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Items: 1 to 50 of 114

1.

Microfluidic Assembly of siRNA-Loaded Micelleplexes for Tumor Targeting in an Orthotopic Model of Ovarian Cancer.

Feldmann DP, Jones S, Douglas K, Shields AF, Merkel OM.

Methods Mol Biol. 2019;1974:355-369. doi: 10.1007/978-1-4939-9220-1_24.

PMID:
31099014
2.

Baboon (Papio ursinus) single fibre contractile properties are similar to that of trained humans.

Dada S, Henning F, Feldmann DC, Kohn TA.

J Muscle Res Cell Motil. 2018 Dec;39(5-6):189-199. doi: 10.1007/s10974-019-09509-x. Epub 2019 Mar 20.

PMID:
30895442
3.

Evaluating the Regulation of Cytokine Levels After siRNA Treatment in Antigen-Specific Target Cell Populations via Intracellular Staining.

Kandil R, Feldmann D, Xie Y, Merkel OM.

Methods Mol Biol. 2019;1943:323-331. doi: 10.1007/978-1-4939-9092-4_21.

PMID:
30838626
4.

In vitro and in vivo delivery of siRNA via VIPER polymer system to lung cells.

Feldmann DP, Cheng Y, Kandil R, Xie Y, Mohammadi M, Harz H, Sharma A, Peeler DJ, Moszczynska A, Leonhardt H, Pun SH, Merkel OM.

J Control Release. 2018 Apr 28;276:50-58. doi: 10.1016/j.jconrel.2018.02.017. Epub 2018 Feb 20.

5.

PARP-1/PAR Activity in Cultured Human Lens Epithelial Cells Exposed to Two Levels of UVB Light.

Cencer CS, Chintala SK, Townsend TJ, Feldmann DP, Awrow MA, Putris NA, Geno ME, Donovan MG, Giblin FJ.

Photochem Photobiol. 2018 Jan;94(1):126-138. doi: 10.1111/php.12814. Epub 2017 Sep 15.

6.

Revisiting the value of competition assays in folate receptor-mediated drug delivery.

Jones SK, Sarkar A, Feldmann DP, Hoffmann P, Merkel OM.

Biomaterials. 2017 Sep;138:35-45. doi: 10.1016/j.biomaterials.2017.05.034. Epub 2017 May 22.

7.

The impact of microfluidic mixing of triblock micelleplexes on in vitro / in vivo gene silencing and intracellular trafficking.

Feldmann DP, Xie Y, Jones SK, Yu D, Moszczynska A, Merkel OM.

Nanotechnology. 2017 Jun 2;28(22):224001. doi: 10.1088/1361-6528/aa6d15. Epub 2017 May 10.

8.

Manipulation of small particles at solid liquid interface: light driven diffusioosmosis.

Feldmann D, Maduar SR, Santer M, Lomadze N, Vinogradova OI, Santer S.

Sci Rep. 2016 Nov 3;6:36443. doi: 10.1038/srep36443.

9.

Positive Effect of Reduced Activity and Bed Rest.

Feldmann D.

Dtsch Arztebl Int. 2016 Aug 22;113(33-34):562. doi: 10.3238/arztebl.2016.0562b. No abstract available.

10.

Light-Induced Reversible Change of Roughness and Thickness of Photosensitive Polymer Brushes.

Kopyshev A, Galvin CJ, Patil RR, Genzer J, Lomadze N, Feldmann D, Zakrevski J, Santer S.

ACS Appl Mater Interfaces. 2016 Jul 27;8(29):19175-84. doi: 10.1021/acsami.6b06881. Epub 2016 Jul 12.

PMID:
27351592
11.

The advantages of pulmonary delivery of therapeutic siRNA.

Feldmann DP, Merkel OM.

Ther Deliv. 2015;6(4):407-9. doi: 10.4155/tde.15.8. No abstract available.

PMID:
25996039
12.

Limits for antibiotic treatment set too narrow.

Feldmann D.

Dtsch Arztebl Int. 2014 Oct 31;111(44):757. doi: 10.3238/arztebl.2014.0757a. No abstract available.

13.

Comparison of single and two-tunnel techniques during open treatment of acromioclavicular joint disruption.

Hou Z, Graham J, Zhang Y, Strohecker K, Feldmann D, Bowen TR, Chen W, Smith W.

BMC Surg. 2014 Aug 15;14:53. doi: 10.1186/1471-2482-14-53.

14.

Bone marrow adipocytes promote tumor growth in bone via FABP4-dependent mechanisms.

Herroon MK, Rajagurubandara E, Hardaway AL, Powell K, Turchick A, Feldmann D, Podgorski I.

Oncotarget. 2013 Nov;4(11):2108-23.

15.

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.

Riahi Z, Hammami H, Ouragini H, Messai H, Zainine R, Bouyacoub Y, Romdhane L, Essaid D, Kefi R, Rhimi M, Bedoui M, Dhaouadi A, Feldmann D, Jonard L, Besbes G, Abdelhak S.

Gene. 2013 Aug 1;525(1):1-4. doi: 10.1016/j.gene.2013.04.078. Epub 2013 May 13.

PMID:
23680645
16.

CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.

Thauvin-Robinet C, Munck A, Huet F, de Becdelièvre A, Jimenez C, Lalau G, Gautier E, Rollet J, Flori J, Nové-Josserand R, Soufir JC, Haloun A, Hubert D, Houssin E, Bellis G, Rault G, David A, Janny L, Chiron R, Rives N, Hairion D, Collignon P, Valeri A, Karsenty G, Rossi A, Audrézet MP, Férec C, Leclerc J, Georges Md, Claustres M, Bienvenu T, Gérard B, Boisseau P, Cabet-Bey F, Cheillan D, Feldmann D, Clavel C, Bieth E, Iron A, Simon-Bouy B, Izard V, Steffann J, Viville S, Costa C, Drouineaud V, Fauque P, Binquet C, Bonithon-Kopp C, Morris MA, Faivre L, Goossens M, Roussey M, Girodon E; collaborating working group on p.Arg117His.

J Med Genet. 2013 Apr;50(4):220-7. doi: 10.1136/jmedgenet-2012-101427. Epub 2013 Feb 1.

PMID:
23378603
17.

[Analytical quality of assays and comparison of procedures for the sweat test].

Nguyen-Khoa T, Borgard JP, Marchand M, Sitruk-Khalfon D, Feuillet MN, Feldmann D, Vassault A, Rota M.

Ann Biol Clin (Paris). 2012 Jan-Feb;70(1):5-12. doi: 10.1684/abc.2011.0650. French.

18.

Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.

Gutiérrez Cortés N, Pertuiset C, Dumon E, Börlin M, Hebert-Chatelain E, Pierron D, Feldmann D, Jonard L, Marlin S, Letellier T, Rocher C.

Hum Mutat. 2012 Apr;33(4):681-9. doi: 10.1002/humu.22023. Epub 2012 Feb 14.

PMID:
22241583
19.

Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children.

Flamein F, Riffault L, Muselet-Charlier C, Pernelle J, Feldmann D, Jonard L, Durand-Schneider AM, Coulomb A, Maurice M, Nogee LM, Inagaki N, Amselem S, Dubus JC, Rigourd V, Brémont F, Marguet C, Brouard J, de Blic J, Clement A, Epaud R, Guillot L.

Hum Mol Genet. 2012 Feb 15;21(4):765-75. doi: 10.1093/hmg/ddr508. Epub 2011 Nov 7.

20.

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.

Bonnet C, Grati M, Marlin S, Levilliers J, Hardelin JP, Parodi M, Niasme-Grare M, Zelenika D, Délépine M, Feldmann D, Jonard L, El-Amraoui A, Weil D, Delobel B, Vincent C, Dollfus H, Eliot MM, David A, Calais C, Vigneron J, Montaut-Verient B, Bonneau D, Dubin J, Thauvin C, Duvillard A, Francannet C, Mom T, Lacombe D, Duriez F, Drouin-Garraud V, Thuillier-Obstoy MF, Sigaudy S, Frances AM, Collignon P, Challe G, Couderc R, Lathrop M, Sahel JA, Weissenbach J, Petit C, Denoyelle F.

Orphanet J Rare Dis. 2011 May 11;6:21. doi: 10.1186/1750-1172-6-21.

21.

Combined pulmonary fibrosis and emphysema syndrome associated with familial SFTPC mutation.

Cottin V, Reix P, Khouatra C, Thivolet-Béjui F, Feldmann D, Cordier JF.

Thorax. 2011 Oct;66(10):918-9. doi: 10.1136/thx.2010.151407. Epub 2011 Jan 19. No abstract available.

PMID:
21248320
22.

[French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening].

Sermet-Gaudelus I, Munck A, Rota M, Roussey M, Feldmann D, Nguyen-Khoa T; Groupe de travail "Dépistage néonatal" de la Fédération des centres de ressources et de compétences de la mucoviscidose.

Arch Pediatr. 2010 Sep;17(9):1349-58. doi: 10.1016/j.arcped.2010.06.021. Epub 2010 Aug 16. French. Erratum in: Arch Pediatr. 2010 Dec;17(12):1730. Nguyen-Khoa, T [added].

PMID:
20719482
23.

p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study.

René C, Paulet D, Girodon E, Costa C, Lalau G, Leclerc J, Cabet-Bey F, Bienvenu T, Blayau M, Iron A, Mittre H, Feldmann D, Guittard C, Claustres M, Georges Md.

Eur J Hum Genet. 2011 Jan;19(1):36-42. doi: 10.1038/ejhg.2010.137. Epub 2010 Aug 18.

24.

Surfactant protein C gene (SFTPC) mutation-associated lung disease: high-resolution computed tomography (HRCT) findings and its relation to histological analysis.

Mechri M, Epaud R, Emond S, Coulomb A, Jaubert F, Tarrant A, Feldmann D, Flamein F, Clement A, de Blic J, Taam RA, Brunelle F, le Pointe HD.

Pediatr Pulmonol. 2010 Oct;45(10):1021-9. doi: 10.1002/ppul.21289.

25.

Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct.

Jonard L, Niasme-Grare M, Bonnet C, Feldmann D, Rouillon I, Loundon N, Calais C, Catros H, David A, Dollfus H, Drouin-Garraud V, Duriez F, Eliot MM, Fellmann F, Francannet C, Gilbert-Dussardier B, Gohler C, Goizet C, Journel H, Mom T, Thuillier-Obstoy MF, Couderc R, Garabédian EN, Denoyelle F, Marlin S.

Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1049-53. doi: 10.1016/j.ijporl.2010.06.002.

PMID:
20621367
26.

Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form.

Sbidian E, Feldmann D, Bengoa J, Fraitag S, Abadie V, de Prost Y, Bodemer C, Hadj-Rabia S.

Clin Genet. 2010 Jun;77(6):587-92. doi: 10.1111/j.1399-0004.2009.01339.x. Epub 2010 Apr 14.

PMID:
20412116
27.

Characteristics of disorders associated with genetic mutations of surfactant protein C.

Thouvenin G, Abou Taam R, Flamein F, Guillot L, Le Bourgeois M, Reix P, Fayon M, Counil F, Depontbriand U, Feldmann D, Pointe HD, de Blic J, Clement A, Epaud R.

Arch Dis Child. 2010 Jun;95(6):449-54. doi: 10.1136/adc.2009.171553. Epub 2010 Apr 19.

PMID:
20403820
28.

Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!

Marlin S, Feldmann D, Nguyen Y, Rouillon I, Loundon N, Jonard L, Bonnet C, Couderc R, Garabedian EN, Petit C, Denoyelle F.

Biochem Biophys Res Commun. 2010 Apr 9;394(3):737-42. doi: 10.1016/j.bbrc.2010.03.062. Epub 2010 Mar 16.

PMID:
20230791
29.

NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome".

Guillot L, Carré A, Szinnai G, Castanet M, Tron E, Jaubert F, Broutin I, Counil F, Feldmann D, Clement A, Polak M, Epaud R.

Hum Mutat. 2010 Feb;31(2):E1146-62. doi: 10.1002/humu.21183.

PMID:
20020530
30.

Phenotype and genotype in females with POU3F4 mutations.

Marlin S, Moizard MP, David A, Chaissang N, Raynaud M, Jonard L, Feldmann D, Loundon N, Denoyelle F, Toutain A.

Clin Genet. 2009 Dec;76(6):558-63. doi: 10.1111/j.1399-0004.2009.01215.x.

PMID:
19930154
31.

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening.

Thauvin-Robinet C, Munck A, Huet F, Génin E, Bellis G, Gautier E, Audrézet MP, Férec C, Lalau G, Georges MD, Claustres M, Bienvenu T, Gérard B, Boisseau P, Cabet-Bey F, Feldmann D, Clavel C, Bieth E, Iron A, Simon-Bouy B, Costa C, Medina R, Leclerc J, Hubert D, Nové-Josserand R, Sermet-Gaudelus I, Rault G, Flori J, Leroy S, Wizla N, Bellon G, Haloun A, Perez-Martin S, d'Acremont G, Corvol H, Clément A, Houssin E, Binquet C, Bonithon-Kopp C, Alberti-Boulmé C, Morris MA, Faivre L, Goossens M, Roussey M; Collaborating Working Group on R117H, Girodon E.

J Med Genet. 2009 Nov;46(11):752-8. doi: 10.1136/jmg.2009.067215. Epub 2009 Jun 29.

PMID:
19880712
32.

[Genetic deafness in adults].

Marlin S, Jonard L, Feldmann D, Loundon N, Rouillon I, Couderc R, Denoyelle F.

Rev Prat. 2009 May 20;59(5):630-1. French. No abstract available.

PMID:
19552200
33.

New surfactant protein C gene mutations associated with diffuse lung disease.

Guillot L, Epaud R, Thouvenin G, Jonard L, Mohsni A, Couderc R, Counil F, de Blic J, Taam RA, Le Bourgeois M, Reix P, Flamein F, Clement A, Feldmann D.

J Med Genet. 2009 Jul;46(7):490-4. doi: 10.1136/jmg.2009.066829. Epub 2009 May 13. Erratum in: J Med Genet. 2010 Jul;47(7):485.

34.

Familial interstitial disease with I73T mutation: A mid- and long-term study.

Abou Taam R, Jaubert F, Emond S, Le Bourgeois M, Epaud R, Karila C, Feldmann D, Scheinmann P, de Blic J.

Pediatr Pulmonol. 2009 Feb;44(2):167-75. doi: 10.1002/ppul.20970.

PMID:
19148933
35.

A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss.

Feldmann D, Le Maréchal C, Jonard L, Thierry P, Czajka C, Couderc R, Ferec C, Denoyelle F, Marlin S, Fellmann F.

Eur J Med Genet. 2009 Jul-Aug;52(4):195-200. doi: 10.1016/j.ejmg.2008.11.006. Epub 2008 Dec 13.

PMID:
19101659
36.

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.

Hilgert N, Huentelman MJ, Thorburn AQ, Fransen E, Dieltjens N, Mueller-Malesinska M, Pollak A, Skorka A, Waligora J, Ploski R, Castorina P, Primignani P, Ambrosetti U, Murgia A, Orzan E, Pandya A, Arnos K, Norris V, Seeman P, Janousek P, Feldmann D, Marlin S, Denoyelle F, Nishimura CJ, Janecke A, Nekahm-Heis D, Martini A, Mennucci E, Tóth T, Sziklai I, Del Castillo I, Moreno F, Petersen MB, Iliadou V, Tekin M, Incesulu A, Nowakowska E, Bal J, Van de Heyning P, Roux AF, Blanchet C, Goizet C, Lancelot G, Fialho G, Caria H, Liu XZ, Xiaomei O, Govaerts P, Grønskov K, Hostmark K, Frei K, Dhooge I, Vlaeminck S, Kunstmann E, Van Laer L, Smith RJ, Van Camp G.

Eur J Hum Genet. 2009 Apr;17(4):517-24. doi: 10.1038/ejhg.2008.201. Epub 2008 Nov 5.

37.

Epitaxial ternary nitride thin films prepared by a chemical solution method.

Luo H, Wang H, Bi Z, Feldmann DM, Wang Y, Burrell AK, McCleskey TM, Bauer E, Hawley ME, Jia Q.

J Am Chem Soc. 2008 Nov 19;130(46):15224-5. doi: 10.1021/ja803544c. Epub 2008 Oct 22.

PMID:
18939844
38.

[Lung diseases associated with inherited disorders of surfactant metabolism].

Epaud R, Feldmann D, Guillot L, Clément A.

Arch Pediatr. 2008 Oct;15(10):1560-7. doi: 10.1016/j.arcped.2008.07.016. Epub 2008 Sep 19. French.

PMID:
18804975
39.

New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.

Pierron D, Rocher C, Amati-Bonneau P, Reynier P, Martin-Négrier ML, Allouche S, Batandier C, Mousson de Camaret B, Godinot C, Rotig A, Feldmann D, Bellanne-Chantelot C, Arveiler B, Pennarun E, Rossignol R, Crouzet M, Murail P, Thoraval D, Letellier T.

BMC Med Genet. 2008 May 7;9:41. doi: 10.1186/1471-2350-9-41.

40.

[Sweat testing: review of technical requirements].

Rota M, Nguyen-Khoa T, Marchand M, Feldmann D, Dumont J, Khalfon D, Vassault A, Borgard JP; Groupe de travail Test de la sueur du Collège national de biochimie des hôpitaux.

Ann Biol Clin (Paris). 2008 Mar-Apr;66(2):221-7. doi: 10.1684/abc.2008.0214. French.

41.

Perrault syndrome: report of four new cases, review and exclusion of candidate genes.

Marlin S, Lacombe D, Jonard L, Leboulanger N, Bonneau D, Goizet C, de Villemeur TB, Cabrol S, Houang M, Moatti L, Feldmann D, Denoyelle F.

Am J Med Genet A. 2008 Mar 1;146A(5):661-4. doi: 10.1002/ajmg.a.32180.

PMID:
18241061
42.

Occurrence, fate and assessment of polar metamizole (dipyrone) residues in hospital and municipal wastewater.

Feldmann DF, Zuehlke S, Heberer T.

Chemosphere. 2008 Apr;71(9):1754-64. doi: 10.1016/j.chemosphere.2007.11.032. Epub 2007 Dec 31.

PMID:
18164746
43.

A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E.

Jonard L, Feldmann D, Parsy C, Freitag S, Sinico M, Koval C, Grati M, Couderc R, Denoyelle F, Bodemer C, Marlin S, Hadj-Rabia S.

Eur J Med Genet. 2008 Jan-Feb;51(1):35-43. Epub 2007 Oct 4.

PMID:
18024254
44.

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.

Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF, Dollfus H, Eliot MM, Faivre L, Duvillard C, Couderc R, Garabedian EN, Petit C, Feldmann D, Denoyelle F.

Eur J Hum Genet. 2007 Nov;15(11):1145-55. Epub 2007 Jul 18.

45.

[The mutation 35delG of the gene of the connexin 26 is a frequent cause of autosomal-recessive non-syndromic hearing loss in Morocco].

Ratbi I, Hajji S, Ouldim K, Aboussair N, Feldmann D, Sefiani A.

Arch Pediatr. 2007 May;14(5):450-3. Epub 2007 Jan 16. French.

PMID:
17229560
46.

Association between two distinct executive tasks in schizophrenia: a functional transcranial Doppler sonography study.

Feldmann D, Schuepbach D, von Rickenbach B, Theodoridou A, Hell D.

BMC Psychiatry. 2006 May 24;6:25.

47.

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, Eliot MM, David A, Calais C, Drouin-Garraud V, Obstoy MF, Tran Ba Huy P, Lacombe D, Duriez F, Francannet C, Bitoun P, Petit C, Garabédian EN, Couderc R, Marlin S, Denoyelle F.

Eur J Hum Genet. 2006 Jun;14(6):773-9.

48.

GJB2 mutations and degree of hearing loss: a multicenter study.

Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, Wiszniewski W, Janecke AR, Nekahm-Heis D, Seeman P, Bendova O, Kenna MA, Frangulov A, Rehm HL, Tekin M, Incesulu A, Dahl HH, du Sart D, Jenkins L, Lucas D, Bitner-Glindzicz M, Avraham KB, Brownstein Z, del Castillo I, Moreno F, Blin N, Pfister M, Sziklai I, Toth T, Kelley PM, Cohn ES, Van Maldergem L, Hilbert P, Roux AF, Mondain M, Hoefsloot LH, Cremers CW, Löppönen T, Löppönen H, Parving A, Gronskov K, Schrijver I, Roberson J, Gualandi F, Martini A, Lina-Granade G, Pallares-Ruiz N, Correia C, Fialho G, Cryns K, Hilgert N, Van de Heyning P, Nishimura CJ, Smith RJ, Van Camp G.

Am J Hum Genet. 2005 Dec;77(6):945-57. Epub 2005 Oct 19.

49.

Mild cystic fibrosis revealed by persistent hyponatremia during the French 2003 heat wave, associated with the S1455X C-terminus CFTR mutation.

Epaud R, Girodon E, Corvol H, Niel F, Guigonis V, Clement A, Feldmann D, Bensman A, Ulinski T.

Clin Genet. 2005 Dec;68(6):552-3. No abstract available.

PMID:
16283887
50.

Results of cochlear implantation in two children with mutations in the OTOF gene.

Rouillon I, Marcolla A, Roux I, Marlin S, Feldmann D, Couderc R, Jonard L, Petit C, Denoyelle F, Garabédian EN, Loundon N.

Int J Pediatr Otorhinolaryngol. 2006 Apr;70(4):689-96. Epub 2005 Oct 13.

PMID:
16226319

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