RIPOR3

gene
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Also known as dJ530I15.2dJ530I15.3

Summary

RIPOR3 (RIPOR family member 3, HGNC:16168) is a protein-coding gene on chromosome 20q13.13, encoding RIPOR family member 3 (Q96MK2).

At a glance

  • GWAS associations: 6
  • Clinical variants (ClinVar): 234 total
  • MANE Select transcript: NM_001290268

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:16168
Approved symbolRIPOR3
NameRIPOR family member 3
Location20q13.13
Locus typegene with protein product
StatusApproved
AliasesdJ530I15.2, dJ530I15.3
Ensembl geneENSG00000042062
Ensembl biotypeprotein_coding
Entrez140876

Gene structure

Transcript identifiers

Ensembl transcripts: 16 — 12 protein_coding, 3 protein_coding_CDS_not_defined, 1 retained_intron

ENST00000045083, ENST00000327979, ENST00000462493, ENST00000462842, ENST00000482129, ENST00000488529, ENST00000904041, ENST00000904042, ENST00000904043, ENST00000904044, ENST00000904045, ENST00000904046, ENST00000922749, ENST00000952574, ENST00000952575, ENST00000952576

RefSeq mRNA: 2 — MANE Select: NM_001290268 NM_001290268, NM_080829

CCDS: CCDS13431, CCDS93056

Canonical transcript exons

ENST00000327979 — 22 exons

ExonStartEnd
ENSE000010393095059758050597710
ENSE000015236695058610850587332
ENSE000015236715069112650691542
ENSE000015236765058968650589769
ENSE000015236785059455350594714
ENSE000034811415060861350608738
ENSE000035134335060464550604774
ENSE000035295965059303550593196
ENSE000035444235058780250587892
ENSE000035486455059614050596263
ENSE000035570415060929350609356
ENSE000035625165061600250616080
ENSE000036045925060207250602644
ENSE000036072045060891250608955
ENSE000036219825061085350610906
ENSE000036337915060838950608534
ENSE000036502065060957350609722
ENSE000036641515061998650620132
ENSE000036730645061118150611204
ENSE000036764355059234450592546
ENSE000036938105059536950595504
ENSE000038418715063073850630856

Expression profiles

Bgee: expression breadth ubiquitous, 190 present calls, max score 96.04.

FANTOM5 (CAGE): breadth broad, TPM avg 4.0573 / max 351.5298, expressed in 648 samples.

FANTOM5 promoters (12 alternative TSS)

Promoter IDTPM avgSamples expressed
1878731.6110115
1878770.9373368
1878740.568391
1878750.2484102
1878780.2304134
1878760.156476
1878790.080833
1878660.073917
1878680.049425
1878690.045425

Top tissues by expression

243 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
endocervixUBERON:000045896.04gold quality
metanephros cortexUBERON:001053395.90gold quality
left uterine tubeUBERON:000130395.57gold quality
body of uterusUBERON:000985394.46gold quality
apex of heartUBERON:000209893.73gold quality
oocyteCL:000002392.69gold quality
omental fat padUBERON:001041491.99gold quality
mucosa of stomachUBERON:000119991.93gold quality
peritoneumUBERON:000235891.88gold quality
ectocervixUBERON:001224991.80gold quality
adipose tissue of abdominal regionUBERON:000780890.84gold quality
kidney epitheliumUBERON:000481989.81gold quality
uterine cervixUBERON:000000289.57gold quality
right adrenal gland cortexUBERON:003582789.45gold quality
heart left ventricleUBERON:000208489.02gold quality
cardiac ventricleUBERON:000208288.63gold quality
right adrenal glandUBERON:000123388.55gold quality
adrenal cortexUBERON:000123588.50gold quality
left adrenal gland cortexUBERON:003582588.16gold quality
right lobe of liverUBERON:000111488.03gold quality
subcutaneous adipose tissueUBERON:000219087.69gold quality
lower esophagus muscularis layerUBERON:003583387.65gold quality
lower esophagusUBERON:001347387.59gold quality
left adrenal glandUBERON:000123487.45gold quality
right ovaryUBERON:000211887.29gold quality
small intestine Peyer’s patchUBERON:000345486.99gold quality
secondary oocyteCL:000065586.90gold quality
right uterine tubeUBERON:000130286.87gold quality
vaginaUBERON:000099686.69gold quality
adrenal glandUBERON:000236986.65gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-GEOD-75367yes1931.33
E-ANND-3yes12.54

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

36 targeting RIPOR3, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-499A-5P99.9870.791323
HSA-MIR-205-3P99.9269.923165
HSA-MIR-808799.9069.551351
HSA-MIR-449699.8868.892236
HSA-MIR-3140-3P99.8868.472069
HSA-MIR-449299.8768.253611
HSA-MIR-3065-3P99.8770.251407
HSA-MIR-6817-3P99.7968.352126
HSA-MIR-808499.7369.571760
HSA-MIR-6762-3P99.6666.941188
HSA-MIR-360999.5269.892587
HSA-MIR-548AH-5P99.5269.732626
HSA-MIR-1912-3P99.3267.40936
HSA-MIR-122B-3P99.2168.901333
HSA-MIR-21-3P99.2168.951312
HSA-MIR-6852-5P99.1766.692073
HSA-MIR-6815-3P99.1368.981530
HSA-MIR-425499.1165.151315
HSA-MIR-6738-3P99.0367.141326
HSA-MIR-939-3P98.9765.072347
HSA-MIR-392698.9569.261438
HSA-MIR-5001-3P98.9167.281394
HSA-MIR-465698.7966.221306
HSA-MIR-19898.7067.32920
HSA-MIR-471898.5568.61814
HSA-MIR-3187-5P98.3665.741776
HSA-MIR-3664-3P97.8567.621452
HSA-MIR-1285-3P97.7267.021932
HSA-MIR-5189-5P97.7266.961814
HSA-MIR-686097.2166.311656

Literature-anchored findings (GeneRIF, showing 1)

  • Downregulated Expression of RIPOR3 Correlated with Immune Infiltrates Predicts Poor Prognosis in Oral Tongue Cancer. (PMID:35277469)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_rerioripor3ENSDARG00000020979
mus_musculusRipor3ENSMUSG00000074577
rattus_norvegicusRipor3ENSRNOG00000010791
caenorhabditis_elegansWBGENE00045063

Paralogs (2): RIPOR1 (ENSG00000039523), RIPOR2 (ENSG00000111913)

Protein

Protein identifiers

RIPOR family member 3Q96MK2 (reviewed: Q96MK2)

All UniProt accessions (2): A0A499FJE4, Q96MK2

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the RIPOR family.

Isoforms (2)

UniProt IDNamesCanonical?
Q96MK2-11yes
Q96MK2-22

RefSeq proteins (2): NP_001277197, NP_543019 (=MANE)

Domains & families (InterPro)

IDNameType
IPR026136RIPOR3Family
IPR031780FAM65_NDomain

Pfam: PF15903

UniProt features (16 total): modified residue 6, compositionally biased region 3, sequence variant 2, sequence conflict 2, chain 1, region of interest 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96MK2-F169.660.24

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (6): 384, 9, 24, 340, 345, 351

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 67 (showing top): WONG_ENDMETRIUM_CANCER_DN, MODULE_301, SCHAEFFER_PROSTATE_DEVELOPMENT_48HR_UP, CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_5, CERVERA_SDHB_TARGETS_1_UP, CHARAFE_BREAST_CANCER_LUMINAL_VS_MESENCHYMAL_UP, MASSARWEH_TAMOXIFEN_RESISTANCE_UP, NIKOLSKY_BREAST_CANCER_20Q12_Q13_AMPLICON, CHEN_METABOLIC_SYNDROM_NETWORK, STAMBOLSKY_TARGETS_OF_MUTATED_TP53_DN, DUTERTRE_ESTRADIOL_RESPONSE_24HR_DN, EIF4E_UP, CHARAFE_BREAST_CANCER_LUMINAL_VS_BASAL_UP, CBX5_TARGET_GENES, FOXN3_TARGET_GENES

GO Biological Process (0):

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (0):

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1

Protein interactions and networks

STRING

928 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
RIPOR3HSD17B13Q7Z5P4447
RIPOR3SUSD1Q6UWL2422
RIPOR3EFCAB5A4FU69410
RIPOR3LTC4SQ16873410
RIPOR3ERICH6Q7L0X2404
RIPOR3TRAPPC13A5PLN9381
RIPOR3VSIG8P0DPA2377
RIPOR3ANKIB1Q9P2G1377
RIPOR3NSRP1Q9H0G5376
RIPOR3PBDC1Q9BVG4374
RIPOR3TAGAPQ8N103366
RIPOR3AADACL3Q5VUY0365
RIPOR3DPH6Q7L8W6351
RIPOR3TMPRSS11EQ9UL52349
RIPOR3TMEM72A0PK05345

IntAct

20 interactions, top by confidence:

ABTypeScore
RHOARIPOR3psi-mi:“MI:0915”(physical association)0.670
RIPOR3SHANK2psi-mi:“MI:0915”(physical association)0.560
CCDC125RIPOR3psi-mi:“MI:0915”(physical association)0.560
TRAF1RIPOR3psi-mi:“MI:0915”(physical association)0.560
RHOCRIPOR3psi-mi:“MI:0915”(physical association)0.560
SCML4RIPOR3psi-mi:“MI:0915”(physical association)0.560
RIPOR3AIPpsi-mi:“MI:0914”(association)0.350
RIPOR3RHOCpsi-mi:“MI:0915”(physical association)0.000
RIPOR3SHANK2psi-mi:“MI:0915”(physical association)0.000
RIPOR3CCDC125psi-mi:“MI:0915”(physical association)0.000
RIPOR3TRAF1psi-mi:“MI:0915”(physical association)0.000
RHOARIPOR3psi-mi:“MI:0915”(physical association)0.000
RIPOR3SCML4psi-mi:“MI:0915”(physical association)0.000

BioGRID (11): TRAF1 (Two-hybrid), RHOA (Two-hybrid), SCML4 (Two-hybrid), RHOC (Two-hybrid), SHANK2 (Two-hybrid), CCDC125 (Two-hybrid), SLC9A3R2 (Affinity Capture-MS), SLC9A3R1 (Affinity Capture-MS), SRPK3 (Affinity Capture-MS), AIP (Affinity Capture-MS), RHOA (Affinity Capture-MS)

ESM2 similar proteins: A0JNQ6, A6NC42, A6NGQ2, A6NGR9, A6QP75, A7E3N7, A9X185, E1BDF2, E9PGG2, F6SZT2, P0C7A0, P85965, Q06VW1, Q0ZFW8, Q14DK4, Q3UK37, Q3UV16, Q3ZBN4, Q400G9, Q4VXA5, Q587J8, Q5JSQ8, Q60953, Q60I26, Q60I27, Q6NUI2, Q6ZUX3, Q810I0, Q8BH06, Q8C0R7, Q8IWB1, Q8IWY9, Q8IYX4, Q8K4C2, Q8N6L0, Q8N7F7, Q8NCV1, Q8TE82, Q91WA6, Q95JV3

Diamond homologs: A1L3T7, A9ZLX4, Q1LU99, Q3B7M3, Q4FZU8, Q5EB20, Q5F3L9, Q68FE6, Q6ZS17, Q7TP54, Q80U16, Q96MK2, Q9Y4F9, O46119, O46414, O46415, O65100, P02791, P02792, P02793, P02794, P07229, P07797, P07798, P08267, P09451, P09528, P0C7X4, P17663, P18685, P18686, P19130, P19132, P19133, P19975, P19976, P25319, P25320, P25699, P25915

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

234 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance200
Likely benign17
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

5350 predictions. Top by Δscore:

VariantEffectΔscore
20:50589680:GCTCA:Gdonor_loss1.0000
20:50589681:CTCA:Cdonor_loss1.0000
20:50589682:TCA:Tdonor_loss1.0000
20:50589683:CACCT:Cdonor_loss1.0000
20:50589684:A:Tdonor_loss1.0000
20:50589685:C:CAdonor_loss1.0000
20:50592339:CGTA:Cdonor_loss1.0000
20:50592340:GTA:Gdonor_loss1.0000
20:50592343:C:Adonor_loss1.0000
20:50592542:TGTCA:Tacceptor_gain1.0000
20:50592543:GTCA:Gacceptor_gain1.0000
20:50592544:TCA:Tacceptor_gain1.0000
20:50592545:CA:Cacceptor_gain1.0000
20:50592545:CAC:Cacceptor_gain1.0000
20:50592546:ACT:Aacceptor_loss1.0000
20:50592547:C:CCacceptor_gain1.0000
20:50592547:CTAG:Cacceptor_loss1.0000
20:50592548:T:Gacceptor_loss1.0000
20:50593030:CTTA:Cdonor_loss1.0000
20:50593031:TTA:Tdonor_loss1.0000
20:50593032:TACCT:Tdonor_loss1.0000
20:50593033:ACC:Adonor_loss1.0000
20:50593033:ACCTT:Adonor_gain1.0000
20:50593034:CCTT:Cdonor_gain1.0000
20:50593034:CCTTC:Cdonor_gain1.0000
20:50593037:T:Adonor_gain1.0000
20:50593193:CACG:Cacceptor_gain1.0000
20:50593195:CG:Cacceptor_gain1.0000
20:50593197:C:CCacceptor_gain1.0000
20:50593202:C:CTacceptor_gain1.0000

AlphaMissense

6148 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
20:50608393:A:GW314R0.998
20:50608393:A:TW314R0.998
20:50608410:A:GL308P0.998
20:50608669:A:GW248R0.998
20:50608669:A:TW248R0.998
20:50608404:A:GL310P0.996
20:50608952:A:GL211S0.996
20:50610865:A:CF134L0.996
20:50610865:A:TF134L0.996
20:50610867:A:GF134L0.996
20:50608391:C:AW314C0.995
20:50608391:C:GW314C0.995
20:50608412:C:AK307N0.995
20:50608412:C:GK307N0.995
20:50608667:C:AW248C0.995
20:50608667:C:GW248C0.995
20:50608711:A:GW234R0.995
20:50608711:A:TW234R0.995
20:50608392:C:GW314S0.994
20:50608414:T:CK307E0.993
20:50608699:C:GG238R0.993
20:50608917:A:CY223D0.993
20:50608934:A:GL217P0.993
20:50608410:A:TL308Q0.992
20:50608698:C:TG238D0.992
20:50619989:A:GL85P0.992
20:50608922:T:AD221V0.991
20:50608922:T:GD221A0.991
20:50610878:C:GR130P0.991
20:50608410:A:CL308R0.990

dbSNP variants (sampled 300 via entrez): RS1000036390 (20:50612329 C>G,T), RS1000077916 (20:50614377 G>A), RS1000078272 (20:50601870 A>T), RS1000160007 (20:50641228 G>A,T), RS1000173448 (20:50666522 C>A), RS1000184305 (20:50646032 C>G,T), RS1000198466 (20:50651803 G>A,T), RS1000205538 (20:50627760 G>A), RS1000267970 (20:50657490 G>A), RS1000326649 (20:50692294 G>A,C), RS1000371848 (20:50633555 T>G), RS1000376050 (20:50686388 G>A), RS1000409345 (20:50686447 A>C,G), RS1000436654 (20:50692050 T>A,C), RS1000470571 (20:50638650 G>C,T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (1): prostate cancer (MONDO:0008315)

Orphanet (1): Familial prostate cancer (Orphanet:1331)

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

6 associations (top):

StudyTraitp-value
GCST009391_152Metabolite levels1.000000e-06
GCST010083_104Hemoglobin levels1.000000e-08
GCST012490_639Femur bone mineral density x serum urate levels interaction4.000000e-09
GCST90002388_582Lymphocyte count4.000000e-19
GCST90002401_325Platelet distribution width2.000000e-10
GCST90002407_176White blood cell count2.000000e-14

EFO canonical traits (5, from GWAS)

EFO IDTrait name
EFO:0010486glucuronate measurement
EFO:0004509hemoglobin measurement
EFO:0004531urate measurement
EFO:0004587lymphocyte count
EFO:0007984platelet component distribution width

MeSH disease descriptors (1)

DescriptorNameTree numbers
D011471Prostatic NeoplasmsC04.588.945.440.770; C12.100.500.260.750; C12.100.500.565.625; C12.200.294.260.750; C12.200.294.565.625; C12.200.758.409.750; C12.900.619.750

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

27 total (human), top 27 by PubMed support.

ChemicalActions (top 5)PubMed papers
methylmercuric chloridedecreases expression2
bisphenol Adecreases expression, decreases methylation2
Calcitrioldecreases expression, increases expression2
Aflatoxin B1decreases methylation, increases methylation2
aristolochic acid Iincreases expression1
2,5,2’,5’-tetrachlorobiphenyldecreases expression1
aflatoxin B2increases methylation1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression, affects cotreatment, decreases expression1
licochalcone Bincreases expression1
bisphenol Sdecreases expression1
bisphenol AFdecreases expression1
2,3,5-trichloro-6-phenyl-(1,4)benzoquinonedecreases expression1
Zoledronic Aciddecreases expression1
Leflunomideincreases expression1
Atrazineincreases expression1
Benzo(a)pyreneaffects expression1
Dexamethasoneincreases expression1
Lipopolysaccharidesdecreases expression, affects response to substance, increases expression, affects cotreatment1
Nickelincreases expression1
Oxygenaffects expression1
Smokeincreases expression1
Tetrachlorodibenzodioxinincreases expression1
Tobacco Smoke Pollutiondecreases expression1
Valproic Acidaffects expression1
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxideincreases expression1
Okadaic Aciddecreases expression1
Lactic Aciddecreases expression1

Clinical trials (associated diseases)

300 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT00029224PHASE4COMPLETEDTreatment With Zoledronic Acid in Patients With Breast Cancer, Multiple Myeloma, and Prostate Cancer With Cancer Related Bone Lesions
NCT00035997PHASE4COMPLETEDOpen-label Trial on the Effect of I.V. Zoledronic Acid 4 mg on Bone Density in Hormone Sensitive Prostate Cancer Patients With Bone Metastasis
NCT00063609PHASE4COMPLETEDThe Effect of Zoledronic Acid on Bone Loss in Prostate Cancer Patients Undergoing Androgen Deprivation Therapy
NCT00103623PHASE4SUSPENDEDThe Plenaxis® Experience Study
NCT00106392PHASE4COMPLETEDA Safety and Efficacy Study of Prograf in the Prevention of Erectile Dysfunction After Radical Prostatectomy
NCT00185029PHASE4UNKNOWNMR-Lymphography and Lymph Node Staging in Prostate Cancer
NCT00199485PHASE4COMPLETEDAngelica Sinensis for the Treatment of Hot Flashes in Men Undergoing LHRH Therapy for Prostate Cancer
NCT00219219PHASE4COMPLETEDZoledronic Acid in the Prevention of Skeletal-related Events in Hormone Refractory and Hormone-sensitive Prostate Cancer Patients With Bone Metastases
NCT00219271PHASE4COMPLETEDEffect Of Zoledronic Acid On Circulating And Bone Marrow-Residing Prostate Cancer Cells In Patients With Clinically Localized Prostate Cancer
NCT00237146PHASE4COMPLETEDStudy to Evaluate Zoledronic Acid on Quality of Life and Skeletal-related Events as Adjuvant Treatment in Patients With Hormone-naïve Prostate Cancer and Bone Metastasis Who Have Undergone Orchiectomy
NCT00242554PHASE4COMPLETEDOpen-label Phase IV Clinical Trial to Evaluate the Safety and Tolerability of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastases
NCT00280098PHASE4COMPLETEDDocetaxel in the Treatment of Hormone Refractory Prostate Cancer
NCT00293696PHASE4COMPLETEDCasodex/Zoladex Biomarkers in Localised Prostate Cancer
NCT00334139PHASE4COMPLETEDEffect of Zoledronic Acid on Bone Metabolism in Patients With Bone Metastasis and Prostate or Breast Cancer
NCT00375765PHASE4COMPLETEDEffects On Dihydrotestosterone Regulated Gene Expression In Benign Prostatic Hyperplasia Or Prostate Cancer
NCT00391690PHASE4COMPLETEDEvaluation of Bone Markers as Diagnostic Tools for Early Detection of Bone Metastases in Patients With High Risk Prostate Cancer
NCT00422708PHASE4COMPLETEDLocal Anesthesia for Prostate Biopsy
NCT00526331PHASE4COMPLETEDEvaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy
NCT00590213PHASE4COMPLETEDCompare the Value of Prophylactic Versus Therapeutic Breast Radiotherapy in CASODEX
NCT00629330PHASE4TERMINATEDDissemination of Prostate Cancer Screening to PCP’s in African American Communities
NCT00771966PHASE4COMPLETEDRadical Prostatectomy and Perioperative Fluid Therapy
NCT00805701PHASE4COMPLETEDStudy Assessing The Efficacy And Safety Of Avodart (Dutasteride) At Improving Urinary Symptoms In Men With Prostate Cancer Who Are Undergoing Seed Implantation
NCT00859027PHASE4COMPLETEDEffect Of Risedronate On Bone Mass In Older Men Receiving Neoadjuvant Therapy For Prostate Cancer
NCT00906269PHASE4UNKNOWNCan Hyperbaric Oxygen Improve Erectile Function Following Surgery for Prostate Cancer
NCT00953277PHASE4COMPLETEDStudy of Nerve Reconstruction Using AVANCE in Subjects Who Undergo Robotic Assisted Prostatectomy for Treatment of Prostate Cancer
NCT00982800PHASE4COMPLETEDDoes Postoperative Gabapentin Reduce Pain, Opioid Consumption and Anxiety and Have a Positive Effect on Health Related Quality of Life After Radical Prostatectomy?
NCT01083199PHASE4COMPLETEDGlobal Performance Evaluation of the AMS CONTINUUM™ Device
NCT01136226PHASE4COMPLETEDEvaluate Recovery of Testosterone for Patients Using Eligard
NCT01161563PHASE4COMPLETEDRandomized Crossover Trial to Assess the Tolerability of Gonadotropin Releasing Hormone (GnRH) Analogue Administration
NCT01230905PHASE4COMPLETEDStudy to Monitor the Effects of Androgen Suppression Treatment on the Heart
NCT01296672PHASE4COMPLETED3 Month Finasteride Challenge Test Can Significantly Improve the Performance of Screening for Prostate Cancer
NCT01365143PHASE4TERMINATEDProspective Randomized Trial Comparing Robotic Versus Open Radical Prostatectomy
NCT01379742PHASE4UNKNOWNComparison of Between ThinSeed™ and OncoSeed™ for Permanent Prostate Brachytherapy
NCT01486563PHASE4COMPLETEDHydroxyethyl Starch and Renal Function After Radical Prostatectomy
NCT01511874PHASE4COMPLETEDEfficacy and Safety Study of ELIGARD 22.5mg With Prostate Cancer
NCT01512472PHASE4TERMINATEDFirmagon (Degarelix) Intermittent Therapy
NCT01547416PHASE4COMPLETEDThe Effect of Combined General/Epidural Anesthesia Versus General Anesthesia on Diaphragmatic Function
NCT01571544PHASE4COMPLETEDThe Use of Thermal Suits as Preventing Hypothermia During Surgery
NCT01581749PHASE4UNKNOWNEvaluation of Truebeam for Low-Intermediate Risk Prostate Cancer
NCT01649635PHASE4COMPLETEDStudy of Cabazitaxel Combined With Prednisone and Prophylaxis of Neutropenia Complications in the Treatment of Patients With Metastatic Castration-resistant Prostate Cancer

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.