DHDH

gene
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Also known as HUM2DD

Summary

DHDH (dihydrodiol dehydrogenase, HGNC:17887) is a protein-coding gene on chromosome 19q13.33, encoding Trans-1,2-dihydrobenzene-1,2-diol dehydrogenase (Q9UQ10).

This gene encodes an enzyme that belongs to the family of dihydrodiol dehydrogenases, which exist in multiple forms in mammalian tissues and are involved in the metabolism of xenobiotics and sugars. These enzymes catalyze the NADP1-linked oxidation of transdihydrodiols of aromatic hydrocarbons to corresponding catechols. This enzyme is a dimeric dihydrodiol dehydrogenase, and it differs from monomeric dihydrodiol dehydrogenases in its high substrate specificity for trans-dihydrodiols of aromatic hydrocarbons in the oxidative direction.

Source: NCBI Gene 27294 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 79 total
  • MANE Select transcript: NM_014475

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:17887
Approved symbolDHDH
Namedihydrodiol dehydrogenase
Location19q13.33
Locus typegene with protein product
StatusApproved
AliasesHUM2DD
Ensembl geneENSG00000104808
Ensembl biotypeprotein_coding
OMIM606377
Entrez27294

Gene structure

Transcript identifiers

Ensembl transcripts: 4 — 3 protein_coding, 1 nonsense_mediated_decay

ENST00000221403, ENST00000520557, ENST00000522614, ENST00000523250

RefSeq mRNA: 1 — MANE Select: NM_014475 NM_014475

CCDS: CCDS12741

Canonical transcript exons

ENST00000221403 — 7 exons

ExonStartEnd
ENSE000007185064893500048935111
ENSE000007185134893603248936195
ENSE000007185274894244048942564
ENSE000012296784894482448944969
ENSE000012296844893369948933811
ENSE000035330864894435748944507
ENSE000035441964893944948939701

Expression profiles

Bgee: expression breadth ubiquitous, 156 present calls, max score 90.85.

FANTOM5 (CAGE): breadth broad, TPM avg 1.0548 / max 74.2322, expressed in 420 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1768831.0548420

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
kidney epitheliumUBERON:000481990.85gold quality
ileal mucosaUBERON:000033189.41gold quality
jejunal mucosaUBERON:000039989.17gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047388.05gold quality
duodenumUBERON:000211487.84gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099179.87gold quality
adult mammalian kidneyUBERON:000008279.38gold quality
jejunumUBERON:000211578.04gold quality
kidneyUBERON:000211375.72gold quality
spermCL:000001973.94gold quality
small intestineUBERON:000210873.05gold quality
small intestine Peyer’s patchUBERON:000345471.78gold quality
amniotic fluidUBERON:000017371.76silver quality
cortex of kidneyUBERON:000122570.67gold quality
buccal mucosa cellCL:000233669.67gold quality
prefrontal cortexUBERON:000045169.61gold quality
cerebellar hemisphereUBERON:000224569.42gold quality
renal medullaUBERON:000036269.37gold quality
cerebellar cortexUBERON:000212969.29gold quality
cerebellumUBERON:000203768.78gold quality
right hemisphere of cerebellumUBERON:001489067.96gold quality
cardia of stomachUBERON:000116267.47gold quality
spleenUBERON:000210667.04gold quality
Brodmann (1909) area 9UBERON:001354066.85gold quality
epithelial cell of pancreasCL:000008366.81gold quality
nucleus accumbensUBERON:000188266.67gold quality
right frontal lobeUBERON:000281066.55gold quality
pituitary glandUBERON:000000766.35gold quality
frontal cortexUBERON:000187066.35gold quality
vena cavaUBERON:000408766.16gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes3.07

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 5)

  • Site-directed mutagenesis of conserved residues shows that Tyr-180 plays a critical role in the catalytic function of this enzyme, while His-79 is required in the coenzyme binding and chemical steps of the reaction. (PMID:11097839)
  • Comparison of other mammalian homologs with the human enzyme shows that dimeric DDs constitute a novel protein family. (PMID:11306093)
  • Survival was significantly better in gastric cancer patients with low DDH expression. (PMID:18600452)
  • Possible association of both variants of the DHDH gene with familial Dupuytren’s disease, as over-representation of the rs2270941 and rs11666105 alterations was identified among 100 patients with a familial history. (PMID:23303836)
  • Some genetical studies show also altered expression of the dehydrogenases ALDH2 and DHDH genes in patients with Dupuytren’s disease and with digestive tract malignancies related to alcohol abuse.(review) (PMID:24734329)

Cross-species orthologs

7 orthologs

OrganismSymbolGene ID
danio_reriodhdh.2ENSDARG00000019081
danio_reriodhdh.1ENSDARG00000028336
mus_musculusDhdhENSMUSG00000011382
rattus_norvegicusDhdhENSRNOG00000020883
drosophila_melanogasterCG3597FBGN0031417
drosophila_melanogasterCG3609FBGN0031418
drosophila_melanogasterCG13280FBGN0032609

Paralogs (3): BLVRA (ENSG00000106605), GFOD2 (ENSG00000141098), GFOD1 (ENSG00000145990)

Protein

Protein identifiers

Trans-1,2-dihydrobenzene-1,2-diol dehydrogenaseQ9UQ10 (reviewed: Q9UQ10)

Alternative names: D-xylose 1-dehydrogenase, D-xylose-NADP dehydrogenase, Dimeric dihydrodiol dehydrogenase, Hum2DD

All UniProt accessions (4): E5RFE0, E5RGT8, Q9UQ10, H0YBU7

UniProt curated annotations — full annotation on UniProt →

Subunit / interactions. Homodimer.

Tissue specificity. Small intestine.

Similarity. Belongs to the Gfo/Idh/MocA family.

RefSeq proteins (1): NP_055290* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000683Gfo/Idh/MocA-like_OxRdtase_NDomain
IPR036291NAD(P)-bd_dom_sfHomologous_superfamily
IPR050984Gfo/Idh/MocA_domainFamily
IPR055170GFO_IDH_MocA-like_domDomain

Pfam: PF01408, PF22725

Catalyzed reactions (Rhea), 2 shown:

  • (1R,2R)-1,2-dihydrobenzene-1,2-diol + NADP(+) = catechol + NADPH + H(+) (RHEA:16729)
  • D-xylose + NADP(+) = D-xylono-1,5-lactone + NADPH + H(+) (RHEA:22000)

UniProt features (11 total): site 5, sequence variant 5, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9UQ10-F198.190.99

Functional residue map

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

Catalytic / active sites (5): 71 (may play an important role in coenzyme binding); 79 (may play an important role in coenzyme binding); 97 (may play an important role in coenzyme binding); 176 (may play an important role for the adaptation of the alcohol substrate into the binding site); 180 (may play an important role in catalytic activity)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 55 (showing top): GOMF_OXIDOREDUCTASE_ACTIVITY_ACTING_ON_THE_CH_CH_GROUP_OF_DONORS, GOBP_MONOSACCHARIDE_CATABOLIC_PROCESS, GOBP_CARBOHYDRATE_METABOLIC_PROCESS, GOBP_SMALL_MOLECULE_CATABOLIC_PROCESS, GOBP_CARBOHYDRATE_CATABOLIC_PROCESS, GOMF_OXIDOREDUCTASE_ACTIVITY_ACTING_ON_CH_OH_GROUP_OF_DONORS, GOBP_MONOSACCHARIDE_METABOLIC_PROCESS, GOBP_PENTOSE_METABOLIC_PROCESS, KEGG_METABOLISM_OF_XENOBIOTICS_BY_CYTOCHROME_P450, GOMF_OXIDOREDUCTASE_ACTIVITY_ACTING_ON_THE_CH_CH_GROUP_OF_DONORS_NAD_OR_NADP_AS_ACCEPTOR, KEGG_PENTOSE_AND_GLUCURONATE_INTERCONVERSIONS, MIKKELSEN_MEF_HCP_WITH_H3_UNMETHYLATED, ANDERSEN_CHOLANGIOCARCINOMA_CLASS2, ARNT2_TARGET_GENES, ATF6_TARGET_GENES

GO Biological Process (1): D-xylose catabolic process (GO:0042843)

GO Molecular Function (4): nucleotide binding (GO:0000166), trans-1,2-dihydrobenzene-1,2-diol dehydrogenase activity (GO:0047115), D-xylose 1-dehydrogenase (NADP+) activity (GO:0047837), oxidoreductase activity (GO:0016491)

GO Cellular Component (0):

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
pentose catabolic process1
D-xylose metabolic process1
nucleoside phosphate binding1
heterocyclic compound binding1
oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor1
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor1
catalytic activity1

Protein interactions and networks

STRING

1365 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
DHDHAKR1C4P17516925
DHDHAKR1C1P52896913
DHDHAKR1C2P52895907
DHDHAKR1C3P42330899
DHDHDHRS9Q9BPW9834
DHDHH2BC21Q16778722
DHDHB2MP01884576
DHDHKLRD1Q13241576
DHDHENPEPQ07075550
DHDHCD8AP01732540
DHDHITIH4Q14624529
DHDHCD300AQ9UGN4473
DHDHCD300LFQ8TDQ1472
DHDHAKR1A1P14550464
DHDHDDX53Q86TM3450

IntAct

3 interactions, top by confidence:

ABTypeScore
DHDHATRNpsi-mi:“MI:0914”(association)0.530
DHDHZNF185psi-mi:“MI:0914”(association)0.350

BioGRID (46): CCDC12 (Affinity Capture-MS), TSC22D1 (Affinity Capture-MS), CBWD3 (Affinity Capture-MS), NFXL1 (Affinity Capture-MS), TUBB (Affinity Capture-MS), AP3M2 (Affinity Capture-MS), TUBA1C (Affinity Capture-MS), CDC42EP1 (Affinity Capture-MS), ICAM1 (Affinity Capture-MS), CCP110 (Affinity Capture-MS), CCDC47 (Affinity Capture-MS), MADD (Affinity Capture-MS), FAM91A1 (Affinity Capture-MS), ARHGEF4 (Affinity Capture-MS), HK2 (Affinity Capture-MS)

ESM2 similar proteins: D3ZDK7, E9Q3E1, O93539, O93541, O93542, O93543, O93545, O93546, P00325, P00328, P13439, P31754, P33571, P42122, P43353, P69080, P69081, P69082, P69085, P69086, P70473, P80338, P81600, P97849, Q08415, Q148L6, Q16773, Q1JPA0, Q3TY86, Q5R1W2, Q5R5J5, Q5RDY4, Q5TEU4, Q60714, Q642M9, Q64674, Q6DF30, Q6DKE0, Q6P1M0, Q7JK39

Diamond homologs: A0A024SMV2, A0R191, A4FDY3, A6WFC5, A9N564, B3TMR8, B5F3F4, C0ZWI9, D4GP30, F0M433, O13991, O32223, O42896, P40332, P46853, P49307, P77376, Q148L6, Q44258, Q54728, Q5R5J5, Q642M9, Q6DF30, Q6DKE0, Q7CV90, Q7JK39, Q88S38, Q8ZK57, Q92KZ3, Q9ALN5, Q9DBB8, Q9TQS6, Q9TV68, Q9TV69, Q9TV70, Q9UQ10, Q9UT60, Q9ZA33, A0A0F7VN41, A0JT53

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance62
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

862 predictions. Top by Δscore:

VariantEffectΔscore
19:48933807:ACCAG:Adonor_loss1.0000
19:48933808:CCAGG:Cdonor_loss1.0000
19:48933809:CAGGT:Cdonor_loss1.0000
19:48933811:GG:Gdonor_loss1.0000
19:48933812:G:Tdonor_loss1.0000
19:48933837:G:GTdonor_gain1.0000
19:48933837:G:Tdonor_gain1.0000
19:48934995:TCCA:Tacceptor_loss1.0000
19:48934998:A:ACacceptor_loss1.0000
19:48934998:A:AGacceptor_gain1.0000
19:48934998:AG:Aacceptor_gain1.0000
19:48934998:AGGT:Aacceptor_gain1.0000
19:48934998:AGGTG:Aacceptor_gain1.0000
19:48934999:G:Aacceptor_loss1.0000
19:48934999:G:GTacceptor_gain1.0000
19:48934999:GG:Gacceptor_gain1.0000
19:48934999:GGT:Gacceptor_gain1.0000
19:48934999:GGTG:Gacceptor_gain1.0000
19:48934999:GGTGG:Gacceptor_gain1.0000
19:48935108:GTGG:Gdonor_gain1.0000
19:48935109:TGG:Tdonor_gain1.0000
19:48935110:GG:Gdonor_gain1.0000
19:48935110:GGG:Gdonor_gain1.0000
19:48935110:GGGT:Gdonor_loss1.0000
19:48935111:GG:Gdonor_gain1.0000
19:48935111:GGTG:Gdonor_loss1.0000
19:48935112:G:GGdonor_gain1.0000
19:48935113:T:Adonor_loss1.0000
19:48936027:CCTA:Cacceptor_loss1.0000
19:48936028:CTA:Cacceptor_loss1.0000

AlphaMissense

2171 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:48942505:A:CS229R0.984
19:48942507:C:AS229R0.984
19:48942507:C:GS229R0.984
19:48936116:A:TE96V0.982
19:48935042:T:CF45L0.978
19:48935044:T:AF45L0.978
19:48935044:T:GF45L0.978
19:48944835:A:CS303R0.975
19:48944837:T:AS303R0.975
19:48944837:T:GS303R0.975
19:48933734:T:AW5R0.971
19:48933734:T:CW5R0.971
19:48944447:T:CF279L0.967
19:48944449:T:AF279L0.967
19:48944449:T:GF279L0.967
19:48939542:T:CF154L0.966
19:48939544:T:AF154L0.966
19:48939544:T:GF154L0.966
19:48933770:T:CF17L0.965
19:48933772:C:AF17L0.965
19:48933772:C:GF17L0.965
19:48944476:G:CE288D0.965
19:48944476:G:TE288D0.965
19:48933736:G:CW5C0.956
19:48933736:G:TW5C0.956
19:48936117:G:CE96D0.954
19:48936117:G:TE96D0.954
19:48944414:T:CF268L0.950
19:48944416:C:AF268L0.950
19:48944416:C:GF268L0.950

dbSNP variants (sampled 300 via entrez): RS1000022331 (19:48932310 G>A), RS1000038394 (19:48940592 G>A), RS1000087336 (19:48940750 G>A), RS1000909338 (19:48935756 G>A), RS1001552289 (19:48941422 C>T), RS1001660744 (19:48936770 G>A), RS1001793559 (19:48945397 G>A,C), RS1001818986 (19:48931069 T>G), RS1002159577 (19:48939954 G>A), RS1002255275 (19:48945163 A>G), RS1002360808 (19:48935539 C>T), RS1002412360 (19:48945322 GAAA>G,GAA,GAAAA), RS1002675524 (19:48940424 T>A), RS1002702788 (19:48934126 G>A), RS1002763753 (19:48935257 C>T)

Disease associations

OMIM: gene MIM:606377 | 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

0 associations (top):

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
Benzo(a)pyrenedecreases methylation, increases expression2
Silicon Dioxideincreases expression2
Tobacco Smoke Pollutionincreases expression2
Cadmium Chloridedecreases expression, increases expression2
aristolochic acid Iincreases expression1
propionaldehydeincreases expression1
mesityleneincreases expression1
tris(2-butoxyethyl) phosphateaffects expression1
tris(1,3-dichloro-2-propyl)phosphateincreases expression1
sodium arseniteincreases expression1
butyraldehydeincreases expression1
licochalcone Bincreases expression1
PCI 5002increases expression, affects cotreatment1
Acetaminophenincreases expression1
Air Pollutantsincreases abundance, increases expression1
Copperaffects binding, decreases expression1
Disulfiramaffects binding, decreases expression1
Hydrogen Peroxideaffects expression1
Mustard Gasincreases expression1
Silverincreases expression1
Sodium Dodecyl Sulfateincreases expression1
Thiramincreases expression1
Valproic Acidincreases expression1
Zincaffects cotreatment, increases expression1
Copper Sulfateincreases expression1
Acrylamideincreases expression1
Particulate Matterincreases abundance, increases expression1

Cellosaurus cell lines

2 cell lines: 2 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_2106M-07eCancer cell lineFemale
CVCL_RM07M-07e/TPOCancer cell lineFemale

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.