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Items: 1 to 50 of 52

1.

Characterisation of tumour microenvironment and immune checkpoints in primary central nervous system diffuse large B cell lymphomas.

Alame M, Pirel M, Costes-Martineau V, Bauchet L, Fabbro M, Tourneret A, De Oliveira L, Durand L, Roger P, Gonzalez S, Cacheux V, Rigau V, Szablewski V.

Virchows Arch. 2019 Dec 6. doi: 10.1007/s00428-019-02695-6. [Epub ahead of print]

PMID:
31811434
2.

Human herpesvirus 6 infection after autologous stem cell transplantation: A multicenter prospective study in adult patients.

Balsat M, Pillet S, Tavernier E, Cacheux V, Escuret V, Moluçon-Chabrot C, Augeul-Meunier K, Mirand A, Regagnon C, Tinquaut F, Bousser V, Oriol M, Guyotat D, Salles G, Bay JO, Pozzetto B, Cornillon J.

J Infect. 2019 Jul;79(1):36-42. doi: 10.1016/j.jinf.2019.05.001. Epub 2019 May 7.

PMID:
31075291
3.

Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene.

Auboyer L, Monzo C, Wallon D, Rovelet-Lecrux A, Gabelle A, Gazagne I, Cacheux V, Lehmann S, Crozet C.

Stem Cell Res. 2019 May;37:101438. doi: 10.1016/j.scr.2019.101438. Epub 2019 Apr 15.

4.

Systemic, primary cutaneous, and breast implant-associated ALK-negative anaplastic large-cell lymphomas present similar biologic features despite distinct clinical behavior.

Gerbe A, Alame M, Dereure O, Gonzalez S, Durand L, Tempier A, De Oliveira L, Tourneret A, Costes-Martineau V, Cacheux V, Szablewski V.

Virchows Arch. 2019 Aug;475(2):163-174. doi: 10.1007/s00428-019-02570-4. Epub 2019 Apr 6.

PMID:
30953147
5.

Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene.

Auboyer L, Monzo C, Wallon D, Rovelet-Lecrux A, Gabelle A, Gazagne I, Cacheux V, Lehmann S, Crozet C.

Stem Cell Res. 2019 Jan;34:101381. doi: 10.1016/j.scr.2018.101381. Epub 2019 Jan 3.

6.

Cutaneous localization of angioimmunoblastic T-cell lymphoma may masquerade as B-cell lymphoma or classical Hodgkin lymphoma: A histologic diagnostic pitfall.

Szablewski V, Dereure O, René C, Tempier A, Durand L, Alame M, Cacheux V, Costes-Martineau V.

J Cutan Pathol. 2019 Feb;46(2):102-110. doi: 10.1111/cup.13382. Epub 2018 Dec 10.

PMID:
30370547
7.

Cutaneous presentation preceding acute myeloid leukemia with CD4+/CD56+ expression misdiagnosed as a blastic plasmocytoid dendritic cell neoplasm: A case report.

Szablewski V, Costes V, Bret C, Dereure O, Yosr H, Alame M, Cacheux V.

J Cutan Pathol. 2018 Aug;45(8):610-614. doi: 10.1111/cup.13257. Epub 2018 May 22.

PMID:
29660158
8.

Diagnostic value of STMN1, LMO2, HGAL, AID expression and 1p36 chromosomal abnormalities in primary cutaneous B cell lymphomas.

Verdanet E, Dereure O, René C, Tempier A, Benammar-Hafidi A, Gallo M, Frouin E, Durand L, Gazagne I, Costes-Martineau V, Cacheux V, Szablewski V.

Histopathology. 2017 Oct;71(4):648-660. doi: 10.1111/his.13279. Epub 2017 Jul 19.

PMID:
28594133
9.

Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in neurodevelopmental disorders.

Aksoy I, Utami KH, Winata CL, Hillmer AM, Rouam SL, Briault S, Davila S, Stanton LW, Cacheux V.

Hum Mol Genet. 2017 Jan 15;26(2):367-382. doi: 10.1093/hmg/ddw393.

PMID:
28365779
10.

Development of a continuous process for α-thio-β-chloroacrylamide synthesis with enhanced control of a cascade transformation.

Dennehy OC, Cacheux VM, Deadman BJ, Lynch D, Collins SG, Moynihan HA, Maguire AR.

Beilstein J Org Chem. 2016 Nov 24;12:2511-2522. doi: 10.3762/bjoc.12.246. eCollection 2016.

11.

PD1 and PDL1 expression in primary central nervous system diffuse large B-cell lymphoma are frequent and expression of PD1 predicts poor survival.

Four M, Cacheux V, Tempier A, Platero D, Fabbro M, Marin G, Leventoux N, Rigau V, Costes-Martineau V, Szablewski V.

Hematol Oncol. 2017 Dec;35(4):487-496. doi: 10.1002/hon.2375. Epub 2016 Dec 13.

PMID:
27966264
12.

Leukemic non-nodal mantle cell lymphomas have a distinct phenotype and are associated with deletion of PARP1 and 13q14.

Gallo M, Cacheux V, Vincent L, Bret C, Tempier A, Guittard C, Macé A, Leventoux N, Costes V, Szablewski V.

Virchows Arch. 2016 Dec;469(6):697-706. Epub 2016 Sep 7.

PMID:
27605053
13.

Acute lymphoblastic leukemia in the context of RASopathies.

Cavé H, Caye A, Strullu M, Aladjidi N, Vignal C, Ferster A, Méchinaud F, Domenech C, Pierri F, Contet A, Cacheux V, Irving J, Kratz C, Clavel J, Verloes A.

Eur J Med Genet. 2016 Mar;59(3):173-8. doi: 10.1016/j.ejmg.2016.01.003. Epub 2016 Feb 5.

PMID:
26855057
14.

Cerebral venous thrombosis in adult patients with acute lymphoblastic leukemia or lymphoblastic lymphoma during induction chemotherapy with l-asparaginase: The GRAALL experience.

Couturier MA, Huguet F, Chevallier P, Suarez F, Thomas X, Escoffre-Barbe M, Cacheux V, Pignon JM, Bonmati C, Sanhes L, Bories P, Daguindau E, Dorvaux V, Reman O, Frayfer J, Orvain C, Lhéritier V, Ifrah N, Dombret H, Hunault-Berger M, Tanguy-Schmidt A.

Am J Hematol. 2015 Nov;90(11):986-91. doi: 10.1002/ajh.24130. Epub 2015 Oct 8.

15.

Impaired development of neural-crest cell-derived organs and intellectual disability caused by MED13L haploinsufficiency.

Utami KH, Winata CL, Hillmer AM, Aksoy I, Long HT, Liany H, Chew EG, Mathavan S, Tay SK, Korzh V, Sarda P, Davila S, Cacheux V.

Hum Mutat. 2014 Nov;35(11):1311-20. doi: 10.1002/humu.22636. Epub 2014 Sep 23. Review.

PMID:
25137640
16.

Detection of chromosomal breakpoints in patients with developmental delay and speech disorders.

Utami KH, Hillmer AM, Aksoy I, Chew EG, Teo AS, Zhang Z, Lee CW, Chen PJ, Seng CC, Ariyaratne PN, Rouam SL, Soo LS, Yousoof S, Prokudin I, Peters G, Collins F, Wilson M, Kakakios A, Haddad G, Menuet A, Perche O, Tay SK, Sung KW, Ruan X, Ruan Y, Liu ET, Briault S, Jamieson RV, Davila S, Cacheux V.

PLoS One. 2014 Mar 6;9(6):e90852. doi: 10.1371/journal.pone.0090852. eCollection 2014.

17.

Autologous stem cell transplantation in mantle cell lymphoma: a report from the SFGM-TC.

Touzeau C, Leux C, Bouabdallah R, Roussel M, Delarue R, Bouabdallah K, Thieblemont C, Cacheux V, Cartron G, Compain L, Gyan E, Morschhauser F, Casasnovas O, Moles MP, Michallet AS, Gressin R, Damaj G, Rose C, Sirvent A, Hermine O, Mohty M, Milpied N, Le Gouill S.

Ann Hematol. 2014 Feb;93(2):233-42. doi: 10.1007/s00277-013-1860-8.

PMID:
24563925
18.

Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.

Perche O, Menuet A, Marcos M, Liu L, Pâris A, Utami KH, Kervran D, Cacheux V, Laudier B, Briault S.

Eur J Med Genet. 2013 Nov;56(11):635-41. doi: 10.1016/j.ejmg.2013.07.007. Epub 2013 Sep 4.

PMID:
24013099
19.

[Ruxolitinib prescription in myelofibrosis].

Lemal R, Robin M, Ravinet A, Cacheux V, Guièze R, Bay JO.

Bull Cancer. 2013 Sep;100(9):897-902. doi: 10.1684/bdc.2013.1792. Review. French.

PMID:
23985569
20.

Autologous stem cell transplantation in mantle cell lymphoma: a report from the SFGM-TC.

Touzeau C, Leux C, Bouabdallah R, Roussel M, Delarue R, Bouabdallah K, Thieblemont C, Cacheux V, Cartron G, Compain L, Gyan E, Morschhauser F, Casasnovas O, Moles MP, Michallet AS, Gressin R, Damaj G, Rose C, Sirvent A, Hermine O, Mohty M, Milpied N, Le Gouill S.

Ann Hematol. 2014 Feb;93(2):233-42. doi: 10.1007/s00277-013-1860-8. Epub 2013 Aug 16.

PMID:
23949376
21.

CD44-SLC1A2 gene fusions in gastric cancer.

Tao J, Deng NT, Ramnarayanan K, Huang B, Oh HK, Leong SH, Lim SS, Tan IB, Ooi CH, Wu J, Lee M, Zhang S, Rha SY, Chung HC, Smoot DT, Ashktorab H, Kon OL, Cacheux V, Yap C, Palanisamy N, Tan P.

Sci Transl Med. 2011 Apr 6;3(77):77ra30. doi: 10.1126/scitranslmed.3001423.

22.

Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosis.

Lissandre S, Bay JO, Cahn JY, Porcher R, Cacheux V, Cabrespine A, Cornillon J, Cassinat B, Peffault de Latour R, Socie G, Robin M.

Bone Marrow Transplant. 2011 Apr;46(4):557-61. doi: 10.1038/bmt.2010.276. Epub 2010 Nov 1.

PMID:
21042309
23.

Allogeneic hematopoietic stem cell transplantation allows long-term complete remission and curability in high-risk Waldenström’s macroglobulinemia. Results of a retrospective analysis of the Société Française de Greffe de Moelle et de Thérapie Cellulaire.

Garnier A, Robin M, Larosa F, Golmard JL, Le Gouill S, Coiteux V, Tabrizi R, Bulabois CE, Cacheux V, Kuentz M, Dreyfus B, Dreger P, Rio B, Moles-Moreau MP, Bilger K, Bay JO, Leblond V, Blaise D, Tournilhac O, Dhédin N.

Haematologica. 2010 Jun;95(6):950-5. doi: 10.3324/haematol.2009.017814. Epub 2010 Jan 15.

24.

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.

Bruno DL, Ganesamoorthy D, Schoumans J, Bankier A, Coman D, Delatycki M, Gardner RJ, Hunter M, James PA, Kannu P, McGillivray G, Pachter N, Peters H, Rieubland C, Savarirayan R, Scheffer IE, Sheffield L, Tan T, White SM, Yeung A, Bowman Z, Ngo C, Choy KW, Cacheux V, Wong L, Amor DJ, Slater HR.

J Med Genet. 2009 Feb;46(2):123-31. doi: 10.1136/jmg.2008.062604. Epub 2008 Nov 17.

PMID:
19015223
25.

Cytogenetic studies of 24 renal epithelial tumors with von Hippel-Lindau and fragile histidine triad protein expression correlation.

Gayrard N, Cacheux V, Iborra F, Mourad G, Argilés A.

Arch Pathol Lab Med. 2008 Jun;132(6):965-73. doi: 10.1043/1543-2165(2008)132[965:CSORET]2.0.CO;2.

PMID:
18517280
26.

Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the "Mowat-Wilson" syndrome.

Bassez G, Camand OJ, Cacheux V, Kobetz A, Dastot-Le Moal F, Marchant D, Catala M, Abitbol M, Goossens M.

Neurobiol Dis. 2004 Mar;15(2):240-50.

PMID:
15006694
27.

Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B.

Wilson M, Mowat D, Dastot-Le Moal F, Cacheux V, Kääriäinen H, Cass D, Donnai D, Clayton-Smith J, Townshend S, Curry C, Gattas M, Braddock S, Kerr B, Aftimos S, Zehnwirth H, Barrey C, Goossens M.

Am J Med Genet A. 2003 Jun 15;119A(3):257-65.

PMID:
12784289
28.

Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella.

Pennarun G, Bridoux AM, Escudier E, Dastot-Le Moal F, Cacheux V, Amselem S, Duriez B.

Am J Respir Cell Mol Biol. 2002 Mar;26(3):362-70.

PMID:
11867345
29.

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease.

Cacheux V, Dastot-Le Moal F, Kääriäinen H, Bondurand N, Rintala R, Boissier B, Wilson M, Mowat D, Goossens M.

Hum Mol Genet. 2001 Jul 1;10(14):1503-10.

PMID:
11448942
30.

The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia.

Pennarun G, Chapelin C, Escudier E, Bridoux AM, Dastot F, Cacheux V, Goossens M, Amselem S, Duriez B.

Hum Genet. 2000 Dec;107(6):642-9.

PMID:
11153919
31.

Polydom: a secreted protein with pentraxin, complement control protein, epidermal growth factor and von Willebrand factor A domains.

Gilgès D, Vinit MA, Callebaut I, Coulombel L, Cacheux V, Romeo PH, Vigon I.

Biochem J. 2000 Nov 15;352 Pt 1:49-59.

32.

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.

Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, Marcos E, Duriez B, Cacheux V, Moers Av, Goossens M, Grüters A, Amselem S.

Nat Genet. 2000 Jun;25(2):182-6.

PMID:
10835633
33.

Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.

Lapierre JM, Cacheux V, Luton D, Collot N, Oury JF, Aurias A, Tachdjian G.

Prenat Diagn. 2000 Feb;20(2):123-31.

PMID:
10694684
34.

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

Pennarun G, Escudier E, Chapelin C, Bridoux AM, Cacheux V, Roger G, Clément A, Goossens M, Amselem S, Duriez B.

Am J Hum Genet. 1999 Dec;65(6):1508-19.

35.

De novo inverted duplication 9p21pter involving telomeric repeated sequences.

Sanlaville D, Baumann C, Lapierre JM, Romana S, Collot N, Cacheux V, Turleau C, Tachdjian G.

Am J Med Genet. 1999 Mar 12;83(2):125-31. Review.

PMID:
10190483
36.

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G.

Ann Genet. 1998;41(3):133-40.

PMID:
9833066
37.

Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency.

Duquesnoy P, Roy A, Dastot F, Ghali I, Teinturier C, Netchine I, Cacheux V, Hafez M, Salah N, Chaussain JL, Goossens M, Bougnères P, Amselem S.

FEBS Lett. 1998 Oct 23;437(3):216-20.

38.

Pentasomy 13q in a case of acute myelogenous leukemia (Mo).

Ramond S, Cacheux V, Ciaudo M, Cadiou M, Perrot JY, Delmer A, Viguié F, Zittoun R, Marie JP.

Cancer Genet Cytogenet. 1998 Nov;107(1):73-5.

PMID:
9809039
39.

Altered patterns of DNA methylation on chromosomes from leukemia cell lines: identification of 5-methylcytosines by indirect immunodetection.

Bensaada M, Kiefer H, Tachdjian G, Lapierre JM, Cacheux V, Niveleau A, Métézeau P.

Cancer Genet Cytogenet. 1998 Jun;103(2):101-9.

PMID:
9614907
40.

Comparative genomic hybridization: technical development and cytogenetic aspects for routine use in clinical laboratories.

Lapierre JM, Cacheux V, Da Silva F, Collot N, Hervy N, Wiss J, Tachdjian G.

Ann Genet. 1998;41(1):56-62. Erratum in: Ann Genet 1998;41(2):87.

PMID:
9599653
41.

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia.

Cavé H, Cacheux V, Raynaud S, Brunie G, Bakkus M, Cochaux P, Preudhomme C, Laï JL, Vilmer E, Grandchamp B.

Leukemia. 1997 Sep;11(9):1459-64.

42.

Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children.

Gérard B, Le Heuzey MF, Brunie G, Lewine P, Saiag MC, Cacheux V, Da Silva F, Dugas M, Mouren-Simeoni MC, Elion J, Grandchamp B.

Ann Genet. 1997;40(3):139-44.

PMID:
9401101
43.

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia.

Raynaud S, Cave H, Baens M, Bastard C, Cacheux V, Grosgeorge J, Guidal-Giroux C, Guo C, Vilmer E, Marynen P, Grandchamp B.

Blood. 1996 Apr 1;87(7):2891-9.

PMID:
8639909
44.

Expression of p13MTCP1 is restricted to mature T-cell proliferations with t(X;14) translocations.

Madani A, Choukroun V, Soulier J, Cacheux V, Claisse JF, Valensi F, Daliphard S, Cazin B, Levy V, Leblond V, Daniel MT, Sigaux F, Stern MH.

Blood. 1996 Mar 1;87(5):1923-7.

PMID:
8634440
45.

[Waardenburg's syndrome].

Cacheux V, Delezoide AL, Vekemans M.

C R Seances Soc Biol Fil. 1996;190(5-6):577-80. French.

PMID:
9074723
46.

[New techniques in cytogenetics].

Tachdjian G, Cacheux V, Romana S.

Arch Pediatr. 1996;3 Suppl 1:351s-352s. French. No abstract available.

PMID:
8796077
47.

Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3.

Martin E, Cacheux V, Cavé H, Lapierre JM, Le Paslier D, Grandchamp B.

Hum Genet. 1995 Dec;96(6):668-70.

PMID:
8522324
48.

Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometry.

Tachdjian G, Cacheux V, Kiefer H, Druart L, Lapierre JM, Oury JF, Blot P, Metezeau P.

Fetal Diagn Ther. 1995 Nov-Dec;10(6):387-92.

PMID:
8579777
49.

The MTCP-1/c6.1B gene encodes for a cytoplasmic 8 kD protein overexpressed in T cell leukemia bearing a t(X;14) translocation.

Soulier J, Madani A, Cacheux V, Rosenzwajg M, Sigaux F, Stern MH.

Oncogene. 1994 Dec;9(12):3565-70.

PMID:
7970717
50.

Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12.

Cacheux V, Martasek P, Fougerousse F, Delfau MH, Druart L, Tachdjian G, Grandchamp B.

Hum Genet. 1994 Nov;94(5):557-9.

PMID:
7959694

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