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Results of search for 'au:"Lott, M"', page 3 of 5
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Authors
Beal, M F
Brown, M D
Chen, Y S
Corral-Debrinski, M
HUFFMAN, M N
Horton, T
Hose, G C
Hurlbut, D E
Hurley, B F
Katz, R J
LOTT, M H
Lott, M
Lott, M J
Lott, M T
Newman, N J
Power, M L
Shoffner, J M
Torroni, A
Voljavec, A S
Wallace, D C
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41.
Tracing the geographical origin of cocaine.
[electronic resource]
by
Ehleringer, J R
Casale, J F
Lott, M J
Ford, V L
Producer:
20001222
In:
Nature
vol. 408
Online resources:
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42.
Genetics and infection dynamics of Paratrichosoma sp in farmed saltwater crocodiles (Crocodylus porosus).
[electronic resource]
by
Lott, M J
Hose, G C
Isberg, S R
Power, M L
Producer:
20150825
In:
Parasitology research
vol. 114
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43.
Brush cytology in the diagnosis of neoplasia in Barrett's esophagus.
[electronic resource]
by
Hardwick, R H
Morgan, R J
Warren, B F
Lott, M
Alderson, D
Producer:
19980303
In:
Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus
vol. 10
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44.
Nematode community structure in the brush-tailed rock-wallaby, Petrogale penicillata: implications of captive breeding and the translocation of wildlife.
[electronic resource]
by
Lott, M J
Eldridge, M D B
Hose, G C
Power, M L
Producer:
20121128
In:
Experimental parasitology
vol. 132
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45.
[Therapeutic patient education in heart failure: a program's assessment].
[electronic resource]
by
Brunie, V
Lott, M-C
Guiader, J
Slama, M
Rieutord, A
Vignand-Courtin, C
Producer:
20120925
In:
Annales de cardiologie et d'angeiologie
vol. 61
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46.
Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
[electronic resource]
by
Brown, M D
Voljavec, A S
Lott, M T
MacDonald, I
Wallace, D C
Producer:
19920827
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
vol. 6
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47.
Tumour thickness in malignant melanoma: the limitations of frozen section.
[electronic resource]
by
Nield, D V
Saad, M N
Khoo, C T
Lott, M
Ali, M H
Producer:
19880901
In:
British journal of plastic surgery
vol. 41
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48.
Massive retroperitoneal lymphadenopathy as a terminal event in hairy cell leukaemia.
[electronic resource]
by
Mehta, A B
Catovsky, D
O'Brien, C J
Lott, M
Bowley, N
Hemmingway, A
Producer:
19840215
In:
Clinical and laboratory haematology
vol. 5
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49.
African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation Team.
[electronic resource]
by
Torroni, A
Brown, M D
Lott, M T
Newman, N J
Wallace, D C
Producer:
19950906
In:
Human mutation
vol. 5
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50.
Dynamic acousto-elastic test using continuous probe wave and transient vibration to investigate material nonlinearity.
[electronic resource]
by
Eiras, J N
Vu, Q A
Lott, M
Payá, J
Garnier, V
Payan, C
Producer:
20170518
In:
Ultrasonics
vol. 69
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51.
MITOMAP: a human mitochondrial genome database.
[electronic resource]
by
Kogelnik, A M
Lott, M T
Brown, M D
Navathe, S B
Wallace, D C
Producer:
19960410
In:
Nucleic acids research
vol. 24
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52.
MITOMAP: a human mitochondrial genome database--1998 update.
[electronic resource]
by
Kogelnik, A M
Lott, M T
Brown, M D
Navathe, S B
Wallace, D C
Producer:
19980218
In:
Nucleic acids research
vol. 26
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53.
Improving cytological diagnosis and surgical management of parotid adenolymphoma.
[electronic resource]
by
Lewis, D R
Webb, A J
Lott, M F
Brookes, S T
Farndon, J R
Producer:
19991122
In:
The British journal of surgery
vol. 86
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54.
MITOMAP: an update on the status of the human mitochondrial genome database.
[electronic resource]
by
Kogelnik, A M
Lott, M T
Brown, M D
Navathe, S B
Wallace, D C
Producer:
19970228
In:
Nucleic acids research
vol. 25
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55.
A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
[electronic resource]
by
Brown, M D
Yang, C C
Trounce, I
Torroni, A
Lott, M T
Wallace, D C
Producer:
19920901
In:
American journal of human genetics
vol. 51
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56.
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.
[electronic resource]
by
Corral-Debrinski, M
Stepien, G
Shoffner, J M
Lott, M T
Kanter, K
Wallace, D C
Producer:
19911017
In:
JAMA
vol. 266
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57.
mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.
[electronic resource]
by
Torroni, A
Lott, M T
Cabell, M F
Chen, Y S
Lavergne, L
Wallace, D C
Producer:
19941025
In:
American journal of human genetics
vol. 55
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58.
Three-dimensional modeling and numerical predictions of multimodal nonlinear behavior in damaged concrete blocks.
[electronic resource]
by
Lott, M
Payan, C
Garnier, V
Le Bas, P Y
Ulrich, T J
Remillieux, M C
Publication details:
The Journal of the Acoustical Society of America
Sep 2018
In:
The Journal of the Acoustical Society of America
vol. 144
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59.
Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.
[electronic resource]
by
Brown, M D
Torroni, A
Huoponen, K
Chen, Y S
Lott, M T
Wallace, D C
Producer:
19940815
In:
American journal of human genetics
vol. 55
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60.
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
[electronic resource]
by
Shoffner, J M
Lott, M T
Lezza, A M
Seibel, P
Ballinger, S W
Wallace, D C
Producer:
19900718
In:
Cell
vol. 61
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