inbetweener's genetics [30 articles] Export

Recent papers added to inbetweener's library classified by the tag genetics. You can also see everyone's genetics.

	Genetics of motor neuron disorders: new insights into pathogenic mechanisms [My Copy] Nature Reviews Genetics, Vol. 10, No. 11. (13 October 2009), pp. 769-782. by Patrick A. Dion, Hussein Daoud, Guy A. Rouleau posted to review motoneuron mnd genetics als by inbetweener on 2009-10-25 20:16:14 as along with 2 people psique bpcusack
	Evolution of the primate androgen receptor: a structural basis for disease. [My Copy] Journal of molecular evolution, Vol. 47, No. 3. (September 1998), pp. 334-342. by C. S. Choong, J. A. Kemppainen, E. M. Wilson posted to ar evolution genetics primates by inbetweener on 2009-05-06 17:28:33 as
	TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. [My Copy] Nature genetics, Vol. 40, No. 5. (30 May 2008), pp. 572-574. by Edor Kabashi, Paul N. Valdmanis, Patrick Dion, et al.Dan Spiegelman, Brendan J. McConkey, Christine Vande Velde, Jean-Pierre P. Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, Francois Salachas, Pierre-Francois F. Pradat, William Camu, Vincent Meininger, Nicolas Dupre, Guy A. Rouleau posted to als genetics tdp43 by inbetweener on 2009-04-13 02:01:46 as along with 2 people daforerog giovanni
	TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. [My Copy] Lancet neurology (4 April 2008) by Vivianna M M. Van Deerlin, James B B. Leverenz, Lynn M M. Bekris, et al.Thomas D D. Bird, Wuxing Yuan, Lauren B B. Elman, Dana Clay, Elisabeth McCarty M. Wood, Alice S S. Chen-Plotkin, Maria Martinez-Lage, Ellen Steinbart, Leo McCluskey, Murray Grossman, Manuela Neumann, I-Lin L. Wu, Wei-Shiung S. Yang, Robert Kalb, Douglas R R. Galasko, Thomas J J. Montine, John Q Q. Trojanowski, Virginia M-Y M. Lee, Gerard D D. Schellenberg, Chang-En E. Yu posted to als genetics tdp43 by inbetweener on 2009-04-13 01:57:08 as along with 1 person giovanni
	Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis. [My Copy] PLoS genetics, Vol. 4, No. 9. (2008) by N. J. Rutherford, Y. J. Zhang, M. Baker, et al.J. M. Gass, N. A. Finch, Y. F. Xu, H. Stewart, B. J. Kelley, K. Kuntz, R. J. Crook, J. Sreedharan, C. Vance, E. Sorenson, C. Lippa, E. H. Bigio, D. H. Geschwind, D. S. Knopman, H. Mitsumoto, R. C. Petersen, N. R. Cashman, M. Hutton, C. E. Shaw, K. B. Boylan, B. Boeve, N. R. Graff-Radford, Z. K. Wszolek, R. J. Caselli, D. W. Dickson, I. R. Mackenzie, L. Petrucelli, R. Rademakers posted to als genetics tdp43 by inbetweener on 2009-04-13 01:55:54 as
	TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. [My Copy] Science (New York, N.Y.), Vol. 319, No. 5870. (21 March 2008), pp. 1668-1672. by Jemeen Sreedharan, Ian P. Blair, Vineeta B. Tripathi, et al.Xun Hu, Caroline Vance, Boris Rogelj, Steven Ackerley, Jennifer C. Durnall, Kelly L. Williams, Emanuele Buratti, Francisco Baralle, Jacqueline de Belleroche, J. Douglas Mitchell, P. Nigel Leigh, Ammar Al-Chalabi, Christopher C. Miller, Garth Nicholson, Christopher E. Shaw posted to als genetics tdp43 by inbetweener on 2009-04-13 01:55:10 as along with 4 people StuartForrest daforerog giovanni davidlott
	TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis. [My Copy] PLoS ONE, Vol. 3, No. 6. (2008) by R. J. Guerreiro, J. C. Schymick, C. Crews, A. Singleton, J. Hardy, B. J. Traynor posted to als genetics tdp43 by inbetweener on 2009-04-13 01:54:51 as
	Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis [My Copy] Science, Vol. 323, No. 5918. (27 February 2009), pp. 1205-1208. by T. J. Kwiatkowski, D. A. Bosco, A. L. LeClerc, et al.E. Tamrazian, C. R. Vanderburg, C. Russ, A. Davis, J. Gilchrist, E. J. Kasarskis, T. Munsat, P. Valdmanis, G. A. Rouleau, B. A. Hosler, P. Cortelli, P. J. de Jong, Y. Yoshinaga, J. L. Haines, M. A. Pericak-Vance, J. Yan, N. Ticozzi, T. Siddique, D. McKenna-Yasek, P. C. Sapp, H. R. Horvitz, J. E. Landers, R. H. Brown posted to als clinical genetics rna by inbetweener on 2009-03-17 23:00:01 as along with 2 people StuartForrest daforerog
	The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12 [My Copy] Amyotrophic Lateral Sclerosis, Vol. 6, No. 2. (June 2005), pp. 111-114. by Achilli, Francesca, Boyle, et al. Shelagh, Kieran, Dairin, Chia, Ruth, Hafezparast, Majid, Martin, Joanne, Schiavo, Giampietro, Greensmith, Linda, Bickmore, Wendy, Fisher, Elizabeth posted to als genetics mouse sod1 by inbetweener on 2008-12-06 18:34:25 as
	Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions. [My Copy] Brain : a journal of neurology, Vol. 130, No. Pt 12. (December 2007), pp. 3265-3274. by D. Fialho, S. Schorge, U. Pucovska, et al.N. P. Davies, R. Labrum, A. Haworth, E. Stanley, R. Sud, W. Wakeling, M. B. Davis, D. M. Kullmann, M. G. Hanna posted to channel genetics myotonia by inbetweener on 2008-12-06 18:28:17 as
	Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals. [My Copy] J Neurol, Vol. 248, No. 1. (January 2001), pp. 23-26. by G. Kuhlenbäumer, W. Kress, E. B. Ringelstein, F. Stögbauer posted to ar genetics sbma by inbetweener on 2007-11-07 12:45:47 as
	The genetics of axonal transport and axonal transport disorders. [My Copy] PLoS Genet, Vol. 2, No. 9. (29 September 2006) by J. E. Duncan, L. S. Goldstein posted to axonaltransport geneticdisease genetics review by inbetweener on 2007-08-31 09:16:27 as
	Clinical features of the DOK7 neuromuscular junction synaptopathy. [My Copy] Brain, Vol. 130, No. Pt 6. (June 2007), pp. 1507-1515. by J. Palace, D. Lashley, J. Newsom-Davis, et al.J. Cossins, S. Maxwell, R. Kennett, S. Jayawant, Y. Yamanashi, D. Beeson posted to genetics myasthenia nmj phenotype by inbetweener on 2007-06-25 13:44:33 as
	Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes. [My Copy] Brain (17 April 2007) by Juliane S S. Müller, Agnes Herczegfalvi, Juan J J. Vilchez, et al.Jaume Colomer, Linda L L. Bachinski, Violeta Mihaylova, Manuela Santos, Ulrike Schara, Marcus Deschauer, Michael Shevell, Chantal Poulin, Ana Dias, Ana Soudo, Marja Hietala, Tuula Aärimaa, Ralf Krahe, Veronika Karcagi, Angela Huebner, David Beeson, Angela Abicht, Hanns Lochmüller posted to genetics myasthenia nmj phenotype by inbetweener on 2007-06-25 13:37:36 as along with 1 person mfrenkian
	Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy. [My Copy] Science (17 August 2006) by David Beeson, Osamu Higuchi, Jackie Palace, et al.Judy Cossins, Hayley Spearman, Susan Maxwell, John Newsom-Davis, Georgina Burke, Peter Fawcett, Masakatsu Motomura, Juliane S S. Müller, Hanns Lochmüller, Clarke Slater, Angela Vincent, Yuji Yamanashi posted to genetics myasthenia nmj by inbetweener on 2007-06-12 03:54:24 as along with 1 person kochhan
	Current understanding of congenital myasthenic syndromes [My Copy] Current Opinion in Pharmacology In Respiratory / Musculoskeletal, Vol. 5, No. 3. (June 2005), pp. 308-321. by Andrew G. Engel, Steven M. Sine posted to clinical genetics myasthenia neurology neuromuscular nmj by inbetweener on 2007-06-12 03:47:07 as
	Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. [My Copy] Science, Vol. 264, No. 5166. (17 June 1994), pp. 1772-1775. by M. E. Gurney, H. Pu, A. Y. Chiu, et al.M. C. Dal Canto, C. Y. Polchow, D. D. Alexander, J. Caliendo, A. Hentati, Y. W. Kwon, H. X. Deng posted to als genetics model mouse by inbetweener on 2006-10-09 21:43:54 as
	Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis [My Copy] Nature, Vol. 362, No. 6415. (4 March 1993), pp. 59-62. by Daniel R. Rosen, Teepu Siddique, David Patterson, et al.Denise A. Figlewicz, Peter Sapp, Afif Hentati, Deirdre Donaldson, Jun Goto, Jeremiah P. O'Regan, Han-Xiang Deng, Zohra Rahmani, Aldis Krizus, Diane Mckenna-Yasek, Annarueber Cayabyab, Sandra M. Gaston, Ralph Berger, Rudolph E. Tanzi, John J. Halperin, Brian Herzfeldt, Raymond V. den Bergh, Wu-Yen Hung, Thomas Bird, Gang Deng, Donald W. Mulder, Celestine Smyth, Nigel G. Laing, Edwin Soriano, Margaret A. Pericak-Vance, Jonathan Haines, Guy A. Rouleau, James S. Gusella, Robert H. Horvitz, Robert H. Brown posted to als genetics by inbetweener on 2006-10-09 21:39:25 as along with 1 person daforerog
	Molecular biology of amyotrophic lateral sclerosis: insights from genetics. [My Copy] Nature reviews. Neuroscience, Vol. 7, No. 9. (September 2006), pp. 710-723. by Piera Pasinelli, Robert H. Brown posted to als genetics molecularbiology pathogenesis pdf review by inbetweener on 2006-09-14 19:20:17 as along with 1 person Oyinlola
	The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size. [My Copy] Am J Hum Genet, Vol. 60, No. 5. (May 1997), pp. 1202-1210. by R. R. Brinkman, M. M. Mezei, J. Theilmann, E. Almqvist, M. R. Hayden posted to clinical genetics hd by inbetweener on 2006-09-14 18:02:56 as
	Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world. [My Copy] Eur J Hum Genet, Vol. 9, No. 6. (June 2001), pp. 431-436. by A. Lund, B. Udd, V. Juvonen, et al.P. M. Andersen, K. Cederquist, M. Davis, C. Gellera, C. Kölmel, L. O. Ronnevi, A. D. Sperfeld, S. A. Sörensen, L. Tranebjaerg, L. Van Maldergem, M. Watanabe, M. Weber, L. Yeung, M. L. Savontaus posted to ar genetics pdf sbma by inbetweener on 2006-04-03 18:47:18 as
	Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. [My Copy] PLoS Genet, Vol. 1, No. 3. (September 2005) by F. Yu, P. C. Sabeti, P. Hardenbol, et al.Q. Fu, B. Fry, X. Lu, S. Ghose, R. Vega, A. Perez, S. Pasternak, S. M. Leal, T. D. Willis, D. L. Nelson, J. Belmont, R. A. Gibbs posted to evolutionarybiology genetics pdf polyglutamine sca by inbetweener on 2006-04-03 18:09:48 as
	Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset. [My Copy] Brain (6 July 2005) by Stefan-M M. Pulst, Nieves Santos, Dai Wang, et al.Huiying Yang, Duong Huynh, Luis Velazquez, K Pattie P. Figueroa posted to clinical genetics polyglutamine sca by inbetweener on 2005-09-12 16:14:43 as
	PRENATAL DIAGNOSIS: An Earlier Look At Baby's Genes [My Copy] Science, Vol. 309, No. 5740. (02 September 2005), pp. 1476-1478. by Jocelyn Kaiser posted to clinical genetics by inbetweener on 2005-09-02 11:16:22 as
	Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. [My Copy] Nature, Vol. 352, No. 6330. (4 July 1991), pp. 77-79. by A. R. La Spada, E. M. Wilson, D. B. Lubahn, A. E. Harding, K. H. Fischbeck posted to ar clinical genetics polyglutamine sbma by inbetweener on 2005-08-08 19:34:48 as
	Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. [My Copy] Nat Genet, Vol. 2, No. 4. (December 1992), pp. 301-304. by A. R. La Spada, D. B. Roling, A. E. Harding, et al.C. L. Warner, R. Spiegel, I. Hausmanowa-Petrusewicz, W. C. Yee, K. H. Fischbeck posted to ar clinical genetics human sbma by inbetweener on 2005-08-08 19:33:27 as
	Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. [My Copy] Hum Mutat, Vol. 8, No. 1. (1996), pp. 32-37. by R. Spiegel, A. R. La Spada, W. Kress, K. H. Fischbeck, W. Schmid posted to ar genetics human sbma by inbetweener on 2005-08-08 19:32:52 as
	A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis. [My Copy] American journal of human genetics, Vol. 75, No. 5. (November 2004), pp. 822-831. by Agnes L. Nishimura, Miguel Mitne-Neto, Helga C. Silva, et al.Antônio Richieri-Costa, Susan Middleton, Duilio Cascio, Fernando Kok, João R. Oliveira, Tom Gillingwater, Jeanette Webb, Paul Skehel, Mayana Zatz posted to als genetics by inbetweener on 2005-08-08 18:26:46 as along with 3 people StuartForrest daforerog preeder
	Complex genetics of amyotrophic lateral sclerosis. [My Copy] Am J Hum Genet, Vol. 75, No. 6. (December 2004), pp. 933-947. by C. B. Kunst posted to als genetics populationgenetics by inbetweener on 2005-08-08 18:05:33 as along with 1 person preeder
	DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). [My Copy] Am J Hum Genet, Vol. 74, No. 6. (June 2004), pp. 1128-1135. by Y. Z. Chen, C. L. Bennett, H. M. Huynh, et al.I. P. Blair, I. Puls, J. Irobi, I. Dierick, A. Abel, M. L. Kennerson, B. A. Rabin, G. A. Nicholson, M. Auer-Grumbach, K. Wagner, P. De Jonghe, J. W. Griffin, K. H. Fischbeck, V. Timmerman, D. R. Cornblath, P. F. Chance posted to als genetics by inbetweener on 2005-08-08 17:43:39 as along with 2 people daforerog preeder

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review	120
ar	116
sbma	86
als	81
mouse	77
motoneuron	74
polyglutamine	68
axonaltransport	56
aggregation	55
heatshock	48
clinical	47
hd	45
therapy	43
neurodegeneration	37
cvcpaper	31
muscle	31
genetics	30
mitochondria	29
cellbiology	26
chaperones	26
pdf	21
transcription	20
cellculture	17
model	16
nmj	16
dynein	15
autophagy	14
calcium	14
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tempreview	14
developmentalbiology	12
mnd	12
geneticdisease	11
loa	11
androgen	10
apoptosis	10
drosophila	10
howtoreadapaper	10
human	10
huntingtin	10
pathogenesis	10
sca	10
ups	10
growthfactors	9
inclusions	9
pathology	9
proteinfolding	9
rat	9
casereport	8
caspase	8
endocytosis	8
nerveinjury	8
neurofilament	7
neurology	7
retinitispigmentosa	7
rna	7
tetanus	7
ayeshapaper	6
comment	6
endocrinology	6
evolution	6
hsf1	6
microarray	6
sod	6
sod1	6
techniques	6
arimoclomol	5
celldeath	5
hdac	5
myasthenia	5
nucleus	5
physiology	5
proteindegradation	5
tdp43	5
trr-i	5
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glia	4
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folding	2
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hsf	2
htt	2
ibm	2
igf	2
inclusion	2
kinesin	2
laboratoryanimals	2
motorunit	2
mrs	2
myosin	2
myotonia	2
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er	1
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inbetweener's genetics [30 articles] Export

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