Metabolic Pitfalls of CNS Cre-Based Technology

A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

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Generalized lacZ expression with the ROSA26 Cre reporter strain

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Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety

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Rapid, reversible activation of AgRP neurons drives feeding behavior in mice

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Genetic transformation of mouse embryos by microinjection of purified DNA.

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Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies

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Remote Control of Neuronal Activity in Transgenic Mice Expressing Evolved G Protein-Coupled Receptors

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Hypoxia-Inducible Factor 1α Induces Fibrosis and Insulin Resistance in White Adipose Tissue

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Talking about a Revolution

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Bacteriophage P1 site-specific recombination

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Decreased adipogenesis and adipose tissue in mice with inactivated protein phosphatase 5

Jacob, W., Rosenzweig, D., Vázquez‐Martin, C., Duce, S., & Cohen, P. T. W. (2014) · Biochemical Journal · doi:10.1042/bj20140428 · Cited by 17

Sex-specific brain erythropoietin regulation of mouse metabolism and hypothalamic inflammation

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Molecular targets for endogenous glial cell line-derived neurotrophic factor modulation in striatal parvalbumin interneurons

Enterría‐Morales, D., del Rey, N. L., Blesa, J., López‐López, I., Gallet, S., Prévot, V., López‐Barneo, J., & de Tassigny, X. D. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa105 · Cited by 17

CACNA1C gene regulates behavioral strategies in operant rule learning

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DEPTOR in POMC neurons affects liver metabolism but is dispensable for the regulation of energy balance

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The SWI/SNF subunit Bcl7a contributes to motor coordination and Purkinje cell function

Wischhof, L., Maida, S., Piazzesi, A., Gioran, A., Sanz, K. B., Irsen, S. H., Beyer, M., Schultze, J. L., Dyer, M. J. S., Salomoni, P., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-17284-3 · Cited by 16

Brain-Body Control of Glucose Homeostasis—Insights From Model Organisms

MacDonald, A. J., Yang, Y. H. C., Cruz, A. M., Beall, C., & Ellacott, K. L. J. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.662769 · Cited by 16

The Antipsychotic Dopamine 2 Receptor Antagonist Diphenylbutylpiperidines Improve Glycemia in Experimental Obesity by Inhibiting Succinyl-CoA:3-Ketoacid CoA Transferase

Dakhili, S. A. T., Greenwell, A. A., Yang, K., Farraj, R. A., Saed, C. T., Gopal, K., Chan, J. S. F., Chahade, J. J., Eaton, F., Lee, C., et al. (2022) · Diabetes · doi:10.2337/db22-0221 · Cited by 16

Serine Racemase mediates subventricular zone neurogenesis via fatty acid metabolism

Roychaudhuri, R., Atashi, H., & Snyder, S. H. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.05.015 · Cited by 15

TAK1 determines susceptibility to endoplasmic reticulum stress and leptin resistance in the hypothalamus

Sai, K., Morioka, S., Takaesu, G., Muthusamy, N., Ghashghaei, H. T., Hanafusa, H., Matsumoto, K., & Ninomiya‐Tsuji, J. (2016) · Journal of Cell Science · doi:10.1242/jcs.180505 · Cited by 15

Differential CRE Expression in Lhrh-cre and GnRH-cre Alleles and the Impact on Fertility in Otx2-Flox Mice

Hoffmann, H. M., Larder, R., Lee, J. S., Hu, R. J., Trang, C., Devries, B. M., Clark, D. D., & Mellon, P. L. (2019) · Neuroendocrinology · doi:10.1159/000497791 · Cited by 15

Single-Base Pair Genome Editing in Human Cells by Using Site-Specific Endonucleases

Ochiai, H. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160921128 · Cited by 15

Neuronal loss of TRPM8 leads to obesity and glucose intolerance in male mice

Liśkiewicz, D., Zhang, Q., Barthem, C. S., Jastroch, M., Liśkiewicz, A., Khajavi, N., Grandl, G., Coupland, C. A. C., Kleinert, M., García‐Cáceres, C., et al. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101714 · Cited by 14

A detrimental role of RelB in mature oligodendrocytes during experimental acute encephalomyelitis

Gupta, A. S., Biswas, D. D., Brown, L. N., Mockenhaupt, K., Marone, M. G., Hoskins, A., Siebenlist, U. K., & Kordula, T. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1548-7 · Cited by 16

Early-onset Purkinje cell dysfunction underlies cerebellar ataxia in peroxisomal multifunctional protein-2 deficiency

Munter, S. D., Verheijden, S., Vanderstuyft, E., Malheiro, A. R., Brites, P., Gall, D., Schiffmann, S. N., & Baes, M. I. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.06.012 · Cited by 14

mtDNA leakage promotes neuron–glia crosstalk to induce epilepsy by cGAS–STING-driven neuroinflammation and serine metabolic reprogramming

Jiang, J., Zuo, M., Zhao, K., Ling, Z., Wu, Z., Xue, D., Mo, S., Liu, Y., Chen, Y., Wang, J., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2522313123 · Cited by 14

The role of growth hormone receptor in β cell function

Wang, S., Wu, J. C., Wang, N., Zeng, L., & Wu, Y. (2017) · Growth Hormone & IGF Research · doi:10.1016/j.ghir.2017.08.002 · Cited by 13

Growth hormone receptor contributes to the activation of STAT5 in the hypothalamus of pregnant mice

Wasinski, F., Teixeira, P. D. S., List, E. O., Kopchick, J. J., & Donato, J. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136402 · Cited by 12

Exploring germline recombination in Nestin‐Cre transgenic mice using floxed androgen receptor

McLeod, V. M., Cuic, B., Chiam, M. D. F., Lau, C. L., & Turner, B. J. (2020) · genesis · doi:10.1002/dvg.23390 · Cited by 12

Mouse Insulin Cells Expressing an Inducible RIPCre Transgene Are Functionally Impaired

Teitelman, G., & Kedees, M. H. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.615484 · Cited by 13

How technical progress reshaped behavioral neuroendocrinology during the last 50 years… and some methodological remarks

Balthazart, J. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104682 · Cited by 8

Screening strategy to generate cell specific recombination: a case report with the RIP-Cre mice

Spinelli, V., Martin, C., Dorchies, E., Vallez, E., Dehondt, H., Trabelsi, M.-S., Tailleux, A., Caron, S., & Staels, B. (2015) · Transgenic Research · doi:10.1007/s11248-015-9889-1 · Cited by 12

TIA1-mediated stress granules promote neurodegeneration by sequestering HSP70 mRNA in C9orf72 mice

Wei, Y., Li, D., Yang, R., Liu, Y., Luo, X., Zhao, W., Yang, H., Chen, Z., Shen, C., Wang, Y., et al. (2025) · Brain · doi:10.1093/brain/awaf248 · Cited by 11

Hypothalamic NUCKS regulates peripheral glucose homoeostasis

Qiu, B., Shi, X., Zhou, Q., Chen, H. S., Lim, J., Han, W., & Tergaonkar, V. (2015) · Biochemical Journal · doi:10.1042/bj20150450 · Cited by 11

Synaptotagmin 2 is ectopically overexpressed in excitatory presynapses of a widely used CaMKΙΙα-Cre mouse line

Matsuura, K., Mohamed, H. M. A., Youssef, M., Yoshida, Y., & Yamamoto, T. S. (2022) · iScience · doi:10.1016/j.isci.2022.104692 · Cited by 10

Insulin Does Not Target Camk II α Neurones to Critically Regulate the Neuroendocrine Reproductive Axis in Mice

Evans, M. C., Rizwan, M. Z., & Anderson, G. M. (2015) · Journal of Neuroendocrinology · doi:10.1111/jne.12330 · Cited by 10

Microsomal triglyceride transfer protein contributes to lipid droplet maturation in adipocytes

Swift, L. L., Love, J. D., Harris, C. M., Chang, B. H., & Jerome, W. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181046 · Cited by 11

Leptin Receptors in RIP-Cre25Mgn Neurons Mediate Anti-dyslipidemia Effects of Leptin in Insulin-Deficient Mice

Singha, A. K., Palavicini, J. P., Pan, M., Farmer, S., Sandoval, D. A., Han, X., & Fujikawa, T. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.588447 · Cited by 10

Cre Recombinase

Duyne, G. D. V. (2015) · ASM Press eBooks · doi:10.1128/9781555819217.ch5 · Cited by 10

Igf1R/InsR function is required for axon extension and corpus callosum formation

Jin, J., Ravindran, P., Meo, D. D., & Püschel, A. W. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219362 · Cited by 11

Dissociation of disease onset, progression and sex differences from androgen receptor levels in a mouse model of amyotrophic lateral sclerosis

Tomas, D., McLeod, V. M., Chiam, M. D. F., Wanniarachchillage, N., Boon, W. C., & Turner, B. J. (2021) · Scientific Reports · doi:10.1038/s41598-021-88415-0 · Cited by 9

Aberrant glial activation and synaptic defects in CaMKIIα-iCre and nestin-Cre transgenic mouse models

Alia, A. O., Jeon, S., Popović, J., Salvo, M. A., Sadleir, K. R., Vassar, R. J., & Cuddy, L. K. (2022) · Scientific Reports · doi:10.1038/s41598-022-26671-4 · Cited by 9

Sex-specific effects of Cre expression in Syn1Cre mice

Baghdadi, M., Mesaros, A., Purrio, M., & Partridge, L. (2023) · Scientific Reports · doi:10.1038/s41598-023-37029-9 · Cited by 9

Neuronal Cell Adhesion Molecule 1 Regulates Leptin Sensitivity and Bone Mass

Yan, X., Kononenko, N. L., Brüel, A., Thomsen, J. S., & Poy, M. N. (2017) · Calcified Tissue International · doi:10.1007/s00223-017-0361-5 · Cited by 9

Brain-specific natriuretic peptide receptor-B deletion attenuates high-fat diet-induced visceral and hepatic lipid deposition in mice

Yamashita, Y., Yamada-Goto, N., Katsuura, G., Ochi, Y., Kanai, Y., Miyazaki, Y., Kuwahara, K., Kanamoto, N., Miura, M., Yasoda, A., et al. (2016) · Peptides · doi:10.1016/j.peptides.2016.03.014 · Cited by 8

Modeling Cancer Using Genetically Engineered Mice

Stiedl, P., Grabner, B., Zboray, K., Bogner, E., & Casanova, E. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2297-0_1 · Cited by 8

PGC-1β-expressing POMC neurons mediate the effect of leptin on thermoregulation in the mouse

Delezie, J., Gill, J. F., Santos, G., Karrer‐Cardel, B., & Handschin, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-73794-7 · Cited by 9

Sodium appetite and thirst do not require angiotensinogen production in astrocytes or hepatocytes

Peltekian, L., Gasparini, S., Fazan, F. S., Karthik, S., Iverson, G. N., Resch, J. M., & Geerling, J. C. (2023) · The Journal of Physiology · doi:10.1113/jp283169 · Cited by 8

Realities and Misconceptions on the Pericytes Role in Tissue Repair

Campagnolo, P., Katare, R., & Madeddu, P. R. (2018) · Regenerative Medicine · doi:10.2217/rme-2017-0091 · Cited by 8

Misprogramming of glucose metabolism impairs recovery of hippocampal slices from neuronal GLT‐1 knockout mice and contributes to excitotoxic injury through mitochondrial superoxide production

Li, S., Wang, J., Andersen, J. V., Aldana, B. I., Zhang, B. X., Prochownik, E. V., & Rosenberg, P. A. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16205 · Cited by 7

Central deficiency of IL-6Ra in mice impairs glucose-stimulated insulin secretion

McNeilly, A. D., Yiannakas, A., Gallagher, J. G., Tarlton, J., Ashford, M. L. J., & McCrimmon, R. J. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101488 · Cited by 7

An optimized protocol for the generation and monitoring of conditional orthotopic lung cancer in the KP mouse model using an adeno-associated virus vector compatible with biosafety level 1

Deng, H., Ge, H., Dubey, C., Losmanová, T., Medová, M., Konstantinidou, G., Mutlu, S. M., Birrer, F., Brodie, T. M., Stroka, D., et al. (2023) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-023-03542-z · Cited by 7

Characterization of social behavior in young and middle-aged ChAT-IRES-Cre mouse

Lhopitallier, C., Perrault, C., Chauveau, F., Saurini, F., Berrard, S., Granon, S., & Faure, A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0272141 · Cited by 7

Embryonic ablation of neuronal VGF increases energy expenditure and reduces body weight

Jiang, C. S., Lin, W., Sadahiro, M., Shin, A. C., Buettner, C., & Salton, S. R. (2016) · Neuropeptides · doi:10.1016/j.npep.2016.12.005 · Cited by 7

Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons

Furigo, I. C., Teixeira, P. D., de, S. G. O., Couto, G. C. L., Romero, G. G., Perelló, M., Frazão, R., Elias, L. L. K., Metzger, M., List, E. O., et al. (2019) · Yearbook of pediatric endocrinology · doi:10.1530/ey.16.15.10 · Cited by 6

High frequency of germline recombination in Nestin-Cre transgenic mice crossed with Glucagon-like peptide 1 receptor floxed mice

Kajitani, Y., Miyazawa, T., Inoue, T., Kajitani, N., Fujita, M., Takeichi, Y., Miyachi, Y., Sakamoto, R., & Ogawa, Y. (2023) · PLoS ONE · doi:10.1371/journal.pone.0296006 · Cited by 5

Developmental or adult-onset deletion of neurotensin receptor-1 from dopamine neurons differentially reduces body weight

Perez‐Bonilla, P., Ramirez‐Virella, J., Menon, P., Troyano‐Rodriguez, E., Arriaga, S. K., Makela, A. G., Bugescu, R., Beckstead, M. J., & Leinninger, G. M. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.874316 · Cited by 5

Application of a split‐Cre system for high‐capacity adenoviral vector amplification

González-Aparicio, M., Buñuales, M., de Landazuri, I. O., Prìeto, J., & Hernández-Alcoceba, R. (2022) · Biotechnology Journal · doi:10.1002/biot.202200227 · Cited by 5

Toward dissection of diverse neural components in the suprachiasmatic nucleus (SCN) pacemaker network

Izumo, M., Cox, K. H., & Takahashi, J. S. (2026) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2026.100143 · Cited by 5

Uncovering the role of Gpr45 in obesity regulation

Karolczak, E. O., Li, C., Alcantara, I. C., Cohen, I. M., Gao, C., Xiao, C., Goldschmidt, A. I., Pinkus, C. A., Li, J., Li, M. M., et al. (2025) · Molecular Metabolism · doi:10.1016/j.molmet.2025.102174 · Cited by 4

Assessing leaky expression of Cre-dependent DNA constructs in the mouse genome using sensitive bioluminescent reporters

Nakashiba, T., Sugiyama, T., Iwano, S., Iwama, M., Yoshiki, A., Miyawaki, A., & Abe, K. (2026) · Cell Reports Methods · doi:10.1016/j.crmeth.2026.101369 · Cited by 4

Estrogen Receptor-α Knockout Mice

Antonson, P., Humire, P., & Gustafsson, J.-Α. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-3127-9_33 · Cited by 4

Brain-specific PAPP-A knock-out mice?

Bale, L. K., West, S. A., & Conover, C. A. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111548 · Cited by 4

Embryonic and early postnatal cranial bone volume and tissue mineral density values for C57BL / 6J laboratory mice

Lesciotto, K. M., Tomlinson, L., Leonard, S., & Richtsmeier, J. T. (2022) · Developmental Dynamics · doi:10.1002/dvdy.458 · Cited by 4

Neuron-specific Mafb knockout causes growth retardation accompanied by an impaired growth hormone/insulin-like growth factor I axis

Maimaiti, S., Koshida, R., Ojima, M., Kulathunga, K., Oishi, H., & Takahashi, S. (2019) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.18-0182 · Cited by 4

A conditional Pax6 depletion study with no morphological effect on the adult mouse corneal epithelium

Dorà, N. J., Manuel, M. N., Kleinjan, D., Price, D. J., Collinson, J. M., Hill, R. E., & West, J. D. (2018) · BMC Research Notes · doi:10.1186/s13104-018-3812-9 · Cited by 4

Ganglioside deficiency in hypothalamic POMC neurons promotes body weight gain

Dieterle, V., Herzer, S., Gröne, H., Jennemann, R., & Nordström, V. (2019) · International Journal of Obesity · doi:10.1038/s41366-019-0388-y · Cited by 4

Neuronal differentiation reporter mice as a new methodology for detecting in vivo developmental neurotoxicity

Ishida, K., Tatsumi, K., Minamigawa, Y., Mori, K., Matsumaru, D., Nagase, H., Kanda, Y., Takuma, K., & Nakanishi, T. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115332 · Cited by 3

CRMP2 conditional knockout changes axonal function and ultrastructure of axons in mice corpus callosum

Grycel, K., Larsen, N. Y., Feng, Y., Qvortrup, K., Jensen, P. H., Fayyaz, M., Madsen, M. G., Midtgaard, J., Xu, Z., Hasselholt, S., et al. (2023) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2023.103882 · Cited by 3

The caveats and setbacks of mouse genome editing tools in biomedical studies

Li, A. H., & Yang, S. (2023) · Gene Reports · doi:10.1016/j.genrep.2023.101834 · Cited by 3

Fas ( CD95 ) expression in adipocytes contributes to diet‐induced obesity

Wueest, S., Scaffidi, C., van Krieken, P. P., Konrad, N. K., Koch, C., Wiedemann, M. S. F., Goergen, A., Borsigova, M., Lempesis, I. G., Fullin, J., et al. (2024) · Obesity · doi:10.1002/oby.24092 · Cited by 4

Current Genetic Techniques in Neural Circuit Control of Feeding and Energy Metabolism

Wu, Q., Han, Y., & Tong, Q. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1286-1_12 · Cited by 3

Human Growth Hormone in Transgenesis: A Growing Problem?

Brouwers, B., & Creemers, J. W. M. (2015) · Diabetes · doi:10.2337/dbi15-0007 · Cited by 3

Unexpected Phenotypes in Mouse Models Carrying the Human Growth Hormone Minigene to Enhance Transgene Expression

Brouwers, B. (2015) · Journal of Steroids & Hormonal Science · doi:10.4172/2157-7536.1000.e115 · Cited by 2

A novel mutation in Slc2a4 as a mouse model of fatigue

de Groot, M. H. M., Castorena, C. M., Cox, K. H., Kumar, V., Mohawk, J. A., Ahmed, N. I., & Takahashi, J. S. (2019) · Genes Brain & Behavior · doi:10.1111/gbb.12578 · Cited by 2

Systemic Glucose Homeostasis Requires Pancreatic but Not Neuronal ATP-sensitive Potassium Channels

Li, A. H., Tsai, W.-S., Tsai, W.-H., & Yang, S. (2025) · Function · doi:10.1093/function/zqaf002 · Cited by 2

Neuropeptide Neuromedin B does not alter body weight and glucose homeostasis nor does it act as an insulin-releasing peptide

Cikes, D., Atanes, P., Cronin, S. J. F., Hagelkrüys, A., Huang, G.-C., Persaud, S. J., & Penninger, J. M. (2022) · Scientific Reports · doi:10.1038/s41598-022-13060-0 · Cited by 2

Role of intestinal claudin-2 in calcium permeability and whole body calcium balance

Nyimanu, D., Behm, C. V., & Yu, A. S. L. (2025) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00133.2025 · Cited by 1

Prodromal changes in cortical neuron physiology before amyloid pathology in a mild model of Alzheimer’s disease

Milicevic, K. D., Abreu, A. C., Chandran, G., Zhu, Y. M. D., Hu, X., Ivanova, V. O., Jami, M., Simon, B., Fernández, I., Yan, R., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-47370-4 · Cited by 1

Loss of Echs1 in neural stem and progenitor cells impairs neurogenesis via ER stress activation and lipid metabolic reprogramming

Duan, C.-H., Liu, P., Sun, X. X., Ma, W.-H., Pang, J.-Y., ZHANG, Z., Li, X. Z., Jiao, L., Du, H., Teng, Z., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-75063-z · Cited by 1

Pancreatic ductal cell antigens are important in the development of invasive insulitis in Non-Obese Diabetic mice

Jayasimhan, A., Ellis, D., Ziegler, A. I., & Slattery, R. M. (2019) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2019.01.001 · Cited by 1

Autophagy in adipose tissue

Vinod, V., & Boudina, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822003-0.00018-8 · Cited by 1

Problems with Technologies of Genomic Editing and Transgenesis

Bolshakov, A. P. (2021) · Neurochemical Journal · doi:10.1134/s1819712421040036 · Cited by 1

Hypothalamic Nutrient Sensing

Heeley, N. (2018) · Apollo (University of Cambridge) · doi:10.17863/cam.18622 · Cited by 1

CRE mice exhibit hyperactive and impulsive behavior affecting their learning and retention performancesPreprint

Desor, F., Hajj, A. E., Herzine, A., Djelti, F., Bombail, V., Denis, I., Oster, T., Malaplate, C., Lanhers, M., Yen, F. T., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.27.582228 · Cited by 1

The Role of Sirtuin 6 in Maintaining Vascular Integrity

Leung, S. Z. (2016) · Scholarship@Western (Western University)

Exploring Appetite and Hypothalamic Circuitry through Manipulating Gene Expression

Jois, T., & Sleeman, M. W. (2016) · Wiley eBooks · doi:10.1002/9781118839317.ch7

Central natriuretic peptide receptor (NPR)-B and peripheral lipid accumulation

Rossi, J. (2016) · Peptides · doi:10.1016/j.peptides.2016.08.003

Asleep at the Wheel: Forward Genetic ENU Mutagenesis Screen for Mouse Models of Chronic Fatigue Identifies a Mutation in Slc2a4 (GLUT4)Preprint

de Groot, M. H. M., Castorena, C. M., Kumar, V., Mohawk, J. A., Ahmed, N. I., & Takahashi, J. S. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/163378

The role of central IL-6 signalling in the development of Type 2 diabetes

Yiannakas, A. (2016) · Discovery Research Portal (University of Dundee)

Modulating Thymic Negative Selection with Bioengineered Thymus Organoids

Pradhan, I., Tajima, A., Bertera, S., Trucco, M., & Fan, Y. (2017) · CRC Press eBooks · doi:10.1201/9781315371689-4 · Cited by 1

Assessing the role of PTEN in cholinergic neurons in glucose and energy homeostasis

Rapps, J. A. (2018) · TSpace (University of Toronto)

A importância da ação do hormônio do crescimento sobre os neurônios NPY/AgPR do hipotálamo.

Couto, G. C. L. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2019.tde-17062019-165021

The role of protein tyrosine phosphatase 1b in the central regulation of energy homeostasis

Tsou, R. C. (2014) · Scholarly Commons (University of Pennsylvania)

Faculty Opinions recommendation of Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors.

Charron, F., & Yam, P. T. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737316694.793572169

Faculty Opinions recommendation of Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors.

Weiner, J. A. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737316694.793574115

Participação da via da STAT3 em neurônios POMC do hipotálamo na homeostase energética

Volpi, R. E. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2020.tde-30092022-095827

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Participação da via da PI3K em neurônios SF1 do hipotálamo na homeostase energética

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Ablation of PI3Kγ in neurons protects mice from diet-induced obesity MASLD and insulin resistance

Molinaro, A., Mazzoli, A., Gaudi, A. U., Gupta, A. C., Silva, V. R. R., Ramel, D., Laffargue, M., Ruud, J., Becattini, B., & Solinas, G. (2024) · iScience · doi:10.1016/j.isci.2024.111562

Mlc2v-Cre induces germline recombination in a sex-biased manner

Aslani, T., Abid, R., Jeyaratnam, R., Liang, W., & Kim, K.-H. (2025) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00122.2025

Knockdown of Mct1 in the arcuate nucleus increases food-anticipatory activity in mice

Martini, T., & Albrecht, U. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1642386

A Cre-mediated copy number variant compromises the reliability of a LoxP-STOP-LoxP - PLAG1 driven brain tumor model

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Transgenic dCas9-DNMT3A mouse lines enable ex vivo and in vivo methylation editing with locus-dependent transcriptional effectsPreprint

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GPR75 genetic manipulations in mice reveal central mechanism for weight loss independent of developmental effects

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Nestin-Cre Mouse Lines: A User Guide for CNS Genetics

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Pancreas-Specific Cre Driver Lines and Considerations for Their Prudent Use

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The Cre/Lox System to Assess the Development of the Mouse Brain.

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Tetracycline response element driven Cre causes ectopic recombinase activity independent of transactivator element

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