasaki, Y., Sakuma, T., Negishi, M., & Shizu, R. (2023) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108477 · Cited by 14

Transcriptional Regulation by Steroid Receptor Coactivator Phosphorylation

Wu, R., Smith, C. L., & O’Malley, B. W. (2005) · Endocrine Reviews · doi:10.1210/er.2004-0018 · Cited by 155

Nuclear Receptors: Nomenclature, Ligands, Mechanisms of Their Effects on Gene Expression

Smirnov, A. N. (2002) · Biochemistry (Moscow) · doi:10.1023/a:1020545200302 · Cited by 62

The Putative Cofactor TIF1α Is a Protein Kinase That Is Hyperphosphorylated upon Interaction with Liganded Nuclear Receptors

Fraser, R., Heard, D. J., Adam, S., Lavigne, A.-C., Douarin, B. L., Tora, L., Losson, R., Rochette‐Egly, C., & Chambon, P. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.26.16199 · Cited by 68