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	STIM1 Mutation Associated with a Syndrome of Immunodeficiency and Autoimmunity [My Copy] N Engl J Med, Vol. 360, No. 19. (7 May 2009), pp. 1971-1980. by Capucine Picard, Christie-Ann Mccarl, Alexander Papolos, et al.Sara Khalil, Kevin Luthy, Claire Hivroz, Francoise Ledeist, Frederic Rieux-Laucat, Gideon Rechavi, Anjana Rao, Alain Fischer, Stefan Feske posted to autoimmunity clinical genetics_paper immunology by absterga on 2009-05-10 10:16:45 as along with 2 people djmonstermo jbhiatt
	Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome [My Copy] Cell, Vol. 65, No. 5. (31 May 1991), pp. 905-914. by A. Verkerk, M. Pieretti, J. Sutcliffe, et al.Y. Fu, D. Kuhl, A. Pizzuti, O. Reiner, S. Richards, M. Victoria, F. Zhang posted to genetics_paper by absterga on 2009-03-26 08:30:27 as
	Increased steady-state levels of CUGBP1 in myotonic dystrophy 1 are due to PKC-mediated hyperphosphorylation. [My Copy] Molecular cell, Vol. 28, No. 1. (12 October 2007), pp. 68-78. by N. M. Kuyumcu-Martinez, G. S. Wang, T. A. Cooper posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-26 00:22:47 as
	Low-dose metformin improves hyperglycaemia related to myotonic dystrophy [My Copy] Diabetic Medicine, Vol. 22, No. 3. (March 2005), pp. 346-347. by T. Kouki, N. Takasu, A. Nakachi, T. Tamanaha, I. Komiya, M. Tawata posted to genetics_paper read therapies by absterga on 2009-03-26 00:21:17 as
	Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy. [My Copy] The Journal of clinical investigation, Vol. 117, No. 12. (December 2007), pp. 3952-3957. by T. M. Wheeler, J. D. Lueck, M. S. Swanson, R. T. Dirksen, C. A. Thornton posted to genetics_paper read therapies by absterga on 2009-03-26 00:18:58 as
	Myotonic dystrophy: therapeutic strategies for the future. [My Copy] Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, Vol. 5, No. 4. (October 2008), pp. 592-600. by T. M. Wheeler posted to genetics_paper therapies by absterga on 2009-03-26 00:17:52 as
	Cytoplasmic and Nuclear Retained DMPK mRNAs Are Targets for RNA Interference in Myotonic Dystrophy Cells [My Copy] J. Biol. Chem., Vol. 280, No. 17. (29 April 2005), pp. 16949-16954. by Marc-Andre Langlois, Christelle Boniface, Gang Wang, et al.Jessica Alluin, Paul M. Salvaterra, Jack Puymirat, John J. Rossi, Nan S. Lee posted to genetics_paper therapies by absterga on 2009-03-26 00:15:19 as along with 1 person caizhiqiang
	Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy [My Copy] Nature Genetics, Vol. 38, No. 9. (30 July 2006), pp. 1066-1070. by Mani S. Mahadevan, Ramesh S. Yadava, Qing Yu, et al.Sadguna Balijepalli, Carla D. Frenzel-Mccardell, David T. Bourne, Lawrence H. Phillips posted to genetics_paper therapies by absterga on 2009-03-26 00:10:48 as
	Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy [My Copy] Hum. Mol. Genet., Vol. 14, No. 11. (1 June 2005), pp. 1539-1547. by Thai H. Ho, Donnie Bundman, Dawna L. Armstrong, Thomas A. Cooper posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-26 00:09:28 as
	The skeletal muscle chloride channel in dominant and recessive human myotonia [My Copy] Science, Vol. 257, No. 5071. (7 August 1992), pp. 797-800. by M. C. Koch, K. Steinmeyer, C. Lorenz, et al.K. Ricker, F. Wolf, M. Otto, B. Zoll, F. Lehmann-Horn, K. H. Grzeschik, T. J. Jentsch posted to genetics_paper read by absterga on 2009-03-25 01:21:13 as
	Muscleblind proteins regulate alternative splicing. [My Copy] The EMBO journal, Vol. 23, No. 15. (4 August 2004), pp. 3103-3112. by T. H. Ho, N. Charlet-B, M. G. Poulos, G. Singh, M. S. Swanson, T. A. Cooper posted to genetics_paper muscleblind read by absterga on 2009-03-24 20:47:12 as
	Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy [My Copy] Nat Genet, Vol. 25, No. 1. (May 2000), pp. 105-109. by Todd R. Klesert, Diane H. Cho, John I. Clark, et al.James Maylie, John Adelman, Lauren Snider, Eric C. Yuen, Philippe Soriano, Stephen J. Tapscott posted to genetics_paper read by absterga on 2009-03-24 18:10:13 as
	Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts [My Copy] Nat Genet, Vol. 25, No. 1. (May 2000), pp. 110-114. by Partha S. Sarkar, Binoy Appukuttan, Jennifer Han, et al.Yoshihiro Ito, Cuiwei Ai, Wenli Tsai, Yang Chai, Timothy J. Stout, Sita Reddy posted to genetics_paper read by absterga on 2009-03-24 18:09:28 as
	Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene [My Copy] Nat Genet, Vol. 16, No. 4. (August 1997), pp. 407-409. by Charles A. Thornton, James P. Wymer, Zachary Simmons, Carolyn Mcclain, Richard T. Moxley posted to genetics_paper read by absterga on 2009-03-24 18:05:04 as
	DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model. [My Copy] The Journal of clinical investigation, Vol. 103, No. 4. (February 1999) by C. I. Berul, C. T. Maguire, M. J. Aronovitz, et al.J. Greenwood, C. Miller, J. Gehrmann, D. Housman, M. E. Mendelsohn, S. Reddy posted to genetics_paper read by absterga on 2009-03-24 17:49:38 as
	Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. [My Copy] Science, Vol. 293 (2001), pp. 864-867. by C. L. Liquori, K. Ricker, M. L. Moseley, et al.J. F. Jacobsen, W. Kress, S. L. Naylor, J. W. Day, L. P. Ranum posted to genetics_paper read by absterga on 2009-03-24 06:14:58 as along with 2 people and 1 group thegoose2 tharris C. elegans / WormBase
	Expansion of a CUG trinucleotide repeat in the 3′ untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 94, No. 14. (8 July 1997), pp. 7388-7393. by Brigid M. Davis, Mila E. Mccurrach, Krishan L. Taneja, Robert H. Singer, David E. Housman posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-24 05:33:56 as
	Myotonic Dystrophy [My Copy] (1989) by Peter S. Harper posted to genetics_paper read by absterga on 2009-03-24 04:27:28 as
	Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy [My Copy] Proceedings of the National Academy of Sciences, Vol. 103, No. 31. (1 August 2006), pp. 11748-11753. by Rahul N. Kanadia, Jihae Shin, Yuan Yuan, et al.Stuart G. Beattie, Thurman M. Wheeler, Charles A. Thornton, Maurice S. Swanson posted to genetics_paper muscleblind read rna_gain_of_function by absterga on 2009-03-23 23:52:18 as
	Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy. [My Copy] Molecular cell, Vol. 10, No. 1. (July 2002), pp. 35-44. by A. Mankodi, M. P. Takahashi, H. Jiang, et al.C. L. Beck, W. J. Bowers, R. T. Moxley, S. C. Cannon, C. A. Thornton posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:49:11 as
	RNA Leaching of Transcription Factors Disrupts Transcription in Myotonic Dystrophy [My Copy] Science, Vol. 303, No. 5656. (16 January 2004), pp. 383-387. by A. Ebralidze, Y. Wang, V. Petkova, K. Ebralidse, R. P. Junghans posted to genetics_paper muscleblind read rna_gain_of_function by absterga on 2009-03-23 23:46:04 as along with 1 person jrjensen08
	Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons [My Copy] Human Molecular Genetics, Vol. 13, No. 24. (20 October 2004), 3079. by Hong Jiang, Ami Mankodi, Maurice S. Swanson, Richard T. Moxley, Charles A. Thornton posted to genetics_paper rna_gain_of_function next by absterga on 2009-03-23 23:44:01 as
	A Muscleblind Knockout Model for Myotonic Dystrophy [My Copy] Science, Vol. 302, No. 5652. (12 December 2003), pp. 1978-1980. by Rahul N. Kanadia, Karen A. Johnstone, Ami Mankodi, et al.Codrin Lungu, Charles A. Thornton, Douglas Esson, Adrian M. Timmers, William W. Hauswirth, Maurice S. Swanson posted to genetics_paper muscleblind read rna_gain_of_function by absterga on 2009-03-23 23:41:21 as
	Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 92, No. 12. (6 June 1995), pp. 5465-5469. by A. D. Otten, S. J. Tapscott posted to genetics_paper read structure by absterga on 2009-03-23 23:38:33 as
	Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy [My Copy] Hum. Mol. Genet., Vol. 5, No. 1. (1 January 1996), pp. 115-121. by L. T. Timchenko, N. A. Timchenko, C. T. Caskey, R. Roberts posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:35:11 as
	Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation [My Copy] Hum. Mol. Genet., Vol. 4, No. 4. (1 April 1995), pp. 599-606. by Jianzhou Wang, Elena Pegoraro, Elisabetta Menegazzo, et al.Massimo Gennarelli, Rita C. Hoop, Corrado Angelini, Eric P. Hoffman posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:29:50 as
	Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice. [My Copy] Nature genetics, Vol. 13, No. 3. (July 1996), pp. 316-324. by G. Jansen, P. J. Groenen, D. Bächner, et al.P. H. Jap, M. Coerwinkel, F. Oerlemans, W. van den Broek, B. Gohlsch, D. Pette, J. J. Plomp, P. C. Molenaar, M. G. Nederhoff, C. J. van Echteld, M. Dekker, A. Berns, H. Hameister, B. Wieringa posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:27:33 as
	Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy. [My Copy] The EMBO journal, Vol. 19, No. 17. (1 September 2000), pp. 4439-4448. by J. W. Miller, C. R. Urbinati, P. Teng-Umnuay, et al.M. G. Stenberg, B. J. Byrne, C. A. Thornton, M. S. Swanson posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:22:46 as
	Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy [My Copy] Nucl. Acids Res., Vol. 24, No. 22. (15 November 1996), pp. 4407-4414. by L. T. Timchenko, J. W. Miller, N. A. Timchenko, et al.D. R. Devore, K. V. Datar, L. Lin, R. Roberts, C. T. Caskey, M. S. Swanson posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:20:25 as
	Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy [My Copy] Nat Genet, Vol. 29, No. 1. (September 2001), pp. 40-47. by Rajesh S. Savkur, Anne V. Philips, Thomas A. Cooper posted to genetics_paper insulin read rna_gain_of_function by absterga on 2009-03-23 23:19:05 as
	Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy [My Copy] Science, Vol. 260, No. 5105. (9 April 1993), pp. 235-238. by Y. H. Fu, D. L. Friedman, S. Richards, et al.J. A. Pearlman, R. A. Gibbs, A. Pizzuti, T. Ashizawa, M. B. Perryman, G. Scarlato, R. G. Fenwick, Al Et posted to genetics_paper read by absterga on 2009-03-23 23:17:46 as
	Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy [My Copy] Nat Genet, Vol. 1, No. 3. (June 1992), pp. 192-195. by Catherine Tsilfidis, Alex E. Mackenzie, Gabrielle Mettler, Juana Barcelo, Robert G. Korneluk posted to genetics_paper read by absterga on 2009-03-23 23:16:48 as
	Myotonic Dystrophy in Transgenic Mice Expressing an Expanded CUG Repeat [My Copy] Science, Vol. 289, No. 5485. (8 September 2000), pp. 1769-1772. by Ami Mankodi, Eric Logigian, Linda Callahan, et al.Carolyn Mcclain, Robert White, Don Henderson, Matt Krym, Charles A. Thornton posted to genetics_paper read rna_gain_of_function by absterga on 2009-03-23 23:16:06 as
	Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP [My Copy] Nat Genet, Vol. 16, No. 4. (August 1997), pp. 402-406. by Todd R. Klesert, Anne D. Otten, Thomas D. Bird, Stephen J. Tapscott posted to genetics_paper read structure by absterga on 2009-03-23 23:14:41 as
	Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy [My Copy] Nat Genet, Vol. 13, No. 3. (July 1996), pp. 325-335. by Sita Reddy, Daniel B. Smith, Mark M. Rich, et al.John M. Leferovich, Patricia Reilly, Brigid M. Davis, Khoa Tran, Helen Rayburn, Roderick Bronson, Didier Cros, Rita J. Balice-Gordon, David Housman posted to genetics_paper mouse_knockout read by absterga on 2009-03-23 23:12:58 as
	Disruption of Splicing Regulated by a CUG-Binding Protein in Myotonic Dystrophy [My Copy] Science, Vol. 280, No. 5364. (1 May 1998), pp. 737-741. by Anne V. Philips, Lubov T. Timchenko, Thomas A. Cooper posted to genetics_paper read by absterga on 2009-03-23 23:11:46 as
	Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene [My Copy] Science, Vol. 255, No. 5049. (6 March 1992), pp. 1253-1255. by M. Mahadevan, C. Tsilfidis, L. Sabourin, et al.G. Shutler, C. Amemiya, G. Jansen, C. Neville, M. Narang, J. Barcelo, K. O'Hoy, Al Et posted to genetics_paper read by absterga on 2009-03-23 23:10:46 as
	An unstable triplet repeat in a gene related to myotonic muscular dystrophy [My Copy] Science, Vol. 255, No. 5049. (6 March 1992), pp. 1256-1258. by Y. H. Fu, A. Pizzuti, R. G. Fenwick, et al.J. King, S. Rajnarayan, P. W. Dunne, J. Dubel, G. A. Nasser, T. Ashizawa, P. de Jong, Al Et posted to genetics_paper read by absterga on 2009-03-23 23:09:50 as
	Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. [My Copy] Cell, Vol. 68, No. 4. (21 February 1992), pp. 799-808. by J. D. Brook, M. E. McCurrach, H. G. Harley, et al.A. J. Buckler, D. Church, H. Aburatani, K. Hunter, V. P. Stanton, J. P. Thirion, T. Hudson posted to genetics_paper read by absterga on 2009-03-23 23:09:08 as
	Post-transcriptional processing generates a diversity of 5[prime]-modified long and short RNAs [My Copy] Nature, No. 457. (19 February 2009), pp. 1028-1032. by Affymetrix/cold posted to genetics_paper mrna post_transcriptional_processing read by absterga on 2009-02-23 19:20:00 as

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read	161
clinical	112
case_reports	47
cancer	46
genetics_paper	40
zinc_finger	39
dna_protein_interactions	38
hematology	33
ewings_sarcoma	31
dna_binding_motif	30
genome_550	29
tf_project	27
massivly_parallel_sequencing	26
immunology	26
transcription_factors	25
cool_technique	24
paper	22
dnasei_hypersensitivity	20
neuro	19
nuclear_permeabilization	18
dna_methylation_protien-binding	17
structure	17
drug_discovery	16
dnasei	16
cardiac	16
rna_gain_of_function	15
ews-fli1	15
stem_cells	14
mass_spec	13
selex	13
mouse_knockout	12
mathamatical_modeling	12
histone_modifications	12
mutation	11
chromatin	11
psychiatry	11
mrna	11
k562	11
review	11
promoters	11
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hl-60	9
malignant_transformation	9
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endocrine	9
epigenetics	8
yeast	8
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renal	8
classic	8
transcription	7
therapies	7
protein_protein_interactions	7
chip-seq	7
platlets	7
dna_methylation	7
gi	7
ctcf	7
resistance	6
pulmonary	6
cnvs	5
virus	5
nejm	5
hiv	4
cellular_decisions	4
dna_binding_ms	4
evolution	4
unread	4
muscleblind	4
snp_chip	4
py	4
tuberculosis	4
mri	3
rbc	3
nmr	3
insulin	3
tissue_specificity	3
biomarker	3
dna_detection	3
diagnostic_testing	3
autoimmunity	3
cml	3
nucleosome	3
ptm	3
tregs	3
antibodies	3
genetic_disease	3
gene_therapy	3
adipose	3
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rna	2
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stress	2
microbes	2
ips	2
dermatology	2
global_warming	2
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bcl-2	2
reproduction	2
dna_demethylation	2
zebra_fish	2
ews-etv1	2
optics	2
dnaaei	2
polycomb	2
master_switches	2
enhancers	2
ews-erg	2
noise	2
cell_migration	1
gwa_study	1
apoptosis	1
immune	1
e_coli	1
beta_thalassemia	1
srm	1
not_finished	1
mouse	1
ph_domain	1
aging	1
scan_domain	1
cell_cycle	1
human_genetics	1
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post_transcriptional_processing	1
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scleroderma	1
book	1
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ace_levels	1
icat	1
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lad	1
ubiquitin	1
pet	1
dna_assembly	1
social_sciences	1
indel	1
phosphatase	1
cebpe	1
carbon_storage	1
functional_non_coding_regions	1
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sleep	1
th17	1
next	1
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dlbcl	1
bones	1
schizophrenia	1
mrna-seq	1
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