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Nongenomic Testosterone Calcium Signaling

https://doi.org/10.1074/jbc.m202997200
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Progesterone triggers rapid transmembrane calcium influx and/or calcium mobilization from endoplasmic reticulum, via a pertussis-insensitive G-protein in granulosa cells in relation to luteinization process
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Differential activation of c‐fos promoter elements by serum, lysophosphatidic acid, G proteins and polypeptide growth factors.
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Tyrosine kinase/p21ras/MAP‐kinase pathway activation by estradiol‐receptor complex in MCF‐7 cells.
inferredcites →https://doi.org/10.1002/jbmr.5650081111openalex-snapshot
Cell signaling and estrogens in female rat osteoblasts: A possible involvement of unconventional nonnuclear receptors
inferredcites →https://doi.org/10.1002/jlb.60.1.8openalex-snapshot
Endotoxin signal transduction in macrophages
inferredcites →https://doi.org/10.1006/bbrc.1998.8492openalex-snapshot
Membrane Receptors for Steroid Hormones: A Case for Specific Cell Surface Binding Sites for Vitamin D Metabolites and Estrogens
inferredcites →https://doi.org/10.1006/bbrc.2001.4341openalex-snapshot
17β-Estradiol Increases Ca2+ Influx and Down Regulates Interleukin-2 Receptor in Mouse Thymocytes
inferredcites →https://doi.org/10.1007/s001090050242openalex-snapshot
Transcriptional cross-talk, the second mode of steroid hormone receptor action
inferredcites →https://doi.org/10.1016/0092-8674(89)90237-7openalex-snapshot
Gene regulation by steroid hormones
inferredcites →https://doi.org/10.1016/0143-4160(94)90097-3openalex-snapshot
Calcium regulation of immediate-early response genes
inferredcites →https://doi.org/10.1016/0264-410x(93)90068-9openalex-snapshot
Testosterone impairs efficacy of protective vaccination against P. chabaudi malaria
inferredcites →https://doi.org/10.1016/b978-0-12-571149-4.50017-9openalex-snapshot
The Androgen Receptor: An Overview
inferredcites →https://doi.org/10.1016/s0014-5793(97)00346-3openalex-snapshot
Testosterone induces Ca2+ influx via non‐genomic surface receptors in activated T cells
inferredcites →https://doi.org/10.1016/s0014-5793(98)00039-8openalex-snapshot
Estradiol binding to cell surface raises cytosolic free calcium in T cells
inferredcites →https://doi.org/10.1016/s0021-9258(17)37270-8openalex-snapshot
Androgens increase intracellular calcium concentration and inositol 1,4,5-trisphosphate and diacylglycerol formation via a pertussis toxin-sensitive G-protein.
inferredcites →https://doi.org/10.1016/s0024-3205(00)00953-xopenalex-snapshot
Testosterone inhibits expression of inducible nitric oxide synthase in murine macrophages
inferredcites →https://doi.org/10.1016/s0026-895x(24)12026-3openalex-snapshot
Inhibition of Cardiac L-Type Calcium Channels by Epoxyeicosatrienoic Acids
inferredcites →https://doi.org/10.1016/s0026-895x(24)12172-4openalex-snapshot
p38 but Not p44/42 Mitogen-Activated Protein Kinase Is Required for Nitric Oxide Synthase Induction Mediated by Lipopolysaccharide in RAW 264.7 Macrophages
inferredcites →https://doi.org/10.1016/s0031-6997(24)01468-6openalex-snapshot
Multiple Actions of Steroid Hormones—A Focus on Rapid, Nongenomic Effects
inferredcites →https://doi.org/10.1016/s0039-128x(01)00175-1openalex-snapshot
Testosterone signaling in T cells and macrophages
inferredcites →https://doi.org/10.1016/s0092-8674(00)80357-8openalex-snapshot
A Putative Leucine-Rich Repeat Receptor Kinase Involved in Brassinosteroid Signal Transduction
inferredcites →https://doi.org/10.1016/s0092-8674(01)00268-9openalex-snapshot
Nongenotropic, Sex-Nonspecific Signaling through the Estrogen or Androgen Receptors
inferredcites →https://doi.org/10.1016/s0952-7915(99)00046-1openalex-snapshot
Tlr4: central component of the sole mammalian LPS sensor
inferredcites →https://doi.org/10.1016/s1043-2760(98)00039-3openalex-snapshot
The Androgen Receptor as Mediator of Gene Expression and Signal Transduction Pathways
inferredcites →https://doi.org/10.1038/33014openalex-snapshot
Steroids tickle cells inside and out
inferredcites →https://doi.org/10.1038/35066597openalex-snapshot
BRI1 is a critical component of a plasma-membrane receptor for plant steroids
inferredcites →https://doi.org/10.1038/369156a0openalex-snapshot
The stress-activated protein kinase subfamily of c-Jun kinases
inferredcites →https://doi.org/10.1038/sj.onc.1203032openalex-snapshot
Rapid signalling by androgen receptor in prostate cancer cells
inferredcites →https://doi.org/10.1046/j.1365-2567.1999.00747.xopenalex-snapshot
Involvement of p38 mitogen‐activated protein kinase in lipopolysaccharide‐induced iNOS and COX‐2 expression in J774 macrophages
inferredcites →https://doi.org/10.1073/pnas.93.7.2774openalex-snapshot
Activation of c-Jun N-terminal kinase in bacterial lipopolysaccharide-stimulated macrophages.
inferredcites →https://doi.org/10.1073/pnas.96.8.4686openalex-snapshot
Estrogen-induced activation of mitogen-activated protein kinase requires mobilization of intracellular calcium
inferredcites →https://doi.org/10.1074/jbc.270.28.16483openalex-snapshot
The Regulation of AP-1 Activity by Mitogen-activated Protein Kinases
inferredcites →https://doi.org/10.1074/jbc.274.34.24383openalex-snapshot
Spleen-specific Expression of the Malaria-inducible Intronless Mouse Gene imap38
inferredcites →https://doi.org/10.1074/jbc.m005492200openalex-snapshot
Estrogen Receptor-mediated Activation of the Serum Response Element in MCF-7 Cells through MAPK-dependent Phosphorylation of Elk-1
inferredcites →https://doi.org/10.1074/jbc.m009147200openalex-snapshot
Tumor Necrosis Factor-α Induction of Endothelial Ephrin A1 Expression Is Mediated by a p38 MAPK- and SAPK/JNK-dependent but Nuclear Factor-κB-independent Mechanism
inferredcites →https://doi.org/10.1074/jbc.m010311200openalex-snapshot
Androgen Receptor Specifically Interacts with a Novel p21-activated Kinase, PAK6
inferredcites →https://doi.org/10.1074/jbc.m010984200openalex-snapshot
Mechanisms of Estrogen Receptor Action in the Myocardium
inferredcites →https://doi.org/10.1074/jbc.m109808200openalex-snapshot
Estradiol-induced Nongenomic Calcium Signaling Regulates Genotropic Signaling in Macrophages
inferredcites →https://doi.org/10.1091/mbc.10.10.3113openalex-snapshot
Testosterone Signaling through Internalizable Surface Receptors in Androgen Receptor-free Macrophages
inferredcites →https://doi.org/10.1093/emboj/18.9.2500openalex-snapshot
Non‐transcriptional action of oestradiol and progestin triggers DNA synthesis
inferredcites →https://doi.org/10.1093/humupd/6.3.225openalex-snapshot
Steroid hormone receptors: an update
inferredcites →https://doi.org/10.1095/biolreprod63.3.736openalex-snapshot
Rapid Androgen Actions on Calcium Signaling in Rat Sertoli Cells and Two Human Prostatic Cell Lines: Similar Biphasic Responses Between 1 Picomolar and 100 Nanomolar Concentrations1
inferredcites →https://doi.org/10.1096/fasebj.13.1.123openalex-snapshot
Functional testosterone receptors in plasma membranes of T cells
inferredcites →https://doi.org/10.1111/j.1365-3024.1991.tb00289.xopenalex-snapshot
Testosterone and other gonadal factor(s) restrict the efficacy of genes controlling resistance to Plasmodium chabaudi malaria
inferredcites →https://doi.org/10.1126/science.288.5475.2360openalex-snapshot
Perception of Brassinosteroids by the Extracellular Domain of the Receptor Kinase BRI1
inferredcites →https://doi.org/10.1126/science.3283939openalex-snapshot
The Steroid and Thyroid Hormone Receptor Superfamily
inferredcites →https://doi.org/10.1128/iai.56.9.2400-2406.1988openalex-snapshot
Resistance to Plasmodium chabaudi in B10 mice: influence of the H-2 complex and testosterone
inferredcites →https://doi.org/10.1128/mcb.18.4.1844openalex-snapshot
Anisomycin Selectively Desensitizes Signalling Components Involved in Stress Kinase Activation and fos and jun Induction
inferredcites →https://doi.org/10.1146/annurev.biochem.67.1.753openalex-snapshot
TGF-β SIGNAL TRANSDUCTION
inferredcites →https://doi.org/10.1172/jci5347openalex-snapshot
Estrogen receptor α mediates the nongenomic activation of endothelial nitric oxide synthase by estrogen
inferredcites →https://doi.org/10.1210/edrv-16-3-271openalex-snapshot
Androgen Receptor Defects: Historical, Clinical, and Molecular Perspectives*
inferredcites →https://doi.org/10.1210/en.142.4.1669openalex-snapshot
Estradiol Signaling via Sequestrable Surface Receptors
inferredcites →https://doi.org/10.1210/endo.142.4.8094openalex-snapshot
Estradiol Signaling via Sequestrable Surface Receptors
inferredcites →https://doi.org/10.1210/me.14.10.1649openalex-snapshot
Estrogen-Induced Activation of Erk-1 and Erk-2 Requires the G Protein-Coupled Receptor Homolog, GPR30, and Occurs via Trans-Activation of the Epidermal Growth Factor Receptor through Release of HB-EGF
inferredcites →https://doi.org/10.1210/mend.16.1.0758openalex-snapshot
Estrogen Action Via the G Protein-Coupled Receptor, GPR30: Stimulation of Adenylyl Cyclase and cAMP-Mediated Attenuation of the Epidermal Growth Factor Receptor-to-MAPK Signaling Axis
inferredcites →https://doi.org/10.1530/eje.0.1350367openalex-snapshot
17β-Estradiolid Ca influx rapid Ca2+ prostate cancer cells
inferredcites →https://doi.org/10.1677/joe.0.1350407openalex-snapshot
Testosterone-induced suppression of self-healing Plasmodium chabaudi malaria: an effect not mediated by androgen receptors?
inferredcites →https://doi.org/10.1677/joe.0.1390487openalex-snapshot
Testrosterone-induced compared with oestradiol-induced immunosuppression against Plasmodium chabaudi malaria
inferredcites →https://doi.org/10.3109/10799899909036666openalex-snapshot
Calcium Signalling and Gene Expression
inferredcites →https://doi.org/10.4049/jimmunol.139.3.949openalex-snapshot
Modulations of functional activity in differentiated macrophages are accompanied by early and transient increase or decrease in c-fos gene transcription.
inferredcites →https://doi.org/10.4049/jimmunol.163.12.6403openalex-snapshot
Extracellular Signal-Related Kinase (ERK) and p38 Mitogen-Activated Protein (MAP) Kinases Differentially Regulate the Lipopolysaccharide-Mediated Induction of Inducible Nitric Oxide Synthase and IL-12 in Macrophages: Leishmania Phosphoglycans Subvert Macrophage IL-12 Production by Targeting ERK…

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Identification, Structural Characterization and Rational Agonist Design of a Gs-Coupled Androgen Membrane Receptor
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Cellular mechanism of estrogen‐induced thymic involution in wall lizard: caspase‐dependent action
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Searching For SARA
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Androgen Excess in Women and the Respiratory System
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Sex Steroid Receptors in Immune Cells
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The actions and side effects of Anabolic Steroids in sport and social abuse
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Actions et effets secondaires de l’abus de Stéroïdes Anabolisants dans le sport et la vie sociale
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Effect of Androgens and Glucocorticoids on Microbial Growth and Antimicrobial Susceptibility
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Androgens and Cardiovascular Diseases in Women
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Role of putative membrane receptors in the effects of estradiol on human vascular cell growth
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Identification, structure, and agonist design of an androgen membrane receptor
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Characterization of the pattern of the nongenomic signaling pathway through which TCDD-induces early inflammatory responses in U937 human macrophages
inferred← citeshttps://doi.org/10.1016/j.etp.2004.07.002openalex-snapshot
Testosterone influenced the expression of Notch1, Notch2 and Jagged1 induced by lipopolysaccharide in macrophages
inferred← citeshttps://doi.org/10.1016/j.eururo.2004.04.012openalex-snapshot
Prevention of Prostate Cancer by Androgens: Experimental Paradox or Clinical Reality
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Estradiol pretreatment attenuated nicotine-induced endothelial cell apoptosis via estradiol functional membrane receptor
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Rapid membrane responses to dihydrotestosterone are sex dependent in growth plate chondrocytes
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Genomic and non-genomic actions of progestogens in the breast
inferred← citeshttps://doi.org/10.1016/j.mce.2008.12.020openalex-snapshot
Dihydrotestosterone stimulates aldosterone secretion by H295R human adrenocortical cells
inferred← citeshttps://doi.org/10.1016/j.mce.2015.07.005openalex-snapshot
Detecting the presence of hippocampus membrane androgen receptors in male SAMP8 mice and their induced synaptic plasticity
inferred← citeshttps://doi.org/10.1016/j.mce.2021.111487openalex-snapshot
OXER1 mediates testosterone-induced calcium responses in prostate cancer cells
inferred← citeshttps://doi.org/10.1016/j.mednuc.2007.11.002openalex-snapshot
Évolution de la cellule normale à la cellule cancéreuse prostatique hormonodépendante–hormono-indépendante
inferred← citeshttps://doi.org/10.1016/j.micinf.2004.11.016openalex-snapshot
Testosterone responsiveness of spleen and liver in female lymphotoxin β receptor-deficient mice resistant to blood-stage malaria
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2005.10.016openalex-snapshot
Sex dimorphism in cardiac pathophysiology: Experimental findings, hormonal mechanisms, and molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2010.01.007openalex-snapshot
Membrane androgen receptors may mediate androgen reinforcement
inferred← citeshttps://doi.org/10.1016/j.steroids.2004.05.007openalex-snapshot
Rapid effects of androgens in macrophages
inferred← citeshttps://doi.org/10.1016/j.steroids.2008.11.017openalex-snapshot
Molecular mechanisms of testosterone action in spermatogenesis☆
inferred← citeshttps://doi.org/10.1016/j.steroids.2010.06.010openalex-snapshot
Testosterone-induced upregulation of miRNAs in the female mouse liver
inferred← citeshttps://doi.org/10.1016/j.steroids.2011.02.016openalex-snapshot
Understanding extranuclear (nongenomic) androgen signaling: What a frog oocyte can tell us about human biology
inferred← citeshttps://doi.org/10.1016/j.steroids.2011.08.001openalex-snapshot
Role of 17β-estradiol and testosterone in apoptosis
inferred← citeshttps://doi.org/10.1016/j.steroids.2011.10.014openalex-snapshot
Non-classic androgen actions in Sertoli cell membrane in whole seminiferous tubules: Effects of nandrolone decanoate and catechin
inferred← citeshttps://doi.org/10.1016/j.surg.2005.03.020openalex-snapshot
The influence of gender on human innate immunity
inferred← citeshttps://doi.org/10.1016/j.tem.2005.06.002openalex-snapshot
Membrane rafts as potential sites of nongenomic hormonal signaling in prostate cancer
inferred← citeshttps://doi.org/10.1016/j.tem.2007.09.004openalex-snapshot
Non-classical actions of testosterone: an update
inferred← citeshttps://doi.org/10.1016/j.yexcr.2006.04.023openalex-snapshot
Neuronal differentiation of PC12 cells abolishes the expression of membrane androgen receptors
inferred← citeshttps://doi.org/10.1016/j.yfrne.2007.08.004openalex-snapshot
Rapid actions of androgens
inferred← citeshttps://doi.org/10.1016/j.yfrne.2007.10.005openalex-snapshot
Non-genomic actions of androgens
inferred← citeshttps://doi.org/10.1016/j.yfrne.2016.02.003openalex-snapshot
Gonadal hormone modulation of intracellular calcium as a mechanism of neuroprotection
inferred← citeshttps://doi.org/10.1017/cbo9781139003353.003openalex-snapshot
Testosterone: biosynthesis, transport, metabolism and (non-genomic) actions
inferred← citeshttps://doi.org/10.1038/sj.bjp.0705141openalex-snapshot
The vasodilatory action of testosterone: a potassium‐channel opening or a calcium antagonistic action?
inferred← citeshttps://doi.org/10.1055/s-2007-973427openalex-snapshot
Receptor Mechanisms Mediating Non-Genomic Actions of Sex Steroids
inferred← citeshttps://doi.org/10.1083/jcb.200409011openalex-snapshot
Nontranscriptional modulation of intracellular Ca2+ signaling by ligand stimulated thyroid hormone receptor
inferred← citeshttps://doi.org/10.1093/toxsci/kfg150openalex-snapshot
Antiandrogenic Effects of Bisphenol A and Nonylphenol on the Function of Androgen Receptor
inferred← citeshttps://doi.org/10.1096/fj.03-0328comopenalex-snapshot
Membrane glucocorticoid receptors (mGCR) are expressed in normal human peripheral blood mononuclear cells and up‐regulated after in vitro stimulation and in patients with rheumatoid arthritis
inferred← citeshttps://doi.org/10.1096/fj.202002526rropenalex-snapshot
Management of cardiometabolic complications in polycystic ovary syndrome: Unmet needs
inferred← citeshttps://doi.org/10.1097/mbc.0b013e328337b475openalex-snapshot
Mitogen-activated protein kinases pathway is involved in physiological testosterone-induced tissue factor pathway inhibitor expression in endothelial cells
inferred← citeshttps://doi.org/10.1111/aji.12363openalex-snapshot
Influence of Testosterone on Inflammatory Response in Testicular Cells and Expression of Transcription Factor Foxp3 in T Cells
inferred← citeshttps://doi.org/10.1111/cns.12757openalex-snapshot
Androgen alleviates neurotoxicity of β‐amyloid peptide (Aβ) by promoting microglial clearance of Aβ and inhibiting microglial inflammatory response to Aβ
inferred← citeshttps://doi.org/10.1111/j.1365-2265.2011.03969.xopenalex-snapshot
Dyslipidaemia is associated with testosterone, oestradiol and androgen receptor CAG repeat polymorphism in men with type 2 diabetes
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2005.03318.xopenalex-snapshot
Androgens activate mitogen‐activated protein kinase signaling: Role in neuroprotection
inferred← citeshttps://doi.org/10.1128/iai.73.1.436-443.2005openalex-snapshot
Testosterone Suppresses Protective Responses of the Liver to Blood-Stage Malaria
inferred← citeshttps://doi.org/10.1134/s0006297913120043openalex-snapshot
Effect of sex hormones on levels of mRNAs coding for proteins involved in lipid metabolism in macrophages
inferred← citeshttps://doi.org/10.1152/ajpendo.00035.2003openalex-snapshot
Sex-specific p38 MAP kinase activation following trauma-hemorrhage: involvement of testosterone and estradiol
inferred← citeshttps://doi.org/10.1161/circulationaha.107.708768openalex-snapshot
Physiological Testosterone Replacement Therapy Attenuates Fatty Streak Formation and Improves High-Density Lipoprotein Cholesterol in the Tfm Mouse
inferred← citeshttps://doi.org/10.1177/153537020322801106openalex-snapshot
Proteins of Multiple Classes May Participate in Nongenomic Steroid Actions
inferred← citeshttps://doi.org/10.1186/1476-511x-11-168openalex-snapshot
Dihydrotestosterone regulating apolipoprotein M expression mediates via protein kinase C in HepG2 cells
inferred← citeshttps://doi.org/10.1210/en.2005-1139openalex-snapshot
Testosterone Induces an Intracellular Calcium Increase by a Nongenomic Mechanism in Cultured Rat Cardiac Myocytes
inferred← citeshttps://doi.org/10.1210/en.2005-1243openalex-snapshot
Selective Inhibition of L-Type Ca2+ Channels in A7r5 Cells by Physiological Levels of Testosterone
inferred← citeshttps://doi.org/10.1210/en.2006-1200openalex-snapshot
Androgen-Mediated Immune Function Is Altered by the Apolipoprotein E Gene
inferred← citeshttps://doi.org/10.1210/en.2006-1465openalex-snapshot
Testosterone Activates Mitogen-Activated Protein Kinase via Src Kinase and the Epidermal Growth Factor Receptor in Sertoli Cells
inferred← citeshttps://doi.org/10.1210/en.2014-1198openalex-snapshot
Identification and Characterization of Membrane Androgen Receptors in the ZIP9 Zinc Transporter Subfamily: I. Discovery in Female Atlantic Croaker and Evidence ZIP9 Mediates Testosterone-Induced Apoptosis of Ovarian Follicle Cells
inferred← citeshttps://doi.org/10.1210/en.2014-1201openalex-snapshot
Identification and Characterization of Membrane Androgen Receptors in the ZIP9 Zinc Transporter Subfamily: II. Role of Human ZIP9 in Testosterone-Induced Prostate and Breast Cancer Cell Apoptosis
inferred← citeshttps://doi.org/10.1210/en.2018-00987openalex-snapshot
Membrane Androgen Receptors Unrelated to Nuclear Steroid Receptors
inferred← citeshttps://doi.org/10.1210/en.2019-00367openalex-snapshot
Dihydrotestosterone increases cytotoxic activity of macrophages on prostate cancer cells via TRAIL
inferred← citeshttps://doi.org/10.1210/er.2003-0005openalex-snapshot
Androgens and Cardiovascular Disease
inferred← citeshttps://doi.org/10.1210/me.2009-0472openalex-snapshot
Androgens Induce Nongenomic Stimulation of Colonic Contractile Activity through Induction of Calcium Sensitization and Phosphorylation of LC20 and CPI-17
inferred← citeshttps://doi.org/10.1242/dev.204390openalex-snapshot
Testosterone acts through the membrane protein GPRC6A to cause cardiac edema in zebrafish embryos
inferred← citeshttps://doi.org/10.1517/14712598.7.7.1093openalex-snapshot
Testosterone treatment to mimic hormone physiology in androgen replacement therapy
inferred← citeshttps://doi.org/10.1517/14728222.2013.806491openalex-snapshot
Targeting membrane androgen receptors in tumors
inferred← citeshttps://doi.org/10.1530/eje.0.1480281openalex-snapshot
Non-genomic actions of sex steroid hormones
inferred← citeshttps://doi.org/10.1677/jme-10-0026openalex-snapshot
Testosterone-induced permanent changes of hepatic gene expression in female mice sustained during Plasmodium chabaudi malaria infection
inferred← citeshttps://doi.org/10.2174/156802611796117667openalex-snapshot
A Single Pill to Treat Postmenopausal Hypertension? Not Yet
inferred← citeshttps://doi.org/10.3109/15622970309167905openalex-snapshot
Testosterone Deficiency and Mood in Aging Men: Pathogenic and Therapeutic Interactions
inferred← citeshttps://doi.org/10.3892/ijmm.2017.3149openalex-snapshot
Effects of testosterone and 17β-estradiol on angiotensin-induced changes in tyrosine kinase activity in the androgen-independent human prostate cancer cell line, DU145
inferred← citeshttps://doi.org/10.3978/j.issn.2223-4683.2013.09.07openalex-snapshot
Androgen receptor-mediated non-genomic regulation of prostate cancer cell proliferation.
inferred← citeshttps://doi.org/10.4049/jimmunol.177.1.621openalex-snapshot
Gender Differences in Murine Airway Responsiveness and Lipopolysaccharide-Induced Inflammation
inferred← citeshttps://doi.org/10.4172/2157-7536.s2-005openalex-snapshot
Androgens Rapidly Activate Nuclear Factor-Kappa B via Intracellular Ca2+ Signalling in Human Vascular Endothelial Cells
inferred← citeshttps://doi.org/10.5772/28243openalex-snapshot
Androgen Deprivation Therapy for Prostate Cancer
inferred← citeshttps://doi.org/10.5772/53648openalex-snapshot
Female Salivary Testosterone: Measurement, Challenges and Applications
inferred← citeshttps://doi.org/10.5958/j.2277-3371.4.1.004openalex-snapshot
New Emerging Androgenic Actions in the Regulation of Sperm Production and Function
inferred← citeshttps://doi.org/10.70675/cee355aez4f3cz472bz8dd9z2880a141df1copenalex-snapshot
Dérégulation de la signalisation non génomique du récepteur aux androgènes dans un modèle SBMA in vitro
inferred← citeshttps://doi.org/10.7705/biomedica.v29i4.140openalex-snapshot
Actividad inducida por androsterona y hemisuccinato de androsterona sobre la presión de perfusión y la resistencia vascular
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