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Results: 1 to 20 of 561

1.

Mouse tetrad analysis provides insights into recombination mechanisms and hotspot evolutionary dynamics.

Cole F, Baudat F, Grey C, Keeney S, de Massy B, Jasin M.

Nat Genet. 2014 Aug 24. doi: 10.1038/ng.3068. [Epub ahead of print]

PMID:
25151354
[PubMed - as supplied by publisher]
2.

Genotype-phenotype correlations for infants and children with ABCA3 deficiency.

Wambach JA, Casey AM, Fishman MP, Wegner DJ, Wert SE, Cole FS, Hamvas A, Nogee LM.

Am J Respir Crit Care Med. 2014 Jun 15;189(12):1538-43. doi: 10.1164/rccm.201402-0342OC.

PMID:
24871971
[PubMed - indexed for MEDLINE]
3.

Development, implementation, and dissemination of the I-PASS handoff curriculum: A multisite educational intervention to improve patient handoffs.

Starmer AJ, O'Toole JK, Rosenbluth G, Calaman S, Balmer D, West DC, Bale JF Jr, Yu CE, Noble EL, Tse LL, Srivastava R, Landrigan CP, Sectish TC, Spector ND; I-PASS Study Education Executive Committee.

Acad Med. 2014 Jun;89(6):876-84. doi: 10.1097/ACM.0000000000000264.

PMID:
24871238
[PubMed - indexed for MEDLINE]
4.

Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of alveolar capillary dysplasia with misalignment of pulmonary veins.

Szafranski P, Dharmadhikari AV, Wambach JA, Towe CT, White FV, Grady RM, Eghtesady P, Cole FS, Deutsch G, Sen P, Stankiewicz P.

Am J Med Genet A. 2014 Aug;164A(8):2013-9. doi: 10.1002/ajmg.a.36606. Epub 2014 May 19.

PMID:
24842713
[PubMed - in process]
Free PMC Article
5.

Placing faculty development front and center in a multisite educational initiative: lessons from the I-PASS Handoff study.

O'Toole JK, West DC, Starmer AJ, Yu CE, Calaman S, Rosenbluth G, Hepps JH, Lopreiato JO, Landrigan CP, Sectish TC, Spector ND; I-PASS Study Education Executive Committee.

Acad Pediatr. 2014 May-Jun;14(3):221-4. doi: 10.1016/j.acap.2014.02.013. No abstract available.

PMID:
24767774
[PubMed - in process]
6.

Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Heins HB, Druley TE, Mitra RD, Hamvas A, Cole FS.

J Pediatr. 2014 Jun;164(6):1316-21.e3. doi: 10.1016/j.jpeds.2014.02.021. Epub 2014 Mar 20.

PMID:
24657120
[PubMed - indexed for MEDLINE]
7.

The sense and sensibility of strand exchange in recombination homeostasis.

Cole F.

PLoS Genet. 2014 Jan;10(1):e1004104. doi: 10.1371/journal.pgen.1004104. Epub 2014 Jan 23. No abstract available.

PMID:
24465222
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype.

van Meel E, Wegner DJ, Cliften P, Willing MC, White FV, Kornfeld S, Cole FS.

BMC Med Genet. 2013 Oct 8;14:106. doi: 10.1186/1471-2350-14-106.

PMID:
24103465
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

The OHRP and SUPPORT.

Wilfond BS, Magnus D, Antommaria AH, Appelbaum P, Aschner J, Barrington KJ, Beauchamp T, Boss RD, Burke W, Caplan AL, Capron AM, Cho M, Clayton EW, Cole FS, Darlow BA, Diekema D, Faden RR, Feudtner C, Fins JJ, Fost NC, Frader J, Hester DM, Janvier A, Joffe S, Kahn J, Kass NE, Kodish E, Lantos JD, McCullough L, McKinney R Jr, Meadow W, O'Rourke PP, Powderly KE, Pursley DM, Ross LF, Sayeed S, Sharp RR, Sugarman J, Tarnow-Mordi WO, Taylor H, Tomlinson T, Truog RD, Unguru YT, Weise KL, Woodrum D, Youngner S.

N Engl J Med. 2013 Jun 20;368(25):e36. doi: 10.1056/NEJMc1307008. Epub 2013 Jun 5. No abstract available.

PMID:
23738513
[PubMed - indexed for MEDLINE]
Free Article
10.

Genetic variation in MKL2 and decreased downstream PCTAIRE1 expression in extreme, fatal primary human microcephaly.

Ramos EI, Bien-Willner GA, Li J, Hughes AE, Giacalone J, Chasnoff S, Kulkarni S, Parmacek M, Cole FS, Druley TE.

Clin Genet. 2014 May;85(5):423-32. doi: 10.1111/cge.12197. Epub 2013 Jun 18.

PMID:
23692340
[PubMed - in process]
Free PMC Article
11.

Congenital Lymphocytic Choriomeningitis Virus: When to Consider the Diagnosis.

Anderson JL, Levy PT, Leonard KB, Smyser CD, Tychsen L, Cole FS.

J Child Neurol. 2013 May 10;29(6):837-842. [Epub ahead of print]

PMID:
23666045
[PubMed - as supplied by publisher]
12.

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.

Sen P, Yang Y, Navarro C, Silva I, Szafranski P, Kolodziejska KE, Dharmadhikari AV, Mostafa H, Kozakewich H, Kearney D, Cahill JB, Whitt M, Bilic M, Margraf L, Charles A, Goldblatt J, Gibson K, Lantz PE, Garvin AJ, Petty J, Kiblawi Z, Zuppan C, McConkie-Rosell A, McDonald MT, Peterson-Carmichael SL, Gaede JT, Shivanna B, Schady D, Friedlich PS, Hays SR, Palafoll IV, Siebers-Renelt U, Bohring A, Finn LS, Siebert JR, Galambos C, Nguyen L, Riley M, Chassaing N, Vigouroux A, Rocha G, Fernandes S, Brumbaugh J, Roberts K, Ho-Ming L, Lo IF, Lam S, Gerychova R, Jezova M, Valaskova I, Fellmann F, Afshar K, Giannoni E, Muhlethaler V, Liang J, Beckmann JS, Lioy J, Deshmukh H, Srinivasan L, Swarr DT, Sloman M, Shaw-Smith C, van Loon RL, Hagman C, Sznajer Y, Barrea C, Galant C, Detaille T, Wambach JA, Cole FS, Hamvas A, Prince LS, Diderich KE, Brooks AS, Verdijk RM, Ravindranathan H, Sugo E, Mowat D, Baker ML, Langston C, Welty S, Stankiewicz P.

Hum Mutat. 2013 Jun;34(6):801-11. doi: 10.1002/humu.22313. Epub 2013 Apr 12.

PMID:
23505205
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1.

Hamvas A, Deterding RR, Wert SE, White FV, Dishop MK, Alfano DN, Halbower AC, Planer B, Stephan MJ, Uchida DA, Williames LD, Rosenfeld JA, Lebel RR, Young LR, Cole FS, Nogee LM.

Chest. 2013 Sep;144(3):794-804. doi: 10.1378/chest.12-2502.

PMID:
23430038
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Breaking the cycle: extending the persistent pain cycle diagram using an affective pictorial metaphor.

Stones C, Cole F.

Health Commun. 2014;29(1):32-40. doi: 10.1080/10410236.2012.715537. Epub 2013 Jan 28.

PMID:
23356651
[PubMed - in process]
15.

Levonorgestrel intrauterine system versus medical therapy for menorrhagia.

Gupta J, Kai J, Middleton L, Pattison H, Gray R, Daniels J; ECLIPSE Trial Collaborative Group.

N Engl J Med. 2013 Jan 10;368(2):128-37. doi: 10.1056/NEJMoa1204724.

PMID:
23301731
[PubMed - indexed for MEDLINE]
Free Article
16.

Duplication of 20p12.3 associated with familial Wolff-Parkinson-White syndrome.

Mills KI, Anderson J, Levy PT, Cole FS, Silva JN, Kulkarni S, Shinawi M.

Am J Med Genet A. 2013 Jan;161A(1):137-44. doi: 10.1002/ajmg.a.35701. Epub 2012 Dec 13.

PMID:
23239491
[PubMed - indexed for MEDLINE]
17.

Diagnosis of lung cancer: a bronchoscopist's perspective.

Griffin JP, Zaman MK, Niell HB, Tolley EA, Cole FH Jr, Weiman DS.

J Bronchology Interv Pulmonol. 2012 Jan;19(1):12-8. doi: 10.1097/LBR.0b013e3182425b5d.

PMID:
23207257
[PubMed - indexed for MEDLINE]
18.

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Depass K, Heins H, Druley TE, Mitra RD, An P, Zhang Q, Nogee LM, Cole FS, Hamvas A.

Pediatrics. 2012 Dec;130(6):e1575-82. doi: 10.1542/peds.2012-0918. Epub 2012 Nov 19.

PMID:
23166334
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Preaching about the converted: how meiotic gene conversion influences genomic diversity.

Cole F, Keeney S, Jasin M.

Ann N Y Acad Sci. 2012 Sep;1267:95-102. doi: 10.1111/j.1749-6632.2012.06595.x. Review.

PMID:
22954222
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Smoking cessation and serious mental illness: a service evaluation of a drop-in stop smoking clinic on an acute in-patient unit.

Robson D, Cole F, Jalasi S, Boojharut B, Smith S, Thompson S, Jones M, Haddad M.

J Clin Nurs. 2013 Feb;22(3-4):405-13. doi: 10.1111/j.1365-2702.2012.04222.x. Epub 2012 Sep 4.

PMID:
22946884
[PubMed - indexed for MEDLINE]

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