Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 165

1.

The TGFB2-AS1 lncRNA Regulates TGF-β Signaling by Modulating Corepressor Activity.

Papoutsoglou P, Tsubakihara Y, Caja L, Morén A, Pallis P, Ameur A, Heldin CH, Moustakas A.

Cell Rep. 2019 Sep 17;28(12):3182-3198.e11. doi: 10.1016/j.celrep.2019.08.028.

PMID:
31533040
2.

Goodbye reference, hello genome graphs.

Ameur A.

Nat Biotechnol. 2019 Aug;37(8):866-868. doi: 10.1038/s41587-019-0199-7. No abstract available.

PMID:
31375808
3.

Pelvic salvage (SBRT) radiotherapy based on 68Ga-PSMA PET/CT: About a case.

Slaoui A, Desmet A, Regragui S, Mesfioui A, Ameur A, Peltier A.

Urol Case Rep. 2019 Jan 17;23:95-96. doi: 10.1016/j.eucr.2019.01.014. eCollection 2019 Mar.

4.

A systematic review of contemporary management of oligometastatic prostate cancer: fighting a challenge or tilting at windmills?

Slaoui A, Albisinni S, Aoun F, Assenmacher G, Al Hajj Obeid W, Diamand R, Regragui S, Touzani A, Bakar A, Mesfioui A, Karmouni T, Ameur A, Elkhader K, Koutani A, Ibnattya A, Roumeguere T, Peltier A.

World J Urol. 2019 Jan 31. doi: 10.1007/s00345-019-02652-7. [Epub ahead of print]

PMID:
30706122
5.

The Versatility of SMRT Sequencing.

Hestand MS, Ameur A.

Genes (Basel). 2019 Jan 4;10(1). pii: E24. doi: 10.3390/genes10010024.

6.

Invasive cervical tumors with high and low HPV titer represent molecular subgroups with different disease etiology.

Cui T, Enroth S, Ameur A, Gustavsson I, Lindquist D, Gyllensten U.

Carcinogenesis. 2019 Apr 29;40(2):269-278. doi: 10.1093/carcin/bgy183.

PMID:
30596972
7.

Grounding evidence in experience to support people-centered health services.

Dion A, Joseph L, Jimenez V, Gutierrez AC, Ben Ameur A, Robert E, Andersson N.

Int J Public Health. 2019 Jun;64(5):797-802. doi: 10.1007/s00038-018-1180-9. Epub 2018 Dec 12. No abstract available.

8.

Expression profiling and in situ screening of circular RNAs in human tissues.

Zaghlool A, Ameur A, Wu C, Westholm JO, Niazi A, Manivannan M, Bramlett K, Nilsson M, Feuk L.

Sci Rep. 2018 Nov 16;8(1):16953. doi: 10.1038/s41598-018-35001-6.

9.

De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data.

Ameur A, Che H, Martin M, Bunikis I, Dahlberg J, Höijer I, Häggqvist S, Vezzi F, Nordlund J, Olason P, Feuk L, Gyllensten U.

Genes (Basel). 2018 Oct 9;9(10). pii: E486. doi: 10.3390/genes9100486.

10.

Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype.

Frykholm C, Klar J, Tomanovic T, Ameur A, Dahl N.

Eur J Hum Genet. 2018 Dec;26(12):1871-1874. doi: 10.1038/s41431-018-0256-6. Epub 2018 Sep 24.

PMID:
30250054
11.

Single-Molecule Sequencing: Towards Clinical Applications.

Ameur A, Kloosterman WP, Hestand MS.

Trends Biotechnol. 2019 Jan;37(1):72-85. doi: 10.1016/j.tibtech.2018.07.013. Epub 2018 Aug 13. Review.

PMID:
30115375
12.

Evaluation of glutathione S-transferase pi 1 expression and gene promoter methylation in Moroccan patients with urothelial bladder cancer.

Hadami K, Dakka N, Bensaid M, El Ahanidi H, Ameur A, Chahdi H, Oukabli M, Al Bouzidi A, Attaleb M, El Mzibri M.

Mol Genet Genomic Med. 2018 Sep;6(5):819-827. doi: 10.1002/mgg3.449. Epub 2018 Jul 24.

13.

[Traumatic dissection of the left renal pedicle in a young adult].

Zoulati M, Slaoui A, Bakkali T, Aghoutane N, Lyazidi Y, Chtata H, Janane A, Ameur A, Taberkant M.

J Med Vasc. 2018 Jul;43(4):272-276. doi: 10.1016/j.jdmv.2018.05.004. Epub 2018 May 30. French.

PMID:
29981737
14.

Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing.

Höijer I, Tsai YC, Clark TA, Kotturi P, Dahl N, Stattin EL, Bondeson ML, Feuk L, Gyllensten U, Ameur A.

Hum Mutat. 2018 Sep;39(9):1262-1272. doi: 10.1002/humu.23580. Epub 2018 Jul 12.

15.

A novel ECEL1 mutation expands the phenotype of distal arthrogryposis multiplex congenita type 5D to include pretibial vertical skin creases.

Stattin EL, Johansson J, Gudmundsson S, Ameur A, Lundberg S, Bondeson ML, Wilbe M.

Am J Med Genet A. 2018 Jun;176(6):1405-1410. doi: 10.1002/ajmg.a.38691. Epub 2018 Apr 16.

PMID:
29663639
16.

Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics.

Ardui S, Ameur A, Vermeesch JR, Hestand MS.

Nucleic Acids Res. 2018 Mar 16;46(5):2159-2168. doi: 10.1093/nar/gky066. Review.

17.

[Prognostic of older age for patients with invasive-muscle-bladder cancer and treated by radical cystectomy].

Dehayni Y, Tetou M, Khdach Y, Janane A, Alami M, Ameur A.

Prog Urol. 2018 Mar;28(3):166-172. doi: 10.1016/j.purol.2017.12.005. Epub 2018 Jan 9. French.

PMID:
29329898
18.

Single-molecule DNA sequencing of acute myeloid leukemia and myelodysplastic syndromes with multiple TP53 alterations.

Lodé L, Ameur A, Coste T, Ménard A, Richebourg S, Gaillard JB, Le Bris Y, Béné MC, Lavabre-Bertrand T, Soussi T.

Haematologica. 2018 Jan;103(1):e13-e16. doi: 10.3324/haematol.2017.176719. Epub 2017 Oct 27. No abstract available.

19.

A novel approach using long-read sequencing and ddPCR to investigate gonadal mosaicism and estimate recurrence risk in two families with developmental disorders.

Wilbe M, Gudmundsson S, Johansson J, Ameur A, Stattin EL, Annerén G, Malmgren H, Frykholm C, Bondeson ML.

Prenat Diagn. 2017 Nov;37(11):1146-1154. doi: 10.1002/pd.5156. Epub 2017 Oct 17.

20.

[Bellini duct carcinoma: a new case study and literature review].

El Bahri A, Chafiki J, Louardi N, Jendouzi O, Janane A, Ameur A, Abbar M.

Pan Afr Med J. 2017 Jul 4;27:166. doi: 10.11604/pamj.2017.27.166.9271. eCollection 2017. Review. French.

21.

SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.

Ameur A, Dahlberg J, Olason P, Vezzi F, Karlsson R, Martin M, Viklund J, Kähäri AK, Lundin P, Che H, Thutkawkorapin J, Eisfeldt J, Lampa S, Dahlberg M, Hagberg J, Jareborg N, Liljedahl U, Jonasson I, Johansson Å, Feuk L, Lundeberg J, Syvänen AC, Lundin S, Nilsson D, Nystedt B, Magnusson PK, Gyllensten U.

Eur J Hum Genet. 2017 Nov;25(11):1253-1260. doi: 10.1038/ejhg.2017.130. Epub 2017 Aug 23.

22.

Identification of G2607A mutation in EGFR gene with a significative rate in Moroccan patients with Bladder Cancer.

El Hamdani W, Hadami K, Bensaid M, El Ahanidi H, Ameur A, Filali Maltouf A, Abbar M, Attaleb M, Albouzidi A, El Mzibri M.

Cell Mol Biol (Noisy-le-grand). 2017 May 20;63(5):75-81. doi: 10.14715/cmb/2017.63.5.14.

PMID:
28719349
23.

Large prostatic stones with staghorn renal calculus in a 61-year-old man: an unusual presentation of uncommon disease.

Hajji F, Lmezguidi K, Janane A, Ameur A.

BMJ Case Rep. 2017 Jun 29;2017. pii: bcr-2017-219778. doi: 10.1136/bcr-2017-219778.

24.

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

Stattin EL, Henning P, Klar J, McDermott E, Stecksen-Blicks C, Sandström PE, Kellgren TG, Rydén P, Hallmans G, Lönnerholm T, Ameur A, Helfrich MH, Coxon FP, Dahl N, Wikström J, Lerner UH.

Sci Rep. 2017 Jun 7;7(1):3012. doi: 10.1038/s41598-017-02533-2.

25.

Expression of human epidermal growth factor receptor 2 in bladder urothelial carcinoma.

El Ochi MR, Oukabli M, Bouaiti E, Chahdi H, Boudhas A, Allaoui M, Ameur A, Abbar M, Al Bouzidi A.

BMC Clin Pathol. 2017 Apr 4;17:3. doi: 10.1186/s12907-017-0046-z. eCollection 2017.

26.

A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy.

Bondeson ML, Ericson K, Gudmundsson S, Ameur A, Pontén F, Wesström J, Frykholm C, Wilbe M.

Clin Genet. 2017 Nov;92(5):510-516. doi: 10.1111/cge.13012. Epub 2017 May 3.

PMID:
28295209
27.

Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26.

Gudmundsson S, Wilbe M, Ekvall S, Ameur A, Cahill N, Alexandrov LB, Virtanen M, Hellström Pigg M, Vahlquist A, Törmä H, Bondeson ML.

Hum Mol Genet. 2017 Mar 15;26(6):1070-1077. doi: 10.1093/hmg/ddx017.

28.

Association between GPX1 Pro189Leu polymorphism and the occurrence of bladder cancer in Morocco.

Hadami K, Ameziane El Hassani R, Ameur A, Dakka N, Abbar M, Al Bouzidi A, Attaleb M, El Mzibri M.

Cell Mol Biol (Noisy-le-grand). 2016 Dec 30;62(14):38-43. doi: 10.14715/cmb/ 2016.62.14.6.

PMID:
28145855
29.

PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c.

Pan G, Ameur A, Enroth S, Bysani M, Nord H, Cavalli M, Essand M, Gyllensten U, Wadelius C.

Nucleic Acids Res. 2017 Mar 17;45(5):2408-2422. doi: 10.1093/nar/gkw1186.

30.

Pathological outcomes and agressiveness of low-risk prostate cancer in Northern African men.

Ammani A, Janane A, Bouzide B, Dehayni Y, Lezrek M, Ghadouane M, Ameur A, Abbar M, Qarro A, Alami M.

Actas Urol Esp. 2016 Nov;40(9):556-563. doi: 10.1016/j.acuro.2016.01.011. Epub 2016 May 6. English, Spanish.

PMID:
27161090
31.

A novel variant in MYLK causes thoracic aortic dissections: genotypic and phenotypic description.

Hannuksela M, Stattin EL, Klar J, Ameur A, Johansson B, Sörensen K, Carlberg B.

BMC Med Genet. 2016 Sep 1;17(1):61. doi: 10.1186/s12881-016-0326-y.

32.

Large Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland Ponies.

Rafati N, Andersson LS, Mikko S, Feng C, Raudsepp T, Pettersson J, Janecka J, Wattle O, Ameur A, Thyreen G, Eberth J, Huddleston J, Malig M, Bailey E, Eichler EE, Dalin G, Chowdary B, Andersson L, Lindgren G, Rubin CJ.

G3 (Bethesda). 2016 Jul 7;6(7):2213-23. doi: 10.1534/g3.116.029645.

33.

Identification of novel genetic causes of Rett syndrome-like phenotypes.

Lopes F, Barbosa M, Ameur A, Soares G, de Sá J, Dias AI, Oliveira G, Cabral P, Temudo T, Calado E, Cruz IF, Vieira JP, Oliveira R, Esteves S, Sauer S, Jonasson I, Syvänen AC, Gyllensten U, Pinto D, Maciel P.

J Med Genet. 2016 Mar;53(3):190-9. doi: 10.1136/jmedgenet-2015-103568. Epub 2016 Jan 6.

PMID:
26740508
34.

Analysis of hepatitis C NS5A resistance associated polymorphisms using ultra deep single molecule real time (SMRT) sequencing.

Bergfors A, Leenheer D, Bergqvist A, Ameur A, Lennerstrand J.

Antiviral Res. 2016 Feb;126:81-9. doi: 10.1016/j.antiviral.2015.12.005. Epub 2015 Dec 19.

PMID:
26707078
35.

[Flexible laser ureteroscopy in the treatment of upper urinary tract stones: results about 166 interventions].

Padja E, Ibarra VA, Lmezguidi K, Janane A, Ghadouane M, Ameur A, Abbar M.

Pan Afr Med J. 2015 Sep 8;22:13. doi: 10.11604/pamj.2015.22.13.7591. eCollection 2015. French. No abstract available.

36.

Upper urinary tract lipoma: A case report.

Lmezguidi K, Hajji F, Sinaa M, Janane A, Ghadouane M, Ameur A, Albouzidi A, Abbar M.

Can Urol Assoc J. 2015 Sep-Oct;9(9-10):E673-5. doi: 10.5489/cuaj.2555. Epub 2015 Sep 9.

37.

Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.

Einarsdottir E, Svensson I, Darki F, Peyrard-Janvid M, Lindvall JM, Ameur A, Jacobsson C, Klingberg T, Kere J, Matsson H.

Hum Genet. 2015 Nov;134(11-12):1239-48. doi: 10.1007/s00439-015-1602-1. Epub 2015 Sep 23.

38.

Determination of obesity associated gene variants related to TMEM18 through ultra-deep targeted re-sequencing in a case-control cohort for pediatric obesity.

Rask-Andersen M, Sällman Almén M, Jacobsson JA, Ameur A, Moschonis G, Dedoussis G, Marcus C, Gyllensten U, Fredriksson R, Schiöth HB.

Genet Res (Camb). 2015 Sep 14;97:e16. doi: 10.1017/S0016672315000117.

PMID:
26365393
39.

Transcriptome Profiling Reveals Degree of Variability in Induced Pluripotent Stem Cell Lines: Impact for Human Disease Modeling.

Schuster J, Halvardson J, Pilar Lorenzo L, Ameur A, Sobol M, Raykova D, Annerén G, Feuk L, Dahl N.

Cell Reprogram. 2015 Oct;17(5):327-37. doi: 10.1089/cell.2015.0009. Epub 2015 Sep 8.

PMID:
26348590
40.

Role of the AMP kinase in cytokine-induced human EndoC-βH1 cell death.

Fred RG, Kappe C, Ameur A, Cen J, Bergsten P, Ravassard P, Scharfmann R, Welsh N.

Mol Cell Endocrinol. 2015 Oct 15;414:53-63. doi: 10.1016/j.mce.2015.07.015. Epub 2015 Jul 26.

PMID:
26213325
41.

Gossypiboma.

Hajji F, Ameur A.

Pan Afr Med J. 2015 Apr 7;20:332. doi: 10.11604/pamj.2015.20.332.6609. eCollection 2015. No abstract available.

42.

Emphysematous cystitis with concomitant bilateral emphysematous ureteritis and pyelitis in a diabetic patient.

Hajji F, Ameur A.

Pan Afr Med J. 2015 Apr 6;20:324. doi: 10.11604/pamj.2015.20.324.6657. eCollection 2015. No abstract available.

43.

Butterfly hematoma after traumatic intercourse.

Hajji F, Ameur A.

Pan Afr Med J. 2015 Apr 1;20:317. doi: 10.11604/pamj.2015.20.317.6660. eCollection 2015. No abstract available.

44.

Differential Expression Analysis by RNA-Seq Reveals Perturbations in the Platelet mRNA Transcriptome Triggered by Pathogen Reduction Systems.

Osman A, Hitzler WE, Ameur A, Provost P.

PLoS One. 2015 Jul 14;10(7):e0133070. doi: 10.1371/journal.pone.0133070. eCollection 2015.

45.

Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing.

Cavelier L, Ameur A, Häggqvist S, Höijer I, Cahill N, Olsson-Strömberg U, Hermanson M.

BMC Cancer. 2015 Feb 12;15:45. doi: 10.1186/s12885-015-1046-y.

46.

Phenotypic expansion of visceral myopathy associated with ACTG2 tandem base substitution.

Klar J, Raykova D, Gustafson E, Tóthová I, Ameur A, Wanders A, Dahl N.

Eur J Hum Genet. 2015 Dec;23(12):1679-83. doi: 10.1038/ejhg.2015.49. Epub 2015 Mar 18.

47.

Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer.

Mengelbier LH, Karlsson J, Lindgren D, Valind A, Lilljebjörn H, Jansson C, Bexell D, Braekeveldt N, Ameur A, Jonson T, Kultima HG, Isaksson A, Asmundsson J, Versteeg R, Rissler M, Fioretos T, Sandstedt B, Börjesson A, Backman T, Pal N, Øra I, Mayrhofer M, Gisselsson D.

Nat Commun. 2015 Jan 27;6:6125. doi: 10.1038/ncomms7125.

PMID:
25625758
48.

MuSK: a new target for lethal fetal akinesia deformation sequence (FADS).

Wilbe M, Ekvall S, Eurenius K, Ericson K, Casar-Borota O, Klar J, Dahl N, Ameur A, Annerén G, Bondeson ML.

J Med Genet. 2015 Mar;52(3):195-202. doi: 10.1136/jmedgenet-2014-102730. Epub 2015 Jan 22.

PMID:
25612909
49.

[Acute pyelonephritis in pregnant women: place of medical treatment and indications for drainage of the upper urinary tract (Are there predictive clinical, biological and radiological factors to make the drainage acceptable?)].

El Bahri A, Janane A, Chafiki J, Arnaud T, Ghadouane M, Ameur A, Abbar M.

Pan Afr Med J. 2015 Dec 2;22:324. doi: 10.11604/pamj.2015.22.324.7262. eCollection 2015. French. No abstract available.

50.

Torsion of the appendix testis in an undescended testicle.

Hajji F, Ameur A.

Pan Afr Med J. 2015 Nov 20;22:265. doi: 10.11604/pamj.2015.22.265.7493. eCollection 2015. No abstract available.

Supplemental Content

Support Center