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Items: 33

1.

Longitudinal multi-omics of host-microbe dynamics in prediabetes.

Zhou W, Sailani MR, Contrepois K, Zhou Y, Ahadi S, Leopold SR, Zhang MJ, Rao V, Avina M, Mishra T, Johnson J, Lee-McMullen B, Chen S, Metwally AA, Tran TDB, Nguyen H, Zhou X, Albright B, Hong BY, Petersen L, Bautista E, Hanson B, Chen L, Spakowicz D, Bahmani A, Salins D, Leopold B, Ashland M, Dagan-Rosenfeld O, Rego S, Limcaoco P, Colbert E, Allister C, Perelman D, Craig C, Wei E, Chaib H, Hornburg D, Dunn J, Liang L, Rose SMS, Kukurba K, Piening B, Rost H, Tse D, McLaughlin T, Sodergren E, Weinstock GM, Snyder M.

Nature. 2019 May;569(7758):663-671. doi: 10.1038/s41586-019-1236-x. Epub 2019 May 29.

PMID:
31142858
2.

Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome.

Birgmeier J, Esplin ED, Jagadeesh KA, Guturu H, Wenger AM, Chaib H, Buckingham JA, Bejerano G, Bernstein JA.

Am J Med Genet A. 2018 Apr;176(4):1030-1036. doi: 10.1002/ajmg.a.38636.

PMID:
29575631
3.

Lipid profile, inflammation, and oxidative status in peri- and postmenopausal women.

Taleb-Belkadi O, Chaib H, Zemour L, Fatah A, Chafi B, Mekki K.

Gynecol Endocrinol. 2016 Dec;32(12):982-985. Epub 2016 Aug 25.

PMID:
27558905
4.

46,XY disorders of sex development and congenital diaphragmatic hernia: a case with dysmorphic facies, truncus arteriosus, bifid thymus, gut malrotation, rhizomelia, and adactyly.

Esplin ED, Chaib H, Haney M, Martin B, Homeyer M, Urban AE, Bernstein JA.

Am J Med Genet A. 2015 Jun;167(6):1360-4. doi: 10.1002/ajmg.a.37037. Epub 2015 Apr 21. Review.

5.

Genomic analysis of fibrolamellar hepatocellular carcinoma.

Xu L, Hazard FK, Zmoos AF, Jahchan N, Chaib H, Garfin PM, Rangaswami A, Snyder MP, Sage J.

Hum Mol Genet. 2015 Jan 1;24(1):50-63. doi: 10.1093/hmg/ddu418. Epub 2014 Aug 13.

6.

Clinical interpretation and implications of whole-genome sequencing.

Dewey FE, Grove ME, Pan C, Goldstein BA, Bernstein JA, Chaib H, Merker JD, Goldfeder RL, Enns GM, David SP, Pakdaman N, Ormond KE, Caleshu C, Kingham K, Klein TE, Whirl-Carrillo M, Sakamoto K, Wheeler MT, Butte AJ, Ford JM, Boxer L, Ioannidis JP, Yeung AC, Altman RB, Assimes TL, Snyder M, Ashley EA, Quertermous T.

JAMA. 2014 Mar 12;311(10):1035-45. doi: 10.1001/jama.2014.1717.

7.

Anti-leukemia activity of chaetocin via death receptor-dependent apoptosis and dual modulation of the histone methyl-transferase SUV39H1.

Chaib H, Nebbioso A, Prebet T, Castellano R, Garbit S, Restouin A, Vey N, Altucci L, Collette Y.

Leukemia. 2012 Apr;26(4):662-74. doi: 10.1038/leu.2011.271. Epub 2011 Oct 7.

PMID:
21979880
8.

[Histone methyltransferases: a new class of therapeutic targets in cancer treatment?].

Chaib H, Prébet T, Vey N, Collette Y.

Med Sci (Paris). 2011 Aug-Sep;27(8-9):725-32. doi: 10.1051/medsci/2011278014. Epub 2011 Aug 31. Review. French.

9.

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.

O'Toole JF, Liu Y, Davis EE, Westlake CJ, Attanasio M, Otto EA, Seelow D, Nurnberg G, Becker C, Nuutinen M, Kärppä M, Ignatius J, Uusimaa J, Pakanen S, Jaakkola E, van den Heuvel LP, Fehrenbach H, Wiggins R, Goyal M, Zhou W, Wolf MT, Wise E, Helou J, Allen SJ, Murga-Zamalloa CA, Ashraf S, Chaki M, Heeringa S, Chernin G, Hoskins BE, Chaib H, Gleeson J, Kusakabe T, Suzuki T, Isaac RE, Quarmby LM, Tennant B, Fujioka H, Tuominen H, Hassinen I, Lohi H, van Houten JL, Rotig A, Sayer JA, Rolinski B, Freisinger P, Madhavan SM, Herzer M, Madignier F, Prokisch H, Nurnberg P, Jackson PK, Khanna H, Katsanis N, Hildebrandt F.

J Clin Invest. 2010 Mar;120(3):791-802. doi: 10.1172/JCI40076. Epub 2010 Feb 22. Erratum in: J Clin Invest. 2010 Apr;120(4):1362. Jackson, Peter [corrected to Jackson, Peter K].

10.

Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24.

Ashraf S, Hoskins BE, Chaib H, Hoefele J, Pasch A, Saisawat P, Trefz F, Hacker HW, Nuernberg G, Nuernberg P, Otto EA, Hildebrandt F.

Nephrol Dial Transplant. 2010 May;25(5):1496-501. doi: 10.1093/ndt/gfp650. Epub 2009 Dec 10.

11.

A systematic approach to mapping recessive disease genes in individuals from outbred populations.

Hildebrandt F, Heeringa SF, Rüschendorf F, Attanasio M, Nürnberg G, Becker C, Seelow D, Huebner N, Chernin G, Vlangos CN, Zhou W, O'Toole JF, Hoskins BE, Wolf MT, Hinkes BG, Chaib H, Ashraf S, Schoeb DS, Ovunc B, Allen SJ, Vega-Warner V, Wise E, Harville HM, Lyons RH, Washburn J, Macdonald J, Nürnberg P, Otto EA.

PLoS Genet. 2009 Jan;5(1):e1000353. doi: 10.1371/journal.pgen.1000353. Epub 2009 Jan 23.

12.

Novel surface expression of reticulocalbin 1 on bone endothelial cells and human prostate cancer cells is regulated by TNF-alpha.

Cooper CR, Graves B, Pruitt F, Chaib H, Lynch JE, Cox AK, Sequeria L, van Golen KL, Evans A, Czymmek K, Bullard RS, Donald CD, Sol-Church K, Gendernalik JD, Weksler B, Farach-Carson MC, Macoska JA, Sikes RA, Pienta KJ.

J Cell Biochem. 2008 Aug 15;104(6):2298-309. doi: 10.1002/jcb.21785.

13.

Identification of BRAF as a new interactor of PLCepsilon1, the protein mutated in nephrotic syndrome type 3.

Chaib H, Hoskins BE, Ashraf S, Goyal M, Wiggins RC, Hildebrandt F.

Am J Physiol Renal Physiol. 2008 Jan;294(1):F93-9. Epub 2007 Oct 17.

14.

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible.

Hinkes B, Wiggins RC, Gbadegesin R, Vlangos CN, Seelow D, Nürnberg G, Garg P, Verma R, Chaib H, Hoskins BE, Ashraf S, Becker C, Hennies HC, Goyal M, Wharram BL, Schachter AD, Mudumana S, Drummond I, Kerjaschki D, Waldherr R, Dietrich A, Ozaltin F, Bakkaloglu A, Cleper R, Basel-Vanagaite L, Pohl M, Griebel M, Tsygin AN, Soylu A, Müller D, Sorli CS, Bunney TD, Katan M, Liu J, Attanasio M, O'toole JF, Hasselbacher K, Mucha B, Otto EA, Airik R, Kispert A, Kelley GG, Smrcka AV, Gudermann T, Holzman LB, Nürnberg P, Hildebrandt F.

Nat Genet. 2006 Dec;38(12):1397-405. Epub 2006 Nov 5.

PMID:
17086182
15.

Concordant copy number and transcriptional activity of genes mapping to derivative chromosomes 8 during cellular immortalization in vitro.

Begley L, Keeney D, Beheshti B, Squire JA, Kant R, Chaib H, MacDonald JW, Rhim J, Macoska JA.

Genes Chromosomes Cancer. 2006 Feb;45(2):136-46.

16.

Dielectric polarization and refractive indices of ultrathin barium titanate films on strontium titanate single crystals.

Chaib H, Eng LM, Otto T.

J Phys Condens Matter. 2005 Jan 12;17(1):161-79. doi: 10.1088/0953-8984/17/1/015. Epub 2004 Dec 10.

PMID:
21690676
17.

Evolution of 8p loss in transformed human prostate epithelial cells.

Macoska JA, Paris P, Collins C, Andaya A, Beheshti B, Chaib H, Kant R, Begley L, MacDonald JW, Squire JA.

Cancer Genet Cytogenet. 2004 Oct 1;154(1):36-43.

PMID:
15381370
18.

Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors.

Chaib H, MacDonald JW, Vessella RL, Washburn JG, Quinn JE, Odman A, Rubin MA, Macoska JA.

Genes Chromosomes Cancer. 2003 Jul;37(3):306-13.

19.
20.

Activated in prostate cancer: a PDZ domain-containing protein highly expressed in human primary prostate tumors.

Chaib H, Rubin MA, Mucci NR, Li L, Taylor JMG, Day ML, Rhim JS, Macoska JA.

Cancer Res. 2001 Mar 15;61(6):2390-4.

21.

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.

Adato A, Kalinski H, Weil D, Chaib H, Korostishevsky M, Bonne-Tamir B.

Am J Hum Genet. 1999 Jul;65(1):261-5. No abstract available.

22.

The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region.

Saouda M, Mansour A, Bou Moglabey Y, El Zir E, Mustapha M, Chaib H, Nehmé A, Mégarbané A, Loiselet J, Petit C, Slim R.

Hum Genet. 1998 Aug;103(2):193-8.

PMID:
9760205
23.

Connexin 26 gene linked to a dominant deafness.

Denoyelle F, Lina-Granade G, Plauchu H, Bruzzone R, Chaïb H, Lévi-Acobas F, Weil D, Petit C.

Nature. 1998 May 28;393(6683):319-20. No abstract available.

PMID:
9620796
24.

Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2).

Dodé C, Weil D, Levilliers J, Crozet F, Chaïb H, Levi-Acobas F, Guilford P, Petit C.

Genomics. 1998 Jan 1;47(1):125-30.

PMID:
9465305
25.

BOR and BO syndromes are allelic defects of EYA1.

Vincent C, Kalatzis V, Abdelhak S, Chaib H, Compain S, Helias J, Vaneecloo FM, Petit C.

Eur J Hum Genet. 1997 Jul-Aug;5(4):242-6.

PMID:
9359046
26.

Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.

Boulila-Elgaïed A, Masmoudi S, Drira M, Gouia M, Chaib H, Petit C, Ayadi H.

Arch Inst Pasteur Tunis. 1997 Jan-Apr;74(1-2):5-8.

PMID:
15945170
27.

A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21.

Chaïb H, Kaplan J, Gerber S, Vincent C, Ayadi H, Slim R, Munnich A, Weissenbach J, Petit C.

Hum Mol Genet. 1997 Jan;6(1):27-31.

PMID:
9002666
28.

Dietary (n-3) polyunsaturated fatty acids improve adipocyte insulin action and glucose metabolism in insulin-resistant rats: relation to membrane fatty acids.

Luo J, Rizkalla SW, Boillot J, Alamowitch C, Chaib H, Bruzzo F, Desplanque N, Dalix AM, Durand G, Slama G.

J Nutr. 1996 Aug;126(8):1951-8.

PMID:
8759367
29.

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

Chaib H, Place C, Salem N, Dodé C, Chardenoux S, Weissenbach J, el Zir E, Loiselet J, Petit C.

Hum Mol Genet. 1996 Jul;5(7):1061-4.

PMID:
8817348
30.

A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.

Chaïb H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselet J, Petit C.

Hum Mol Genet. 1996 Jan;5(1):155-8.

PMID:
8789454
31.

A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).

Guilford P, Dodé C, Crozet F, Blanchard S, Chaïb H, Levilliers J, Levi-Acobas F, Weil D, Weissenbach J, Cohen D, et al.

Genomics. 1995 Sep 1;29(1):163-9.

PMID:
8530067
32.

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.

Chaïb H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgon A, Petit C.

Hum Mol Genet. 1994 Dec;3(12):2219-22.

PMID:
7881423
33.

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C.

Hum Mol Genet. 1994 Jun;3(6):989-93.

PMID:
7951250

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