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Items: 1 to 50 of 60

1.

Visualization of species pairwise associations: a case study of surrogacy in bird assemblages.

Lane PW, Lindenmayer DB, Barton PS, Blanchard W, Westgate MJ.

Ecol Evol. 2014 Aug;4(16):3279-89. doi: 10.1002/ece3.1182. Epub 2014 Jul 29.

2.

An empirical assessment of the focal species hypothesis.

Lindenmayer DB, Lane PW, Westgate MJ, Crane M, Michael D, Okada S, Barton PS.

Conserv Biol. 2014 Dec;28(6):1594-603. doi: 10.1111/cobi.12330. Epub 2014 Jul 21.

PMID:
25048948
3.

Global meta-analysis reveals low consistency of biodiversity congruence relationships.

Westgate MJ, Barton PS, Lane PW, Lindenmayer DB.

Nat Commun. 2014 May 21;5:3899. doi: 10.1038/ncomms4899.

PMID:
24844928
4.

An empirical assessment and comparison of species-based and habitat-based surrogates: a case study of forest vertebrates and large old trees.

Lindenmayer DB, Barton PS, Lane PW, Westgate MJ, McBurney L, Blair D, Gibbons P, Likens GE.

PLoS One. 2014 Feb 24;9(2):e89807. doi: 10.1371/journal.pone.0089807. eCollection 2014.

5.

A tool to assess the quality of a meta-analysis.

Higgins JP, Lane PW, Anagnostelis B, Anzures-Cabrera J, Baker NF, Cappelleri JC, Haughie S, Hollis S, Lewis SC, Moneuse P, Whitehead A.

Res Synth Methods. 2013 Dec;4(4):351-66. doi: 10.1002/jrsm.1092. Epub 2013 Oct 18.

PMID:
26053948
6.

Methodological quality of meta-analyses: matched-pairs comparison over time and between industry-sponsored and academic-sponsored reports.

Lane PW, Higgins JP, Anagnostelis B, Anzures-Cabrera J, Baker NF, Cappelleri JC, Haughie S, Hollis S, Lewis SC, Moneuse P, Whitehead A.

Res Synth Methods. 2013 Dec;4(4):342-50. doi: 10.1002/jrsm.1072. Epub 2013 Oct 18.

PMID:
26053947
7.

The efficacy and safety of retigabine and other adjunctive treatments for refractory partial epilepsy: a systematic review and indirect comparison.

Martyn-St James M, Glanville J, McCool R, Duffy S, Cooper J, Hugel P, Lane PW.

Seizure. 2012 Nov;21(9):665-78. doi: 10.1016/j.seizure.2012.07.011. Epub 2012 Aug 14. Review.

8.

Meta-analysis of incidence of rare events.

Lane PW.

Stat Methods Med Res. 2013 Apr;22(2):117-32. doi: 10.1177/0962280211432218. Epub 2012 Jan 4. Review.

PMID:
22218366
9.

Statistical approaches for conducting network meta-analysis in drug development.

Jones B, Roger J, Lane PW, Lawton A, Fletcher C, Cappelleri JC, Tate H, Moneuse P; PSI Health Technology Special Interest Group, Evidence Synthesis sub-team.

Pharm Stat. 2011 Nov-Dec;10(6):523-31. doi: 10.1002/pst.533.

PMID:
22213533
10.

Graphical approaches to the analysis of safety data from clinical trials.

Amit O, Heiberger RM, Lane PW.

Pharm Stat. 2008 Jan-Mar;7(1):20-35.

PMID:
17323410
11.

Analysis of exacerbation rates in asthma and chronic obstructive pulmonary disease: example from the TRISTAN study.

Keene ON, Jones MR, Lane PW, Anderson J.

Pharm Stat. 2007 Apr-Jun;6(2):89-97.

PMID:
17230434
12.

In collaboration: the Jackson Laboratory Craniofacial Resource.

Bauschatz JD, Curtain MM, Davisson MT, Lane PW, Donahue LR.

Crit Rev Eukaryot Gene Expr. 2003;13(2-4):107-8.

PMID:
14696959
13.

Multifactorial screening design and analysis of SELDI-TOF ProteinChip array optimization experiments.

Cordingley HC, Roberts SL, Tooke P, Armitage JR, Lane PW, Wu W, Wildsmith SE.

Biotechniques. 2003 Feb;34(2):364-5, 368-73.

14.

Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.

Johnson KR, Lane PW, Cook SA, Harris BS, Ward-Bailey PF, Bronson RT, Lyons BL, Shultz LD, Davisson MT.

Genomics. 2003 Jan;81(1):6-14.

PMID:
12573256
15.

Downeast anemia (dea), a new mouse model of severe nonspherocytic hemolytic anemia caused by hexokinase (HK(1)) deficiency.

Peters LL, Lane PW, Andersen SG, Gwynn B, Barker JE, Beutler E.

Blood Cells Mol Dis. 2001 Sep-Oct;27(5):850-60.

PMID:
11783948
16.

Maximization of signal derived from cDNA microarrays.

Wildsmith SE, Archer GE, Winkley AJ, Lane PW, Bugelski PJ.

Biotechniques. 2001 Jan;30(1):202-6, 208.

17.

Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.

Korobova O, Lane PW, Perry J, Palmer S, Ashworth A, Davisson MT, Arnheim N.

Genomics. 1998 Dec 15;54(3):556-9.

PMID:
9878259
18.

Juvenile bare: a new hair loss mutation on chromosome 7 of the mouse.

Lane PW, Bronson RT, Cook SA, Ward-Bailey P, Donahue LR, Davisson MT.

J Hered. 1998 May-Jun;89(3):254-7.

PMID:
9656467
19.

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.

Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, Faust JR.

Am J Med Genet. 1998 May 26;77(4):289-97.

PMID:
9600738
20.

Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac.

Johnson KR, Lane PW, Ward-Bailey P, Davisson MT.

Genomics. 1995 Sep 20;29(2):457-64.

PMID:
8666395
21.

Urogenital syndrome (us): a developmental mutation on chromosome 2 of the mouse.

Lane PW, Birkenmeier CS.

Mamm Genome. 1993 Sep;4(9):481-4.

PMID:
7906966
22.

Spontaneous renal artery thrombosis associated with altered mental status.

Campbell JP, Lane PW.

Ann Emerg Med. 1992 Dec;21(12):1505-7.

PMID:
1443852
23.

Rostral cerebellar malformation, (rcm): a new recessive mutation on chromosome 3 of the mouse.

Lane PW, Bronson RT, Spencer CA.

J Hered. 1992 Jul-Aug;83(4):315-8.

PMID:
1401878
24.

Hairpatches, a single gene mutation characterized by progressive renal disease and alopecia in the mouse. A potential model for a newly described heritable human disorder.

Shultz LD, Lane PW, Coman DR, Taylor S, Hall E, Lyons B, Wood BG, Schlager G.

Lab Invest. 1991 Nov;65(5):588-600.

PMID:
1836514
25.

Hydrocephalus with hop gait (hyh): a new mutation on chromosome 7 in the mouse.

Bronson RT, Lane PW.

Brain Res Dev Brain Res. 1990 Jun 1;54(1):131-6.

PMID:
2364541
26.
27.
28.

New mutation causing sterility in the mouse.

Handel MA, Lane PW, Schroeder AC, Davisson MT.

Gamete Res. 1988 Dec;21(4):409-23.

PMID:
3220432
29.

Spasmodic, a mutation on chromosome 11 in the mouse.

Lane PW, Ganser AL, Kerner AL, White WF.

J Hered. 1987 Nov-Dec;78(6):353-6.

PMID:
3429842
30.

Mouse models of genetic diseases.

Leiter EH, Beamer WG, Shultz LD, Barker JE, Lane PW.

Birth Defects Orig Artic Ser. 1987;23(3):221-57. Review. No abstract available.

PMID:
3307936
31.

Location of plucked (pk) on chromosome 18 of the mouse.

Lane PW, Eicher EM.

J Hered. 1985 Nov-Dec;76(6):476-7.

PMID:
4086792
32.

Osteosclerosis, a recessive skeletal mutation on chromosome 19 in the mouse.

Marks SC Jr, Seifert MF, Lane PW.

J Hered. 1985 May-Jun;76(3):171-6.

PMID:
3998439
33.

Anorexia, a recessive mutation causing starvation in preweanling mice.

Maltais LJ, Lane PW, Beamer WG.

J Hered. 1984 Nov-Dec;75(6):468-72.

PMID:
6595305
34.

Association of megacolon with a new dominant spotting gene (Dom) in the mouse.

Lane PW, Liu HM.

J Hered. 1984 Nov-Dec;75(6):435-9.

PMID:
6512238
35.

Not normal littermates.

Lane PW.

Science. 1982 Dec 10;218(4577):1070. No abstract available.

PMID:
17752847
36.

Vibrator (vb): a spinocerebellar system degeneration with autosomal recessive inheritance in mice.

Weimar WR, Lane PW, Sidman RL.

Brain Res. 1982 Nov 18;251(2):357-64.

PMID:
7139332
37.

Analysis of covariance and standardization as instances of prediction.

Lane PW, Nelder JA.

Biometrics. 1982 Sep;38(3):613-21.

PMID:
7171691
38.

Chromosome 18 of the house mouse.

Lane PW, Searle AG, Beechey CV, Eicher E.

J Hered. 1981 Nov-Dec;72(6):409-12.

PMID:
6949984
39.

Assignment of LH XVI to chromosome 3 in the mouse.

Eicher EM, Lane PW.

J Hered. 1980 Sep-Oct;71(5):315-8.

PMID:
6160178
40.

X-linked polydactyly (Xpl), a new mutation in the mouse.

Sweet HO, Lane PW.

J Hered. 1980 May-Jun;71(3):207-9.

PMID:
7391545
41.

Gene order in linkage group XVI of the house mouse.

Lane PW, Eicher EM.

J Hered. 1979 Jul-Aug;70(4):239-44.

PMID:
489953
42.

Myodystrophy, a new myopathy on chromosome 8 of the mouse.

Lane PW, Beamer TC, Myers DD.

J Hered. 1976 May-Jun;67(3):135-8.

PMID:
939913
43.

Osteopetrosis, a new recessive skeletal mutation on chromosome 12 of the mouse.

Marks SC Jr, Lane PW.

J Hered. 1976 Jan-Feb;67(1):11-18.

PMID:
1262696
44.

Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse.

Lane PW, Deol MS.

J Hered. 1974 Nov-Dec;65(6):362-4. No abstract available.

PMID:
4448900
45.

Chromosome 19 of the house mouse.

Lane PW, Eicher EM, Southard JL.

J Hered. 1974 Sep-Oct;65(5):297-300. No abstract available.

PMID:
4436535
46.
47.

The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL-KsJ and C57BL-6J strains.

Hummel KP, Coleman DL, Lane PW.

Biochem Genet. 1972 Aug;7(1):1-13. No abstract available.

PMID:
4557514
48.

Two new mutations in linkage group XVI of the house mouse. Flaky tail and varitint-waddler-J.

Lane PW.

J Hered. 1972 May-Jun;63(3):135-40. No abstract available.

PMID:
4557539
49.

Synovial rupture of shoulder joint.

Lane PW, Dyer NH, Hawkins CF.

Br Med J. 1972 Feb 5;1(5796):356. No abstract available.

50.

Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia, brachymorphic, and stubby.

Lane PW, Dickie MM.

J Hered. 1968 Sep-Oct;59(5):300-8. No abstract available.

PMID:
5713631

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