|
๐
|
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
12 auth.
A. Bender,
K. J. Krishnan,
C. Morris,
G. Taylor,
A. Reeve,
R. Perry,
...
E. Jaros,
J. Hersheson,
J. Betts,
T. Klopstock,
Robert W. Taylor,
D. Turnbull
|
10 |
2006 |
10
๐
|
|
๐ข
|
Mitochondrial DNA mutations in human disease
Laura C. Greaves,
Robert W. Taylor
|
10 |
2006 |
10
๐ข
|
|
๐ฆ
|
Mitochondrial DNA mutations in human disease
Robert W. Taylor,
D. Turnbull
|
9 |
2005 |
9
๐ฆ
|
|
๐
|
Recombinant Human Interleukin 1 Receptor Antagonist in the Treatment of Patients With Sepsis Syndrome: Results From a Randomized, Double-blind, Placebo-Controlled Trial
216 auth.
C. Fisher,
J. Dhainaut,
S. Opal,
J. Pribble,
R. Balk,
G. Slotman,
T. J. Iberti,
E. Rackow,
M. Shapiro,
R. Greenman,
H. Reines,
M. Shelly,
B. Thompson,
J. Labrecque,
M. Catalano,
...
W. Knaus,
J. Sadoff,
M. Astiz,
C. Carpati,
R. Bone,
B. Friedman,
A. J. Mure,
C. Brathwaite,
E. Shapiro,
L. Melhorn,
Robert W. Taylor,
M. Keegan,
Jacklyn OโBrien,
R. Schein,
M. Pena,
Monina Wasserlouf,
J. Oropello,
E. Benjamin,
R. Delguidice,
G. Emmanuel,
T. Lie,
L. Anderson,
J. Marshall,
W. D. Majo,
O. Rotstein,
D. Foster,
E. Abraham,
H. Middleton,
C. Perry,
H. Levy,
D. Fry,
S. Simpson,
R. Crowell,
M. Neidhart,
D. Stevens,
T. Coffman,
Nagraj Narasimhan,
D. K. Merrick,
W. Bergquist,
K. Matzel,
M. Huebler,
G. Foulke,
T. Albertson,
W. Walby,
R. Allen,
R. Baughman,
P. Hasselgren,
M. Fink,
F. Favorito,
B. Thompson,
R. Corbin,
G. Y. Shellhorse,
A. Frazier,
S. White,
C. Garrard,
C. A'Court,
S. Storer,
D. Gervich,
Debra Foshe,
R. Brase,
A. Bagdahn,
R. Cooney,
J. S. Smith,
Louis F. Martin,
J. Vincent,
G. Friedman,
G. Berlot,
J. Fletcher,
Mark D. Williams,
T. Wright,
Steven C. Johnson,
Carinda Feild,
K. Wolf,
N. MacIntyre,
H. Dubin,
M. Durkin,
Penelope K. Dubin,
K. Staubach,
A. Fein,
D. Schulman,
M. Niederman,
D. Chalfin,
P. A. Van,
Leeuwen,
M. Boermeester,
A. J. Schneider,
J. Bander,
Amy Imm,
G. Bernard,
L. Nelson,
M. Stroud,
K. Safcsak,
F. Cerra,
J. Rindal,
Henry Mann,
N. Halpern,
J. Silverstein,
M. Alicea,
W. Sibbald,
Claudio M. Martin,
F. Rutledge,
K. Petti,
J. Russell,
Robert Kruger,
Alana Drummond,
P. Lange,
T. Seifert,
A. Durocher,
A. Tenaillon,
R. Boiteau,
T. Lherm,
S. Lowry,
S. Coyle,
P. Barie,
E. DeMaria,
D. Snydman,
S. Schwaitzberg,
S. Nasraway,
J. Grindlinger,
W. Summer,
Benjamen de Boisblanc,
M. Wahl,
K. Alestig,
J. Grossman,
D. Maki,
H. Paz,
M. Weiner,
D. Bihari,
David Campbell,
G. Bleichner,
M. Dahn,
M. Lange,
Jesse B. Hall,
A. Pohlman,
R. Wenzel,
M. Grosserode,
M. Costigan,
W. Mileski,
J. Weigelt,
N. Yeston,
Cheryl Irizarry,
J. Ross,
J. Robbins,
P. Nightingale,
K. Owen,
S. Sandstedt,
S. Berg,
G. Simon,
M. Seneff,
K. Conry,
J. Zimmerman,
R. Dellinger,
R. F. Johnston,
Patricia Allee,
P. Grande,
E. Myhre,
J. Dhainaut,
I. Hamy,
J. Mira,
J. Harmon,
Jon C. White,
L. Mckie,
H. Silverman,
Pamela Tuma,
D. Bennett,
J. Porter,
M. Laurell,
S. Jacobs,
S. Ash,
D. Stiles,
M. Prior,
G. Knatterud,
M. Terrin,
J. Kufera,
Patricia Wilkens,
Knut Ra,
L. Monroe,
C. Sprung,
C. M. Hamilton,
R. Matthay,
W. McCabe,
J. Tonascia,
H. Wiedeman,
J. Wittes,
G. Campion,
C. R. Croft,
Richard Lustick,
J. Lookabaugh,
G. Gordon,
L. Noe,
D. Bloedow,
Smith Christopher,
Dennis Brannon,
R. Kush,
D. Ng,
E. Moore,
Karen Bazemore,
M. Galvan,
D. Wagner,
F. Harrell,
D. Stablein
|
9 |
1994 |
9
๐
|
|
๐
|
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease
13 auth.
G. Gorman,
A. Schaefer,
Y. Ng,
N. Gomez,
E. Blakely,
C. Alston,
C. Feeney,
R. Horvath,
P. Yu-Wai-Man,
P. Chinnery,
...
Robert W. Taylor,
D. Turnbull,
R. Mcfarland
|
9 |
2015 |
9
๐
|
|
๐ข
|
Mitochondrial DNA mutations and human disease.
H. Tuppen,
E. Blakely,
D. Turnbull,
Robert W. Taylor
|
9 |
2010 |
9
๐ข
|
|
๐
|
Prevalence of mitochondrial DNA disease in adults
8 auth.
A. Schaefer,
R. Mcfarland,
E. Blakely,
Langping He,
R. Whittaker,
Robert W. Taylor,
...
P. Chinnery,
D. Turnbull
|
9 |
2008 |
9
๐
|
|
๐ฆ
|
Mitochondrial DNA mutations in human colonic crypt stem cells.
12 auth.
Robert W. Taylor,
M. Barron,
G. Borthwick,
A. Gospel,
P. Chinnery,
D. Samuels,
...
G. Taylor,
S. Plusa,
S. Needham,
Laura C. Greaves,
T. Kirkwood,
D. Turnbull
|
9 |
2003 |
9
๐ฆ
|
|
๐ฆ
|
Low-dose inhaled nitric oxide in patients with acute lung injury: a randomized controlled trial.
9 auth.
Robert W. Taylor,
J. Zimmerman,
R. Dellinger,
R. Straube,
G. Criner,
K. Davis,
...
K. Kelly,
Thomas C. Smith,
R. Small
|
8 |
2004 |
8
๐ฆ
|
|
๐
|
Genetic diagnosis of Mendelian disorders via RNA sequencing
32 auth.
Laura S. Kremer,
Daniel M Bader,
Christian Mertes,
R. Kopajtich,
G. Pichler,
A. Iuso,
T. Haack,
E. Graf,
T. Schwarzmayr,
Caterina Terrile,
E. Koลaลรญkovรก,
B. Repp,
G. Kastenmรผller,
J. Adamski,
P. Lichtner,
...
Christoph Leonhardt,
B. Funalot,
A. Donati,
V. Tiranti,
A. Lombรจs,
C. Jardel,
D. Glรคser,
Robert W. Taylor,
D. Ghezzi,
J. Mayr,
A. Rรถtig,
P. Freisinger,
F. Distelmaier,
T. Strom,
T. Meitinger,
J. Gagneur,
H. Prokisch
|
8 |
2017 |
8
๐
|
|
๐ข
|
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.
14 auth.
G. Hudson,
P. AmatiโBonneau,
E. Blakely,
J. Stewart,
Langping He,
A. Schaefer,
P. Griffiths,
K. Ahlqvist,
A. Suomalainen,
P. Reynier,
...
R. Mcfarland,
D. Turnbull,
P. Chinnery,
Robert W. Taylor
|
8 |
2008 |
8
๐ข
|
|
๐
|
Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease
12 auth.
L. Craven,
H. Tuppen,
Gareth D. Greggains,
S. Harbottle,
J. Murphy,
Lynsey M Cree,
...
A. Murdoch,
P. Chinnery,
Robert W. Taylor,
R. Lightowlers,
M. Herbert,
D. Turnbull
|
8 |
2010 |
8
๐
|
|
๐ฌ
|
The epidemiology of mitochondrial disorders--past, present and future.
A. Schaefer,
Robert W. Taylor,
D. Turnbull,
P. Chinnery
|
8 |
2004 |
8
๐ฌ
|
