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Items: 1 to 50 of 87

1.

Prevalence of antibiotic resistance in Escherichia coli isolated from urine samples routinely referred by general practitioners in a large urban centre in south-west England.

Chin TL, MacGowan AP, Bowker KE, Elder F, Beck CR, McNulty C.

J Antimicrob Chemother. 2015 Jul;70(7):2167-9. doi: 10.1093/jac/dkv050. Epub 2015 Mar 11. No abstract available.

PMID:
25766735
2.

Molecular cytogenetic insights to the phylogenetic affinities of the giraffe (Giraffa camelopardalis) and pronghorn (Antilocapra americana).

Cernohorska H, Kubickova S, Kopecna O, Kulemzina AI, Perelman PL, Elder FF, Robinson TJ, Graphodatsky AS, Rubes J.

Chromosome Res. 2013 Aug;21(5):447-60. doi: 10.1007/s10577-013-9361-0. Epub 2013 Jul 30.

PMID:
23896647
3.

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.

Bhoj EJ, Ramos P, Baker LA, Garg V, Cost N, Nordenskjöld A, Elder FF, Bleyl SB, Bowles NE, Arrington CB, Delhomme B, Vanhoutteghem A, Djian P, Zinn AR.

Eur J Hum Genet. 2011 May;19(5):540-6. doi: 10.1038/ejhg.2010.245. Epub 2011 Feb 2. Erratum in: Eur J Hum Genet. 2012 Feb;20(2):249. Garg, Vidu [added].

4.

Patterns of chromosomal evolution in Sigmodon, evidence from whole chromosome paints.

Swier VJ, Bradley RD, Rens W, Elder FF, Baker RJ.

Cytogenet Genome Res. 2009;125(1):54-66. doi: 10.1159/000218747. Epub 2009 Jul 14.

5.

Differences in activity and phosphorylation of MAPK enzymes in esophageal squamous cells of GERD patients with and without Barrett's esophagus.

Zhang HY, Zhang X, Chen X, Thomas D, Hormi-Carver K, Elder F, Spechler SJ, Souza RF.

Am J Physiol Gastrointest Liver Physiol. 2008 Sep;295(3):G470-8. doi: 10.1152/ajpgi.90262.2008. Epub 2008 Jul 10.

6.

Cryptic chromosomal abnormalities identified in children with congenital heart disease.

Richards AA, Santos LJ, Nichols HA, Crider BP, Elder FF, Hauser NS, Zinn AR, Garg V.

Pediatr Res. 2008 Oct;64(4):358-63. doi: 10.1203/PDR.0b013e31818095d0.

PMID:
18535492
7.

Cognitive and motor development during childhood in boys with Klinefelter syndrome.

Ross JL, Roeltgen DP, Stefanatos G, Benecke R, Zeger MP, Kushner H, Ramos P, Elder FF, Zinn AR.

Am J Med Genet A. 2008 Mar 15;146A(6):708-19. doi: 10.1002/ajmg.a.32232.

PMID:
18266239
8.

Chromosomal evolution in tenrecs (Microgale and Oryzorictes, Tenrecidae) from the Central Highlands of Madagascar.

Gilbert C, Goodman SM, Soarimalala V, Olson LE, O'Brien PC, Elder FF, Yang F, Ferguson-Smith MA, Robinson TJ.

Chromosome Res. 2007;15(8):1075-91. Epub 2007 Nov 6.

PMID:
18058249
9.

Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.

Prieto JC, Garcia NM, Elder FF, Zinn AR, Baker LA.

J Pediatr Surg. 2007 Nov;42(11):1928-32.

PMID:
18022449
10.

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

Zinn AR, Roeltgen D, Stefanatos G, Ramos P, Elder FF, Kushner H, Kowal K, Ross JL.

Behav Brain Funct. 2007 May 21;3:24.

11.

Characterization of telomerase-immortalized, non-neoplastic, human Barrett's cell line (BAR-T).

Jaiswal KR, Morales CP, Feagins LA, Gandia KG, Zhang X, Zhang HY, Hormi-Carver K, Shen Y, Elder F, Ramirez RD, Sarosi GA Jr, Spechler SJ, Souza RF.

Dis Esophagus. 2007;20(3):256-64.

PMID:
17509124
12.

Chromosome painting among Proboscidea, Hyracoidea and Sirenia: support for Paenungulata (Afrotheria, Mammalia) but not Tethytheria.

Pardini AT, O'Brien PC, Fu B, Bonde RK, Elder FF, Ferguson-Smith MA, Yang F, Robinson TJ.

Proc Biol Sci. 2007 May 22;274(1615):1333-40.

13.

The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome.

Ross JL, Kowal K, Quigley CA, Blum WF, Cutler GB Jr, Crowe B, Hovanes K, Elder FF, Zinn AR.

J Pediatr. 2005 Oct;147(4):499-507.

PMID:
16227037
14.

Complete trisomy 1q with mosaic Y;1 translocation: a recurrent aneuploidy presenting diagnostic dilemmas.

Scheuerle A, Heller K, Elder F.

Am J Med Genet A. 2005 Oct 1;138A(2):166-70. Review.

PMID:
16152651
15.

Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome.

Ross JL, Samango-Sprouse C, Lahlou N, Kowal K, Elder FF, Zinn A.

Horm Res. 2005;64(1):39-45. Epub 2005 Aug 3.

PMID:
16088206
16.

Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.

Zinn AR, Ramos P, Elder FF, Kowal K, Samango-Sprouse C, Ross JL.

J Clin Endocrinol Metab. 2005 Sep;90(9):5041-6. Epub 2005 Jun 14.

PMID:
15956082
17.

Lagomorphs (rabbits, pikas and hares) do not use telomere-directed replicative aging in vitro.

Forsyth NR, Elder FF, Shay JW, Wright WE.

Mech Ageing Dev. 2005 Jun-Jul;126(6-7):685-91.

PMID:
15888323
18.

Best practice in the care of patients with a tracheostomy.

Bond P, Grant F, Coltart L, Elder F.

Nurs Times. 2003 Jul 29-Aug 4;99(30):24-5. Review.

PMID:
12961937
19.

Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3.

Robinson ML, Allen CE, Davy BE, Durfee WJ, Elder FF, Elliott CS, Harrison WR.

Mamm Genome. 2002 Nov;13(11):625-32.

PMID:
12461648
20.

Preconception and prenatal screening for cystic fibrosis.

Baskin LB, Wians FH Jr, Elder F.

MLO Med Lab Obs. 2002 Oct;34(10):8-12; quiz 14, 16. No abstract available.

PMID:
12385171
21.

Complete SHOX deficiency causes Langer mesomelic dysplasia.

Zinn AR, Wei F, Zhang L, Elder FF, Scott CI Jr, Marttila P, Ross JL.

Am J Med Genet. 2002 Jun 15;110(2):158-63.

PMID:
12116254
22.

exma: an X-linked insertional mutation that disrupts forebrain and eye development.

Cunningham D, Xiao Q, Chatterjee A, Sulik K, Juriloff D, Elder F, Harrison W, Schuster G, Overbeek PA, Herman GE.

Mamm Genome. 2002 Apr;13(4):179-85.

PMID:
11956759
23.

Phenotypes Associated with SHOX Deficiency.

Ross JL, Scott C Jr, Marttila P, Kowal K, Nass A, Papenhausen P, Abboudi J, Osterman L, Kushner H, Carter P, Ezaki M, Elder F, Wei F, Chen H, Zinn AR.

J Clin Endocrinol Metab. 2001 Dec;86(12):5674-80.

PMID:
11739418
25.

A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his father.

Wei F, Cheng S, Badie N, Elder F, Scott C Jr, Nicholson L, Ross JL, Zinn AR.

Am J Med Genet. 2001 Sep 1;102(4):353-8.

PMID:
11503163
26.

The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus.

Carrel T, Purandare SM, Harrison W, Elder F, Fox T, Casey B, Herman GE.

Hum Mol Genet. 2000 Aug 12;9(13):1937-42.

PMID:
10942421
27.

Mutations in a new photoreceptor-pineal gene on 17p cause leber congenital amaurosis. Nat gen 2000;24:79-83

Sohoki MM, Browne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Mehdi SQ, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP.

Am J Ophthalmol. 2000 Jun;129(6):834-5. No abstract available.

28.

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP.

Nat Genet. 2000 Jan;24(1):79-83.

29.

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome.

Lu W, Phillips CL, Killen PD, Hlaing T, Harrison WR, Elder FF, Miner JH, Overbeek PA, Meisler MH.

Genomics. 1999 Oct 15;61(2):113-24.

PMID:
10534397
31.

YAC rescue of downless locus mutations in mice.

Majumder K, Shawlot W, Schuster G, Harrison W, Elder FF, Overbeek PA.

Mamm Genome. 1998 Nov;9(11):863-8.

PMID:
9799834
32.

Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse.

Morgan D, Turnpenny L, Goodship J, Dai W, Majumder K, Matthews L, Gardner A, Schuster G, Vien L, Harrison W, Elder FF, Penman-Splitt M, Overbeek P, Strachan T.

Nat Genet. 1998 Oct;20(2):149-56. Erratum in: Nat Genet 1998 Nov;20(3):312.

PMID:
9771707
33.

A molecular cytogenetic analysis of X chromosome repatterning in the Bovidae: transpositions, inversions, and phylogenetic inference.

Robinson TJ, Harrison WR, Ponce de León FA, Davis SK, Elder FF.

Cytogenet Cell Genet. 1998;80(1-4):179-84.

PMID:
9678354
34.

Genomic DNA sequence, promoter expression, and chromosomal mapping of rat muscle carnitine palmitoyltransferase I.

Wang D, Harrison W, Buja LM, Elder FF, McMillin JB.

Genomics. 1998 Mar 15;48(3):314-23.

PMID:
9545636
35.

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Shapira SK, McCaskill C, Northrup H, Spikes AS, Elder FF, Sutton VR, Korenberg JR, Greenberg F, Shaffer LG.

Am J Hum Genet. 1997 Sep;61(3):642-50.

36.

Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites.

Sohocki MM, Sullivan LS, Harrison WR, Sodergren EJ, Elder FF, Weinstock G, Tanase S, Daiger SP.

Genomics. 1997 Mar 1;40(2):247-52.

PMID:
9119391
37.
38.

X chromosome evolution in the suni and eland antelope: detection of homologous regions by fluorescence in situ hybridization and G-banding.

Robinson TJ, Harrison WR, Ponce de León A, Elder FF.

Cytogenet Cell Genet. 1997;77(3-4):218-22.

PMID:
9284920
39.

Brachmann-de Lange syndrome: autosomal dominant inheritance and male-to-male transmission.

McKenney RR, Elder FF, Garcia J, Northrup H.

Am J Med Genet. 1996 Dec 30;66(4):449-52.

PMID:
8989466
40.

Characterization of human DSPG3, a small dermatan sulfate proteoglycan.

Deere M, Johnson J, Garza S, Harrison WR, Yoon SJ, Elder FF, Kucherlapati R, Hook M, Hecht JT.

Genomics. 1996 Dec 15;38(3):399-404.

PMID:
8975717
41.

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.

Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH.

Prenat Diagn. 1996 Apr;16(4):323-32.

PMID:
8734806
42.

Chromosomal evolution in duiker antelope (Cephalophinae: Bovidae): karyotype comparisons, fluorescence in situ hybridization, and rampant X chromosome variation.

Robinson TJ, Wilson V, Gallagher DS Jr, Taylor JF, Davis SK, Harrison WR, Elder FF.

Cytogenet Cell Genet. 1996;73(1-2):116-22.

PMID:
8646878
43.

Leukocyte adhesion deficiency mimicking Hirschsprung disease.

Rivera-Matos IR, Rakita RM, Mariscalco MM, Elder FF, Dreyer SA, Cleary TG.

J Pediatr. 1995 Nov;127(5):755-7. Review.

PMID:
7472832
44.

A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).

Hou J, Parrish J, Lüdecke HJ, Sapru M, Wang Y, Chen W, Hill A, Siegel-Bartelt J, Northrup H, Elder FF, et al.

Genomics. 1995 Sep 1;29(1):87-97.

PMID:
8530105
45.

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.

Hecht JT, Nelson LD, Crowder E, Wang Y, Elder FF, Harrison WR, Francomano CA, Prange CK, Lennon GG, Deere M, et al.

Nat Genet. 1995 Jul;10(3):325-9.

PMID:
7670471
46.

Cytogenetic characterization of three human and three rat medullary thyroid carcinoma cell lines.

Cooley LD, Elder FF, Knuth A, Gagel RF.

Cancer Genet Cytogenet. 1995 Apr;80(2):138-49.

PMID:
7736432
47.

Paracentric inversions in humans: a review of 446 paracentric inversions with presentation of 120 new cases.

Pettenati MJ, Rao PN, Phelan MC, Grass F, Rao KW, Cosper P, Carroll AJ, Elder F, Smith JL, Higgins MD, et al.

Am J Med Genet. 1995 Jan 16;55(2):171-87. Review.

PMID:
7717416
48.
49.

Reversal of left-right asymmetry: a situs inversus mutation.

Yokoyama T, Copeland NG, Jenkins NA, Montgomery CA, Elder FF, Overbeek PA.

Science. 1993 Apr 30;260(5108):679-82.

PMID:
8480178
50.

Bonus incentives can work in the business office.

Bernard MG, Elder F Jr.

Healthc Financ Manage. 1992 Jul;46(7):70, 72. No abstract available.

PMID:
10145654

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