Effects of unsaturated fatty acid deprivation on neutral lipid synthesis in Saccharomyces cerevisiae.

מאת Buttke, T M, Pyle, A L
יצא לאור 1982

Defining functional groups, core structural features and inter-domain tertiary contacts essential for group II intron self-splicing: a NAIM analysis.

מאת Boudvillain, M, Pyle, A M
יצא לאור 1998

Branch-point attack in group II introns is a highly reversible transesterification, providing a potential proofreading mechanism for 5'-splice site selection.

מאת Chin, K, Pyle, A M
יצא לאור 1995

RNA binding activates RIG-I by releasing an autorepressed signaling domain

מאת Dickey, T. H., Song, B., Pyle, A. M.
הוצא לאור ב Sci Adv (2019)

A map of the binding site for catalytic domain 5 in the core of a group II intron ribozyme.

מאת Konforti, B B, Liu, Q, Pyle, A M
יצא לאור 1998

Direct measurement of oligonucleotide substrate binding to wild-type and mutant ribozymes from Tetrahymena.

מאת Pyle, A M, McSwiggen, J A, Cech, T R
יצא לאור 1990

High resolution footprinting of EcoRI and distamycin with Rh(phi)2(bpy)3+, a new photofootprinting reagent.

מאת Uchida, K, Pyle, A M, Morii, T, Barton, J K
יצא לאור 1989

Transcriptome analysis of human cumulus cells reveals hypoxia as the main determinant of follicular senescence

מאת Molinari, E., Bar, H., Pyle, A.M., Patrizio, P.
הוצא לאור ב Mol Hum Reprod (2016)

Analysis of putative RNase sensitivity and protease insensitivity of demethylation activity in extracts from rat myoblasts.

מאת Swisher, J F, Rand, E, Cedar, H, Marie Pyle, A
יצא לאור 1998

More than one way to splice an RNA: branching without a bulge and splicing without branching in group II introns.

מאת Chu, V T, Liu, Q, Podar, M, Perlman, P S, Pyle, A M
יצא לאור 1998

The DEAH-box protein PRP22 is an ATPase that mediates ATP-dependent mRNA release from the spliceosome and unwinds RNA duplexes.

מאת Wagner, J D, Jankowsky, E, Company, M, Pyle, A M, Abelson, J N
יצא לאור 1998

A common UCP2 polymorphism predisposes to stress hyperglycaemia in severe sepsis

מאת Pyle, A, Ibbett, I M, Gordon, C, Keers, S M, Walker, M, Chinnery, P F, Baudouin, S V
יצא לאור 2009

Generation of human induced pluripotent stem cells from dermal fibroblasts

מאת Lowry, W. E., Richter, L., Yachechko, R., Pyle, A. D., Tchieu, J., Sridharan, R., Clark, A. T., Plath, K.
יצא לאור 2008

Novel HSPB1 mutation causes both motor neuronopathy and distal myopathy

מאת Lewis-Smith, D.J., Duff, J., Pyle, A., Griffin, H., Polvikoski, T., Birchall, D., Horvath, R., Chinnery, P.F.
הוצא לאור ב Neurol Genet (2016)

A novel de novo STXBP1 mutation causes mitochondrial complex I deficiency and late onset juvenile onset parkinsonism

מאת Keogh, MJ, Daud, D, Pyle, A, Steele, H, Duff, J, Griffin, H, Taggart, S, Basu, AP, Taylor, R, Horvath, R, Ramesh, V, Chinnery, PF
הוצא לאור ב Neurogenetics (2015)

Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia

מאת Keogh, M. J., Steele, H., Douroudis, K., Pyle, A., Duff, J., Hussain, R., Smertenko, T., Griffin, H., Santibanez-Koref, M., Horvath, R., Chinnery, P. F.
הוצא לאור ב J Neurol (2015)

Episodic ataxia and hemiplegia caused by the 8993T→C mitochondrial DNA mutation

מאת Craig, K, Elliott, H R, Keers, S M, Lambert, C, Pyle, A, Graves, T D, Woodward, C, Sweeney, M G, Davis, M B, Hanna, M G, Chinnery, P F
יצא לאור 2007

Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution

מאת Voets, A.M., van den Bosch, B.J.C., Stassen, A.P., Hendrickx, A.T., Hellebrekers, D.M., Van Laer, L., Van Eyken, E., Van Camp, G., Pyle, A., Baudouin, S.V., Chinnery, P.F., Smeets, H.J.M.
יצא לאור 2011

Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease

מאת Boczonadi, V., King, M. S., Smith, A. C., Olahova, M., Bansagi, B., Roos, A., Eyassu, F., Borchers, C., Ramesh, V., Lochmüller, H., Polvikoski, T., Whittaker, R. G., Pyle, A., Griffin, H., Taylor, R. W., Chinnery, P. F., Robinson, A. J., Kunji, E. R. S., Horvath, R.
הוצא לאור ב Genet Med (2019)

Exome sequencing in dementia with Lewy bodies

מאת Keogh, M J, Kurzawa-Akanbi, M, Griffin, H, Douroudis, K, Ayers, K L, Hussein, R I, Hudson, G, Pyle, A, Cordell, H J, Attems, J, McKeith, I G, O'Brien, J T, Burn, D J, Morris, C M, Thomas, A J, Chinnery, P F
הוצא לאור ב Transl Psychiatry (2016)