Bmf: A Proapoptotic BH3-Only Protein Regulated by Interaction with the Myosin V Actin Motor Complex, Activated by Anoikis

Serine Phosphorylation of Death Agonist BAD in Response to Survival Factor Results in Binding to 14-3-3 Not BCL-XL

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PUMA, a Novel Proapoptotic Gene, Is Induced by p53

Nakano, K., & Vousden, K. H. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00214-3 · Cited by 2,315

Noxa, a BH3-Only Member of the Bcl-2 Family and Candidate Mediator of p53-Induced Apoptosis

Oda, E., Ohki, R., Murasawa, H., Nemoto, J., Shibue, T., Yamashita, T., Tokino, T., Taniguchi, T., & Tanaka, †. N. (2000) · Science · doi:10.1126/science.288.5468.1053 · Cited by 2,112

Hidden Markov Models in Computational Biology

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Proapoptotic Bcl-2 Relative Bim Required for Certain Apoptotic Responses, Leukocyte Homeostasis, and to Preclude Autoimmunity

Bouillet, P., Metcalf, D., Huang, D. C. S., Tarlinton, D. M., Kay, T. W. H., Köntgen, F., Adams, J. M., & Strasser, A. (1999) · Science · doi:10.1126/science.286.5445.1735 · Cited by 1,504

BH1 and BH2 domains of Bcl-2 are required for inhibition of apoptosis and heterodimerization with Bax

Yin, X.-M., Oltvai, Z., & Korsmeyer, S. (1994) · Nature · doi:10.1038/369321a0 · Cited by 1,383

PUMA Induces the Rapid Apoptosis of Colorectal Cancer Cells

Yu, J., Zhang, L., Hwang, P. M., Kinzler, K. W., & Vogelstein, B. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00213-1 · Cited by 1,289

Bim: a novel member of the Bcl‐2 family that promotes apoptosis

O’Connor, L., Strasser, A., O’Reilly, L. A., Hausmann, G., Adams, J. M., Cory, S., & Huang, D. C. S. (1998) · The EMBO Journal · doi:10.1093/emboj/17.2.384 · Cited by 1,163

Integrins and anoikis

Frisch, S. M., & Ruoslahti, E. I. (1997) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(97)80124-x · Cited by 1,159

The Proapoptotic Activity of the Bcl-2 Family Member Bim Is Regulated by Interaction with the Dynein Motor Complex

Puthalakath, H., Huang, D. C. S., O'REILLY, L. A., King, S. M., & Strasser, A. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80456-6 · Cited by 1,053

Alterations in cellular metabolic pathway and epithelial cell maturation induced by MYO5B defects are partially reversible by LPAR5 activation

Momoh, M., Rathan-Kumar, S., Burman, A., Brown, M. E., Adeniran, F., Ramos, C., Goldenring, J. R., Roland, J. T., & Kaji, I. (2024) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00091.2024 · Cited by 5

The esoteric roles of Bcl-2 family proteins in glucose homeostasis and cell survival

Pfeiffer, S. L., & Prehn, J. H. M. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.320 · Cited by 5

Expression of the protein inhibitor of nitric oxide synthase in the adult rat retina before and after optic nerve lesion

Dietz, G. P. H., Schott, M., Labes, M., & Bähr, M. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.01.011 · Cited by 5

Purkinje cell loss in the cerebellum of ataxic mutant mouse, dilute-lethal: A fractionator study

Sawada, K., Sakata‐Haga, H., Jeong, Y., Azad, M. A. K., Ohkita, S., & Fukui, Y. (2004) · Congenital Anomalies · doi:10.1111/j.1741-4520.2004.00039.x · Cited by 5

Mitochondrial Outer Membrane Permeabilization

Parsons, M. J., & Green, D. R. (2009) · Wiley eBooks · doi:10.1002/9780470015902.a0021576 · Cited by 4

Does cytoskeleton ‘Akt’ in apoptosis?

Rodolfo, C., & Piacentini, M. (2002) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401039 · Cited by 5

Injectable hydrogel induces tumor cell extracellular calcification and bone regeneration to disrupt the osteolytic vicious cycle in bone metastasis

Lin, M., Deng, S., Liang, S., Jiang, Y., Chen, Q., Chen, G., Li, B., Cai, Y., Xie, X., Shuai, X., et al. (2026) · Journal of Controlled Release · doi:10.1016/j.jconrel.2026.114701 · Cited by 4

COL1A1 promotes cell proliferation, cell cycle progression, and anoikis resistance in granulosa cells of chicken pre-ovulatory follicles

Li, X., Luo, X., Zhang, X., Guo, Y., Lu, C., Cheng, M., Tang, S., & Gong, Y. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.141524 · Cited by 4

Targeting multifunctional magnetic nanowires for drug delivery in cancer cell death: an emerging paradigm

Singh, S., Rani, H., Sharma, N., Behl, T., Zahoor, I., Makeen, H. A., Albratty, M., Alhazm, H. A., & Aleya, L. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-26650-w · Cited by 4

Targeting Bcl-2 with Indole Scaffolds: Emerging Drug Design Strategies for Cancer Treatment

Zarrin, P., & Ateş‐Alagöz, Z. (2024) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/0113895575306176240925094457 · Cited by 4

Switching on and Off the Cell Death Cascade: African Swine Fever Virus Apoptosis Regulation

Hernáez, B., Escribano, J. M., & Alonso, C. (2004) · Progress in molecular and subcellular biology · doi:10.1007/978-3-540-74264-7_4 · Cited by 4

Filamin A regulates caspase-3 cleavage in platelets in a protein kinase C (PKC)-dependent manner

Silva, E. D., Devine, D. V., Jan, E., Roskelley, C. D., & Kim, H. (2022) · Biochemical Journal · doi:10.1042/bcj20220177 · Cited by 4

Cytoskeleton inhibitors combined with TRAIL induce apoptosis in HeLa carcinoma cells overexpressing antiapoptotic protein Bcl-2

Gasparian, M. E., Domnina, L. V., Ivanova, O. Y., Izyumov, D. S., Lomakin, A. J., Popova, E. N., Yagolovich, A. V., Pletjushkina, O. Y., Dolgikh, D. A., & Chernyak, B. V. (2008) · Biochemistry (Moscow) · doi:10.1134/s000629790803019x · Cited by 4

Apoptosis, senescence and cancer (cancer drug discovery and development)

Young, A. R. J. (2009) · British Journal of Cancer · doi:10.1038/sj.bjc.6604944 · Cited by 4

Construction of a prostate adenocarcinoma molecular classification: integrating spatial transcriptomics with retrospective cohort validation

Lu, B., Liu, Y., Ji, G., Yao, Y., Yang, Z., Zhu, B., Wang, L., Dong, K., Li, Y., Shi, J., et al. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06661-6 · Cited by 3

Apoptosis in platelets is independent of the actin cytoskeleton

Silva, E. D., Paul, M., & Kim, H. (2022) · PLoS ONE · doi:10.1371/journal.pone.0276584 · Cited by 3

Therapeutics targeting BCL2 family proteins

Dai, H., Meng, X. W., Ye, K., Jia, J., & Kaufmann, S. H. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-814208-0.00007-5 · Cited by 2

Microtubule Damaging Agents and Apoptosis

Carré, M., & Braguer, D. (2009) · Humana Press eBooks · doi:10.1007/978-1-59745-336-3_18 · Cited by 3

Characterization of the BH3 protein Bmf in Gallus gallus: Identification of a novel chicken-specific isoform

Gómez‐Esquer, F., Palomar, M., Rivas, I., Delcán, J., Linares, R., & Díaz‐Gil, G. (2007) · Gene · doi:10.1016/j.gene.2007.09.014 · Cited by 3

Argonaute2 is a potential target for siRNA-based cancer therapy for HT1080 human fibrosarcoma

Tagami, T., Suzuki, T., Hirose, K., Barichello, J. M., Yamazaki, N., Asai, T., Oku, N., Ishida, T., & Kiwada, H. (2011) · Drug Delivery and Translational Research · doi:10.1007/s13346-011-0025-3 · Cited by 3

Neospora caninum cytoplasmic dynein LC8 light chain 2 (NcDYNLL2) is differentially produced by pathogenically distinct isolates and regulates the host immune response

Cao, L., Fetterer, R. H., Qu, G., Zhang, X., & Tuo, W. (2018) · Parasitology · doi:10.1017/s003118201800207x · Cited by 3

Apostosis Signaling: A Means to an End

Pagliari, L. J., Pinkoski, M. J., & Green, D. R. (2003) · Elsevier eBooks · doi:10.1016/b978-012124546-7/50694-x · Cited by 3

Cell Stress-Associated Caspase Activation: Intrinsically Complex?

Creagh, E. M., & Martin, S. J. (2003) · Science Signaling · doi:10.1126/scisignal.1752003pe11 · Cited by 3

The Role of the BCL2 Family in Targeted Anticancer Response as Apoptotic Mediators

Roufayel, R., & Abdullah, S. (2025) · The Open Medicinal Chemistry Journal · doi:10.2174/0118741045413023251029095309 · Cited by 2

Dynein light chain LC8 alleviates nonalcoholic steatohepatitis by inhibiting NF‐κB signaling and reducing oxidative stress

Lee, G., Lee, H. I., Kim, N., Lee, J., Kwon, M., Kang, Y. H., Song, H. J., Yeo, C., & Jeong, W. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30811 · Cited by 2

LncRNA RP11-521C20.3 Inhibits Cigarette Smoke Extract-Induced Apoptosis in A549 Cells by Targeting BMF Signaling

Zhong, Y., Li, C., Xiang, Y., Zhou, J., & Zhang, J. (2023) · International Journal of COPD · doi:10.2147/copd.s395568 · Cited by 2

Development and validation of multi-omic prognostic signature of anoikis-related genes in liver hepatocellular carcinoma

Ding, D., Wang, D., & Qin, Y. (2023) · Medicine · doi:10.1097/md.0000000000036190 · Cited by 2

N-Acetylcysteine Alters Disease Progression and Increases Janus Kinase Mutation Frequency in a Mouse Model of Precursor B-Cell Acute Lymphoblastic Leukemia

Sams, M. P., Iansavitchous, J., Astridge, M., Rysan, H., Xu, L., de Oliveira, B. R., & DeKoter, R. P. (2024) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.123.002000 · Cited by 2

Roles of PANoptosis and related genes in acute liver failure: neoteric insight from bioinformatics analysis and animal experiment verification

Ge, T., Chen, Y., Pang, L., Shao, J., & Chen, Z. (2025) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2300678 · Cited by 2

The Intrinsic (Mitochondrial) Death Pathway and New Cancer Therapeutics: Bcl-2 Family in Focus

Shangary, S. K., Oliver, C. L., & Johnson, D. E. (2006) · Springer eBooks · doi:10.1007/0-387-23695-3_5 · Cited by 2

The Bcl-2 Family Proteins

Ding, W. J., & Yin, X. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-381-7_2 · Cited by 2

The Mitochondrial Pathway: Focus on Shape Changes

Campello, S., & Scorrano, L. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-381-7_6 · Cited by 2

Multi-probe RPA template sets to study RNA modulation and transcriptional control of BH3-only members of the Bcl-2 family

Wang, D., McDonnell, M. A., & Kelekar, A. (2005) · Cancer Detection and Prevention · doi:10.1016/j.cdp.2004.12.002 · Cited by 3

Estudo do efeito da fração BRVD obtida a partir da própolis brasileira tipificada, na proliferação de células tumorais

Costa, M. S. E. (2007) · doi:10.11606/d.5.2007.tde-20022009-134007 · Cited by 2

Bcl-2 Family Members in Hepatocellular Carcinoma (HCC) – Mechanisms and Therapeutic Potentials

Ma, S., Chen, G. Y., & Lai, P. B. S. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9597-9_9 · Cited by 2

Computational and Experimental Investigation of the Critical Behavior Observed in Cell Signaling Related to Electrically Perturbed Lipid Systems

Goswami, I. (2018) · VTechWorks (Virginia Tech) · Cited by 2

miR125-Centered ceRNETs in Breast Cancer. Clinical, Molecular and Ethical Aspects in Personalized MedicinePreprint

Piergentili, R., Gullo, G., Cucinella, G., López, A., Napoletano, G., Marinelli, E., & Zaami, S. (2023) · Preprints.org · doi:10.20944/preprints202309.1713.v1 · Cited by 1

BCL-XL dependence is a subtype agnostic actionable feature of difficult-to-treat kidney cancers

Basuroy, T., Grubb, T. M., Sadagopan, A., Qin, X., Madison, K., Hall, A., Willard, B. B., Vanharanta, S., Sarosiek, K. A., Viswanathan, S. R., et al. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-09262-3 · Cited by 1

Altered Apoptosis in AML

Mesa, R. A., & Kaufmann, S. H. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-322-6_6 · Cited by 1

Apoptosis and appearance of multinuclear C6 glioma cells after treatment by microtubule poisons

Mirčić, A., Vilimanovic, U., Brajušković, G. N., & Bumbaširević, V. (2012) · Acta veterinaria · doi:10.2298/avb1201017m · Cited by 1

Apoptosis

Wible, D. J., & Bratton, S. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65424-7 · Cited by 1

Apoptosis neuronal: la diversidad de señales y de tipos celulares

Becerra, L. V., & Pimienta, H. J. (2009) · TSpace (University of Toronto) · Cited by 1

Expression profiles of the apoptosis signaling pathway mediated by death receptor and endoplasmic reticulum in rat liver regeneration

Xing, X., Li, M. H., Zhu, X. S., & Xu, C. S. (2016) · Genetics and Molecular Research · doi:10.4238/gmr.15028288 · Cited by 1

Structural analysis of dynein intermediate and light chains

Williams, J. C., Siglin, A. E., Lightcap, C. M., & Dawn, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809470-9.00003-5 · Cited by 1

How Cancer Cells Escape Death

Werner, E. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-435-3_12 · Cited by 1

Bax, Bak and Bid: Key Mediators of Apoptosis

Dempsey, C. E., Roberts, D. L., & Dive, C. (2006) · doi:10.1002/9783527619665.ch12 · Cited by 1

Creating a protein-protein interaction network for alpha-synuclein

Könn, M. (2012) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-7491 · Cited by 1

Molecular and cellular studies of Drosophila neuroserpin Spn4A and its polymer-forming mutants

Lai, C. C.-L. (2010) · cIRcle (University of British Columbia) · doi:10.14288/1.0071181 · Cited by 1

Multiple outcomes for PI3K/Akt/mTOR targeting in non-Hodgkin lymphoma

Müller, A. (2015) · edoc Publication server (Humboldt University of Berlin) · doi:10.18452/17284 · Cited by 1

Bcl-2 Family Proteins: Master Regulators of Apoptosis

Yin, X., Ding, W., & Zhao, Y. (2003) · Humana Press eBooks · doi:10.1385/1-59259-361-5:13 · Cited by 1

BH3 ‐Only Proteins

Tuzlak, S., & Villunger, A. (2016) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0021569.pub2 · Cited by 1

Cisplatin-resistance and cell death in malignant pleural mesothelioma cells

Janson, V. (2008) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1

Allosteric SHP2 Inhibition Increases Apoptotic Dependency on BCL2 and Synergizes with Venetoclax in FLT3- and KIT- Mutant AMLPreprint

Popescu, B. O., Stahlhut, C. E., Tarver, T. C., Wishner, S., Lee, B. J., Peretz, C. A. C., Luck, C., Phojanakong, P. J., Cámara, J. A., Hongo, H., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.01.518665 · Cited by 1

Bcl-2 Family Proteins

Yin, X., Ding, W., & Zhao, Y. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-361-3_2

Expressão de um fragmento da Miosina Va inibe o crescimento de tumores de melanoma induzidos em modelo animal

Borges, A. C. (2012) · doi:10.11606/t.17.2012.tde-10022012-135441

Flexibility and specificity of the interaction of MCL-1 with BIM BH3

Fire, E. (2009) · DSpace@MIT (Massachusetts Institute of Technology)

Cloning and characterization of a dynein light chain gene from Puccinia striiformis f. sp. tritici

Liu, J., Zhang, Q., Chang, Q., Wang, Q., Han, L., Liu, J., Li, M., Zhuang, H., & Kang, Z. (2014) · Journal of Basic Microbiology · doi:10.1002/jobm.201300645

Regulation of mast cell survival and apoptosis

Karlberg, M. (2008) · Figshare

Programmed Cell Death

Vaux, D. L., & Strasser, A. (2006) · Wiley-VCH eBooks · doi:10.1002/3527600906.mcb.200400090

Role of Focal Adhesion Protein Migfilin in the Regulation of Cell Survival and Cell Cycle

Zhao, J. (2009) · D-Scholarship@Pitt (University of Pittsburgh)

MicroRNAs Regulated Brain Tumor Cell Phenotype and Their Therapeutic Potential

Zhang, C., Chen, B., Xu, X., Han, B., Wang, G., & Wang, J. (2013) · InTech eBooks · doi:10.5772/52362

BH3-Only Proteins in Cancer and Apoptosis

Ghiotto, F., Tenca, C., Fais, F., & Bruno, S. (2013) · Springer eBooks · doi:10.1007/978-94-007-6211-4_9

Manipulation of cell death pathways in cancer

Bray, K. (2011) · doi:10.7282/t3bp01xm

Study of the regulation and signalling of cdk2-Cyclin o complexes during apoptosis

Roset, R. (2008) · TDX (Tesis Doctorals en Xarxa)

ESTUDO DA IMUNOLOCALIZAÇÃO DE MIOSINA V EM TUMORES DE GLÂNGULAS SALIVARES E EPIDERMÓIDES BUCAIS

Santos, A. F. A., Mda Dias Alves Lorenna Marques, L., & Espíndola, F. S. (2009) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Factores pronósticos biológicos y clínicos en el linfoma de células del manto

Ferrer, A. (2008) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Les protéines de la famille Bcl-2 à BH3 seulement

Priault, M., & Manon, S. (2002) · médecine/sciences · doi:10.1051/medsci/2002182145

Correction: Human Embryonic Stem Cells Express Elevated Levels of Multiple Pro-Apoptotic BCL-2 Family Members

Madden, D. T., Davila-Kruger, D., Melov, S., & Bredesen, D. E. (2012) · PLoS ONE · doi:10.1371/annotation/38d5bc7f-42f2-4d1e-b293-1a003bb57812

Hold on for dear life

Leslie, M. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.1732fta3

N-Bak : a Neuron-Specific Splice Variant of Bak with anti-Apoptotic Properties

Sun, Y. (2003) · Työväentutkimus Vuosikirja

Regulation of UV induced apoptosis in human melanocytes

Bivik, C. A. (2007) · DiVA (Linkoping University)

The Bax -/- Bak -/- Mouse: a Model for Apoptosis

Zong, W., Rathmell, J. C., Golden, J. A., & Lindsten, T. (2003) · Springer eBooks · doi:10.1007/978-1-4757-5890-0_9

Stimulation der erythrozytären Exposition von Phosphatidylserin durch Quecksilberionen

Lang, F. J. W. (2006)

EPIGENETIC SILENCING OF THE PROAPOPTOTIC GENE BIM IN ANAPLASTIC

Mogavero, A. (2010)

Characterization of Myosin protein(s) of Leishmania donovani

SanthaRam, K. S. (2009) · INFLIBNET

Chapter 9 The Bax-1-Bak-l - Mouse: a Model for Apoptosis

Zong, W., Rathmell, J. C., & Golden, J. A. (2003)

Construction of cDNA library of Andrias davidianus skin tissue and molecular cloning and expression analysis of Dynll 2 gene

Wang, L., Zheng, Y., Li, F., Li, W., & Liu, X. (2012) · JOURNAL OF FISHERIES OF CHINA · doi:10.3724/sp.j.1231.2011.17333

Insights into p53-Dependent Apoptotic Signaling and Cell Fate vis-a-vis Functional Cooperation among BCL-xL, Cytoplasmic p53, and PUMA

Fisher, J. (2011) · doi:10.21007/etd.cghs.2011.0094

Tipping the Balance between Chemosensitivity and Chemoresistance

Zutter, M. M. (2007)

Apoptosis in Critical Conditions

Golubev, A. M., Severin, E. S., Vesnyanko, T. P., Alkadarsky, A. S., & Poroshenko, G. G. (2006)

Expression des protein inhibitor of nitric oxide synthase in der Retina adulter Ratten

Neurologie, A. A., & DICHGANS, J. (2003)

Sistemas líquido cristalinos de geleificação in situ de administração intratumoral para liberação localizada de siRNA na terapia do câncer de pele

Cardoso, L. N. B. (2016) · doi:10.11606/t.60.2016.tde-05102016-093552

Avaliação dos efeitos antitumorais da metaloproteinase ofídica jararagina no adenocarcinoma de mama.

Palomino, M. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.87.2012.tde-17122014-110755

Apoptosis and Apoptotic Factors (BCL2 and Bax Protein) in Recurrent Benign Nasal Polyp

Ali, M. H., & Hameed, H. M. (2009) · Medical Journal of Babylon

Regulation of anoikis by ankyrin complexes

Kumar, S. (2010) · doi:10.33915/etd.4620

Efecto de la administración de PPI-2458 sobre los procesos de proliferación celular y apoptosis en un modelo in vitro de hepatocarcinoma = Effect of treatment with PPI-2458 on cell proliferation and apoptosis processes in an in vitro model of Hepatocarcinoma

Martín‐Renedo, J. (2011) · Buleria (Universidad de León) · doi:10.18002/10612/1751

The Role of the Bcl‐2 Protein Family in Tumorigenesis and Cancer Therapy

Naik, E., & Strasser, A. (2006) · Wiley eBooks · doi:10.1002/9783527619665.ch11

MYB IS Required for B-Selection During Thymopoises

Duley, A. K. (2009) · doi:10.18130/v3x28d

Efeito do lincRNA PVT1 associado ao potenciador de zeste homólogo 2 (EZH2) e ao receptor de andrógeno (AR) sobre a expressão gênica em larga escala em células LNCaP de câncer de próstata

Videira, A. (2019) · doi:10.11606/t.46.2019.tde-24102019-104009

Bmf Facilitates Protein Degradation and Reduces Beclin1 Ubiquitination to Inhibit Autophagy Independent of mTORPreprint

Delgado-Vergas, M., Fort, S., Tassew, D., & Tesfaigzi, Y. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.02.892828

Apoptosis

Malladi, S., Challa-Malladi, M., & Bratton, S. B. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-046884-6.00231-1 · Cited by 1

Characterizing the Mechanism of Cul7-mediated Inhibition of Cell Death

Oliveri, S. (2011) · TSpace (University of Toronto)

BAD Phosphorylation: A Novel Link between Apoptosis and Cancer

Polzien, L. (2011)

Caracterização funcional e da dinâmica espacial da miosina-Va no processo de fissão mitocondrial

Araujo, J. S. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2021.tde-11062021-090108

Bcl-2 Family Evolutionary Conservation

Kvansakul, M., Suraweera, C. D., Banjara, S., & Hinds, M. G. (2021)

Dynein Light Chain LC8 Alleviates Nonalcoholic Steatohepatitis By Regulating Nuclear Factor κB Through Interference With IκBα PhosphorylationPreprint

Lee, G., Lee, H. I., Kim, N., Lee, J., Kwon, M., Kang, Y. H., Song, H. J., Yeo, C., & Jeong, W. (2021) · Research Square · doi:10.21203/rs.3.rs-906706/v1

Faculty Opinions recommendation of Loss of the BH3-only protein Bmf impairs B cell homeostasis and accelerates gamma irradiation-induced thymic lymphoma development.

Hayakawa, K. (2008) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1104067.560044

Participação da cadeia leve de dineína 2, DYNLL2, na dinâmica de montagem e desmontagem do cílio primário

Iturralde, S. A. G. (2021) · doi:10.11606/d.17.2021.tde-28012022-115436

The role of histone 2B monoubiquitination (H2Bub1) in HER2-driven mammary carcinoma

Prokakis, E. (2021) · doi:10.53846/goediss-8486

The Role of the Tumor Suppressor, p190RhoGAP, in Apoptosis and Cytokinesis

Ludwig, K. (2011) · doi:10.18130/v3k857

R EPORTS Bmf: A Proapoptotic BH3-Only Protein Regulated by Interaction with the Myosin V Actin Motor Complex, Activated by Anoikis

Puthalakath, H., Villunger, A., O’reilly, L. A., Beaumont, J. G., Coultas, L., Cheney, R. E., Huang, D. C. S., & Strasser, A. (2013)

Cells Hang on for Dear Life

(2001) · Science Signaling · doi:10.1126/scisignal.992001tw327

The Proapoptotic Activity of the Bcl-2 Family Member Bim Is Regulated by Interaction with the Dynein Motor Complex

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