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WKP|Q42886767
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(OCoLC)Q42886767
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Paul Foster
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Paul Foster
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670
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Author's 17beta-hydroxysteroid dehydrogenase Type 1, and not Type 12, is a target for endocrine therapy of hormone-dependent breast cancer.
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670
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Author's 1H NMR-MS-based heterocovariance as a drug discovery tool for fishing bioactive compounds out of a complex mixture of structural analogues
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670
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Author's A comparative study of the ability of calcitonin gene-related peptide and adrenomedullin(13 - 52) to modulate microvascular but not thermal hyperalgesia responses
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670
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Author's A new micronized formulation of 2-methoxyestradiol-bis-sulfamate
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670
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Author's A new micronized formulation of 2-methoxyestradiol-bis-sulfamate (STX140) is therapeutically potent against breast cancer.
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670
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‡a
Author's A new therapeutic strategy against hormone-dependent breast cancer: the preclinical development of a dual aromatase and sulfatase inhibitor
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670
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Author's Anticancer steroid sulfatase inhibitors: synthesis of a potent fluorinated second-generation agent, in vitro and in vivo activities, molecular modeling, and protein crystallography
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670
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‡a
Author's Antiinflammatory activity of soluble guanylate cyclase: cGMP-dependent down-regulation of P-selectin expression and leukocyte recruitment.
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670
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Author's BCRP expression does not result in resistance to STX140 in vivo, despite the increased expression of BCRP in A2780 cells in vitro after long-term STX140 exposure.
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670
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‡a
Author's C-type natriuretic peptide inhibits leukocyte recruitment and platelet-leukocyte interactions via suppression of P-selectin expression
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670
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Author's Chimeric microtubule disruptors
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670
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‡a
Author's Design, synthesis, and biological evaluation of new arylamide derivatives possessing sulfonate or sulfamate moieties as steroid sulfatase enzyme inhibitors
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670
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‡a
Author's Development of hormone-dependent prostate cancer models for the evaluation of inhibitors of 17beta-hydroxysteroid dehydrogenase type 3.
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670
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Author's Efficacy of three potent steroid sulfatase inhibitors: pre-clinical investigations for their use in the treatment of hormone-dependent breast cancer.
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670
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Author's Endothelial cells play an essential role in the thermal hyperalgesia induced by nerve growth factor.
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670
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‡a
Author's Estrogen Activation by Steroid Sulfatase Increases Colorectal Cancer Proliferation via GPER.
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670
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Author's Estrone Sulfate Transport and Steroid Sulfatase Activity in Colorectal Cancer: Implications for Hormone Replacement Therapy
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670
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Author's In touch with your feminine side: how oestrogen metabolism impacts prostate cancer
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670
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Author's In vivo and in vitro properties of STX2484: a novel non-steroidal anti-cancer compound active in taxane-resistant breast cancer
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670
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Author's In vivo efficacy of STX213, a second-generation steroid sulfatase inhibitor, for hormone-dependent breast cancer therapy.
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670
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Author's In vivo inhibition of angiogenesis by sulphamoylated derivatives of 2-methoxyoestradiol
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670
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Author's NNT is a key regulator of adrenal redox homeostasis and steroidogenesis in male mice.
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670
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Author's Oestrogen and colorectal cancer: mechanisms and controversies
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670
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Author's Recent developments of steroid sulfatase inhibitors as anti-cancer agents.
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670
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Author's Steroid sulfatase inhibitors for estrogen- and androgen-dependent cancers
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670
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Author's Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents
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670
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Author's STX140, but not paclitaxel, inhibits mammary tumour initiation and progression in C3(1)/SV40 T/t-antigen transgenic mice
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670
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Author's STX140 is efficacious in vitro and in vivo in taxane-resistant breast carcinoma cells.
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670
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Author's STX2171, a 17β-hydroxysteroid dehydrogenase type 3 inhibitor, is efficacious in vivo in a novel hormone-dependent prostate cancer model
|
670
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Author's The development of steroid sulfatase inhibitors for hormone-dependent cancer therapy
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670
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Author's The In Vitro and In Vivo Activity of the Microtubule Disruptor STX140 Is Mediated by Hif-1 Alpha and CAIX Expression
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670
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Author's The in vivo properties of STX243: a potent angiogenesis inhibitor in breast cancer.
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670
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Author's The Regulation of Steroid Action by Sulfation and Desulfation
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670
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Author's The therapeutic potential of a series of orally bioavailable anti-angiogenic microtubule disruptors as therapy for hormone-independent prostate and breast cancers
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670
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Author's The use of steroid sulfatase inhibitors as a novel therapeutic strategy against hormone-dependent endometrial cancer
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909
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(orcid) 0000000171901592
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1
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919
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recentdevelopmentsofsteroidsulfataseinhibitorsasanticanceragents
‡A
Recent developments of steroid sulfatase inhibitors as anti-cancer agents.
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1
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919
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‡a
useofsteroidsulfataseinhibitorsasanoveltherapeuticstrategyagainsthormonedependentendometrialcancer
‡A
The use of steroid sulfatase inhibitors as a novel therapeutic strategy against hormone-dependent endometrial cancer
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1
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919
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‡a
therapeuticpotentialofaseriesoforallybioavailableantiangiogenicmicrotubuledisruptorsastherapyforhormoneindependentprostateandbreastcancers
‡A
The therapeutic potential of a series of orally bioavailable anti-angiogenic microtubule disruptors as therapy for hormone-independent prostate and breast cancers
‡9
1
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919
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‡a
regulationofsteroidactionbysulfationanddesulfation
‡A
The Regulation of Steroid Action by Sulfation and Desulfation
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1
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919
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‡a
invivopropertiesofstx243apotentangiogenesisinhibitorinbreastcancer
‡A
The in vivo properties of STX243: a potent angiogenesis inhibitor in breast cancer.
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1
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919
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‡a
invitroandinvivoactivityofthemicrotubuledisruptorstx140ismediatedbyhif1 Alpha andcaixexpression
‡A
The In Vitro and In Vivo Activity of the Microtubule Disruptor STX140 Is Mediated by Hif-1 Alpha and CAIX Expression
‡9
1
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919
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‡a
developmentofsteroidsulfataseinhibitorsforhormonedependentcancertherapy
‡A
The development of steroid sulfatase inhibitors for hormone-dependent cancer therapy
‡9
1
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919
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|
‡a
stx2171a17βhydroxysteroiddehydrogenasetype3inhibitorisefficaciousinvivoinanovelhormonedependentprostatecancermodel
‡A
STX2171, a 17β-hydroxysteroid dehydrogenase type 3 inhibitor, is efficacious in vivo in a novel hormone-dependent prostate cancer model
‡9
1
|
919
|
|
|
‡a
stx140isefficaciousinvitroandinvivointaxaneresistantbreastcarcinomacells
‡A
STX140 is efficacious in vitro and in vivo in taxane-resistant breast carcinoma cells.
‡9
1
|
919
|
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‡a
stx140butnotpaclitaxelinhibitsmammarytumourinitiationandprogressioninc31sv40ttantigentransgenicmice
‡A
STX140, but not paclitaxel, inhibits mammary tumour initiation and progression in C3(1)/SV40 T/t-antigen transgenic mice
‡9
1
|
919
|
|
|
‡a
structureactivityrelationshipsof10017cyanosubstitutedestratrienesasanticanceragents
‡A
Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents
‡9
1
|
919
|
|
|
‡a
steroidsulfataseinhibitorsforestrogenandandrogendependentcancers
‡A
Steroid sulfatase inhibitors for estrogen- and androgen-dependent cancers
‡9
1
|
919
|
|
|
‡a
17betahydroxysteroiddehydrogenasetype1andnottype12isatargetforendocrinetherapyofhormonedependentbreastcancer
‡A
17beta-hydroxysteroid dehydrogenase Type 1, and not Type 12, is a target for endocrine therapy of hormone-dependent breast cancer.
‡9
1
|
919
|
|
|
‡a
1hnmrmsbasedheterocovarianceasadrugdiscoverytoolforfishingbioactivecompoundsoutofacomplexmixtureofstructuralanalogues
‡A
1H NMR-MS-based heterocovariance as a drug discovery tool for fishing bioactive compounds out of a complex mixture of structural analogues
‡9
1
|
919
|
|
|
‡a
comparativestudyoftheabilityofcalcitoningenerelatedpeptideandadrenomedullin1352tomodulatemicrovascularbutnotthermalhyperalgesiaresponses
‡A
A comparative study of the ability of calcitonin gene-related peptide and adrenomedullin(13 - 52) to modulate microvascular but not thermal hyperalgesia responses
‡9
1
|
919
|
|
|
‡a
newmicronizedformulationof2methoxyestradiolbissulfamate
‡A
A new micronized formulation of 2-methoxyestradiol-bis-sulfamate
‡9
1
|
919
|
|
|
‡a
newmicronizedformulationof2methoxyestradiolbissulfamatestx140istherapeuticallypotentagainstbreastcancer
‡A
A new micronized formulation of 2-methoxyestradiol-bis-sulfamate (STX140) is therapeutically potent against breast cancer.
‡9
1
|
919
|
|
|
‡a
newtherapeuticstrategyagainsthormonedependentbreastcancerthepreclinicaldevelopmentofadualaromataseandsulfataseinhibitor
‡A
A new therapeutic strategy against hormone-dependent breast cancer: the preclinical development of a dual aromatase and sulfatase inhibitor
‡9
1
|
919
|
|
|
‡a
anticancersteroidsulfataseinhibitorssynthesisofapotentfluorinated2generationagentinvitroandinvivoactivitiesmolecularmodelingandproteincrystallography
‡A
Anticancer steroid sulfatase inhibitors: synthesis of a potent fluorinated second-generation agent, in vitro and in vivo activities, molecular modeling, and protein crystallography
‡9
1
|
919
|
|
|
‡a
antiinflammatoryactivityofsolubleguanylatecyclasecgmpdependentdownregulationofpselectinexpressionandleukocyterecruitment
‡A
Antiinflammatory activity of soluble guanylate cyclase: cGMP-dependent down-regulation of P-selectin expression and leukocyte recruitment.
‡9
1
|
919
|
|
|
‡a
bcrpexpressiondoesnotresultinresistancetostx140invivodespitetheincreasedexpressionofbcrpina2780cellsinvitroafterlongtermstx140exposure
‡A
BCRP expression does not result in resistance to STX140 in vivo, despite the increased expression of BCRP in A2780 cells in vitro after long-term STX140 exposure.
‡9
1
|
919
|
|
|
‡a
100typenatriureticpeptideinhibitsleukocyterecruitmentandplateletleukocyteinteractionsviasuppressionofpselectinexpression
‡A
C-type natriuretic peptide inhibits leukocyte recruitment and platelet-leukocyte interactions via suppression of P-selectin expression
‡9
1
|
919
|
|
|
‡a
chimericmicrotubuledisruptors
‡A
Chimeric microtubule disruptors
‡9
1
|
919
|
|
|
‡a
designsynthesisandbiologicalevaluationofnewarylamidederivativespossessingsulfonateorsulfamatemoietiesassteroidsulfataseenzymeinhibitors
‡A
Design, synthesis, and biological evaluation of new arylamide derivatives possessing sulfonate or sulfamate moieties as steroid sulfatase enzyme inhibitors
‡9
1
|
919
|
|
|
‡a
developmentofhormonedependentprostatecancermodelsfortheevaluationofinhibitorsof17betahydroxysteroiddehydrogenasetype3
‡A
Development of hormone-dependent prostate cancer models for the evaluation of inhibitors of 17beta-hydroxysteroid dehydrogenase type 3.
‡9
1
|
919
|
|
|
‡a
efficacyof3potentsteroidsulfataseinhibitorspreclinicalinvestigationsfortheiruseinthetreatmentofhormonedependentbreastcancer
‡A
Efficacy of three potent steroid sulfatase inhibitors: pre-clinical investigations for their use in the treatment of hormone-dependent breast cancer.
‡9
1
|
919
|
|
|
‡a
endothelialcellsplayanessentialroleinthethermalhyperalgesiainducedbynervegrowthfactor
‡A
Endothelial cells play an essential role in the thermal hyperalgesia induced by nerve growth factor.
‡9
1
|
919
|
|
|
‡a
estrogenactivationbysteroidsulfataseincreasescolorectalcancerproliferationviagper
‡A
Estrogen Activation by Steroid Sulfatase Increases Colorectal Cancer Proliferation via GPER.
‡9
1
|
919
|
|
|
‡a
estronesulfatetransportandsteroidsulfataseactivityincolorectalcancerimplicationsforhormonereplacementtherapy
‡A
Estrone Sulfate Transport and Steroid Sulfatase Activity in Colorectal Cancer: Implications for Hormone Replacement Therapy
‡9
1
|
919
|
|
|
‡a
intouchwithyourfemininesidehowoestrogenmetabolismimpactsprostatecancer
‡A
In touch with your feminine side: how oestrogen metabolism impacts prostate cancer
‡9
1
|
919
|
|
|
‡a
invivoandinvitropropertiesofstx2484anovelnonsteroidalanticancercompoundactiveintaxaneresistantbreastcancer
‡A
In vivo and in vitro properties of STX2484: a novel non-steroidal anti-cancer compound active in taxane-resistant breast cancer
‡9
1
|
919
|
|
|
‡a
invivoefficacyofstx213a2generationsteroidsulfataseinhibitorforhormonedependentbreastcancertherapy
‡A
In vivo efficacy of STX213, a second-generation steroid sulfatase inhibitor, for hormone-dependent breast cancer therapy.
‡9
1
|
919
|
|
|
‡a
invivoinhibitionofangiogenesisbysulphamoylatedderivativesof2methoxyoestradiol
‡A
In vivo inhibition of angiogenesis by sulphamoylated derivatives of 2-methoxyoestradiol
‡9
1
|
919
|
|
|
‡a
nntisakeyregulatorofadrenalredoxhomeostasisandsteroidogenesisinmalemice
‡A
NNT is a key regulator of adrenal redox homeostasis and steroidogenesis in male mice.
‡9
1
|
919
|
|
|
‡a
oestrogenandcolorectalcancermechanismsandcontroversies
‡A
Oestrogen and colorectal cancer: mechanisms and controversies
‡9
1
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946
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‡a
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|
|
|
‡2
ISNI|0000000117949560
|
996
|
|
|
‡2
RERO|A008677645
|
996
|
|
|
‡2
LC|nb 99101689
|
996
|
|
|
‡2
ISNI|0000000055138649
|
996
|
|
|
‡2
NTA|069105081
|
996
|
|
|
‡2
BNC|981060945028206706
|
996
|
|
|
‡2
NII|DA05331694
|
996
|
|
|
‡2
NKC|xx0203540
|
996
|
|
|
‡2
ISNI|0000000053337046
|
996
|
|
|
‡2
LC|no2017150841
|
996
|
|
|
‡2
DNB|103721028X
|
996
|
|
|
‡2
LC|no2002062541
|
996
|
|
|
‡2
ISNI|0000000507244347
|
996
|
|
|
‡2
LC|no2013036997
|
996
|
|
|
‡2
LC|n 2005073045
|
996
|
|
|
‡2
BAV|495_160806
|
996
|
|
|
‡2
NUKAT|n 2006002371
|
996
|
|
|
‡2
DNB|1089849729
|
996
|
|
|
‡2
DNB|128919205
|
996
|
|
|
‡2
NTA|069531544
|
996
|
|
|
‡2
SUDOC|251480119
|
996
|
|
|
‡2
LC|nb2021007447
|
996
|
|
|
‡2
SUDOC|078694566
|
997
|
|
|
‡a
0 0 lived 0 0
‡9
1
|