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1

Repeat-Associated Non-ATG Translation in Neurological Diseases

Zu, Tao, Pattamatta, Amrutha, Ranum, Laura P.W.

Journal:

Cold Spring Harbor Perspectives in Biology

Year:

2018

Language:

english

File:

PDF, 587 KB

english, 2018

2

Repeat associated non-ATG (RAN) translation

Cleary, John Douglas, Pattamatta, Amrutha, Ranum, Laura P. W.

Journal:

Journal of Biological Chemistry

Year:

2018

Language:

english

File:

PDF, 793 KB

english, 2018

3

RNA-MEDIATED NEUROMUSCULAR DISORDERS

Ranum, Laura P.W., Cooper, Thomas A.

Journal:

Annual Review of Neuroscience

Year:

2006

Language:

english

File:

PDF, 211 KB

english, 2006

4

All in the Family: Repeats and ALS/FTD

Pattamatta, Amrutha, Cleary, John D., Ranum, Laura P.W.

Journal:

Trends in Neurosciences

Year:

2018

Language:

english

File:

PDF, 826 KB

english, 2018

5

RAN Translation Regulated by Muscleblind Proteins in Myotonic Dystrophy Type 2

Zu, Tao, Cleary, John D., Liu, Yuanjing, Bañez-Coronel, Monica, Bubenik, Jodi L., Ayhan, Fatma, Ashizawa, Tetsuo, Xia, Guangbin, Clark, H. Brent, Yachnis, Anthony T., Swanson, Maurice S., Ranum, Laura

Journal:

Year:

2017

Language:

english

File:

PDF, 5.14 MB

english, 2017

6

Myotonic dystrophy: Clinical and molecular parallels between myotonic dystrophy type 1 and type 2

Laura P. W. Ranum, John W. Day

Journal:

Current Neurology and Neuroscience Reports

Year:

2002

Language:

english

File:

PDF, 414 KB

english, 2002

7

Isolation and Characterization of the Nitrate Reductase Structural Gene of Chlamydomonas reinhardtii

Emilio Fernández, Rogene Schnell, Laura P. W. Ranum, Susanne C. Hussey, Carolyn D. Silflow and Paul A. Lefebvre

Journal:

Proceedings of the National Academy of Sciences

Year:

1989

Language:

english

File:

PDF, 1003 KB

english, 1989

8

Double the Trouble: Bidirectional Expression of the SCA8 CAG/CTG Expansion Mutation -Evidence for RNA and Protein Gain of Function Effects

Ranum, Laura P.W., Daughters, Randy S., Tuttle, Daniel L., Gao, Wangcai, Ikeda, Yoshio, Moseley, Melinda L., Ebner, Tim, Swanson, Maurice S.

Journal:

Rinsho Shinkeigaku

Year:

2010

Language:

english

File:

PDF, 48 KB

english, 2010

9

Reply—

Moseley, Melinda L., Schut, Lawrence J., Bird, Thomas D., Day, John W., Ranum, Laura P.W.

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 94 KB

english, 2000

10

Mutagenic roles of DNA “repair” proteins in antibody diversity and disease-associated trinucleotide repeat instability

Meghan M. Slean, Gagan B. Panigrahi, Laura P. Ranum, Christopher E. Pearson

Journal:

Year:

2008

Language:

english

File:

PDF, 916 KB

english, 2008

11

Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes

Yoshio Ikeda, Randy S. Daughters, Laura P. W. Ranum

Journal:

Year:

2008

Language:

english

File:

PDF, 454 KB

english, 2008

12

Myotonic Dystrophy: RNA Pathogenesis Comes into Focus

Laura P.W. Ranum, John W. Day

Journal:

The American Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 278 KB

english, 2004

13

Mutational Origin of Machado-Joseph Disease in the Australian Aboriginal Communities of Groote Eylandt and Yirrkala

Martins, Sandra, Soong, Bing-Wen, Wong, Virginia C. N., Giunti, Paola, Stevanin, Giovanni, Ranum, Laura P. W., Sasaki, Hidenao, Riess, Olaf, Tsuji, Shoji, Coutinho, Paula, Amorim, António, Sequeiros,

Journal:

Archives of Neurology

Year:

2012

Language:

english

File:

PDF, 100 KB

english, 2012

14

Repeat-associated non-AUG (RAN) translation: insights from pathology

Banez-Coronel, Monica, Ranum, Laura P. W.

Journal:

Laboratory Investigation

Year:

2019

Language:

english

File:

PDF, 909 KB

english, 2019

15

Myotonic Dystrophy Type 2: Human Founder Haplotype and Evolutionary Conservation of the Repeat Tract

Christina L. Liquori, Yoshio Ikeda, Marcy Weatherspoon, Kenneth Ricker, Benedikt G.H. Schoser, Joline C. Dalton, John W. Day, Laura P.W. Ranum

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 1.06 MB

english, 2003

16

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11

Ranum, Laura P.W., Schut, Lawrence J., Lundgren, Julie K., Orr, Harry T., Livingston, Dennis M.

Journal:

Nature Genetics

Year:

1994

File:

PDF, 463 KB

1994

17

Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration inDrosophila

Damaris N. Lorenzo, Min-gang Li, Sarah E. Mische, Karen R. Armbrust, Laura P. W. Ranum and Thomas S. Hays

Journal:

The Journal of Cell Biology

Year:

2010

Language:

english

File:

PDF, 3.88 MB

english, 2010

18

Altered levels of the splicing factor muscleblind modifies cerebral cortical function in mouse models of myotonic dystrophy

Chen, Gang, Carter, Russell E., Cleary, John D., Reid, Tammy S., Ranum, Laura P., Swanson, Maurice S., Ebner, Timothy J.

Journal:

Neurobiology of Disease

Year:

2018

Language:

english

File:

PDF, 1.80 MB

english, 2018

19

A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking

Khare, Swati, Nick, Jerelyn A., Zhang, Yalan, Galeano, Kira, Butler, Brittany, Khoshbouei, Habibeh, Rayaprolu, Sruti, Hathorn, Tyisha, Ranum, Laura P. W., Smithson, Lisa, Golde, Todd E., Paucar, Marti

Journal:

Year:

2017

Language:

english

File:

PDF, 7.07 MB

english, 2017

20

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1

Orr, Harry T., Chung, Ming-yi, Banfi, Sandro, Kwiatkowski, Thomas J., Servadio, Antonio, Beaudet, Arthur L., McCall, Alanna E., Duvick, Lisa A., Ranum, Laura P. W., Zoghbi, Huda Y.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 824 KB

1993

21

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA

Koob, Michael D., Benzow, Kellie A., Bird, Thomas D., Day, John W., Moseley, Melinda L., Ranum, Laura P.W.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 590 KB

1998

22

NEUROPATHOLOGY OF A CASE OF SPINOCEREBELLAR ATAXIA TYPE 5 (SCA5) FROM THE LINCOLN KINDRED

Clark, H. Brent, Schut, Lawrence J., Ranum, Laura P. W.

Journal:

Journal of Neuropathology and Experimental Neurology

Year:

1998

File:

PDF, 114 KB

1998

23

New developments in RAN translation: insights from multiple diseases

Cleary, John Douglas, Ranum, Laura PW

Journal:

Current Opinion in Genetics & Development

Year:

2017

Language:

english

File:

PDF, 1.02 MB

english, 2017

24

Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)

John W Day, Robert Roelofs, Bonnie Leroy, Irene Pech, Kellie Benzow, Laura P.W Ranum

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 414 KB

english, 1999

25

Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype

Coenen, Marieke J H, Tieleman, Alide A, Schijvenaars, Mascha M V A P, Leferink, Maike, Ranum, Laura P W, Scheffer, Hans, van Engelen, Baziel G M

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 182 KB

english, 2011

26

Genome Modification Leads to Phenotype Reversal in Human Myotonic Dystrophy Type 1 Induced Pluripotent Stem Cell-Derived Neural Stem Cells

Xia, Guangbin, Gao, Yuanzheng, Jin, Shouguang, Subramony, S.H., Terada, Naohiro, Ranum, Laura P.W., Swanson, Maurice S., Ashizawa, Tetsuo

Journal:

Year:

2015

Language:

english

File:

PDF, 1.37 MB

english, 2015

27

RNA Gain-of-Function in Spinocerebellar Ataxia Type 8

Daughters, Randy S., Tuttle, Daniel L., Gao, Wangcai, Ikeda, Yoshio, Moseley, Melinda L., Ebner, Timothy J., Swanson, Maurice S., Ranum, Laura P. W., Pearson, Christopher E.

Journal:

Year:

2009

Language:

english

File:

PDF, 552 KB

english, 2009

28

Detection of Slipped-DNAs at the Trinucleotide Repeats of the Myotonic Dystrophy Type I Disease Locus in Patient Tissues

Axford, Michelle M., Wang, Yuh-Hwa, Nakamori, Masayuki, Zannis-Hadjopoulos, Maria, Thornton, Charles A., Pearson, Christopher E., Ranum, Laura P. W.

Journal:

Year:

2013

Language:

english

File:

PDF, 2.00 MB

english, 2013

29

NEUROPATHOLOGY OF A CASE OF SPINOCEREBELLAR ATAXIA TYPE 5 (SCA5) FROM THE LINCOLN KINDRED

Clark, H. Brent, Schut, Lawrence J., Ranum, Laura P. W.

Journal:

Journal of Neuropathology and Experimental Neurology

Year:

1998

File:

PDF, 114 KB

1998

30

Genetics and molecular pathogenesis of the myotonic dystrophies

John W. Day, Laura P. W. Ranum

Journal:

Current Neurology and Neuroscience Reports

Year:

2005

Language:

english

File:

PDF, 319 KB

english, 2005

31

10.1038/7710

Koob, Michael D., Ranum, Laura P.W., Moseley, Melinda L., Schut, Lawrence J., Benzow, Kellie A., Bird, Thomas D., Day, John W.

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 148 KB

english, 1999

32

Pathogenic RNA repeats: an expanding role in genetic disease

Laura P.W. Ranum, John W. Day

Journal:

Trends in Genetics

Year:

2004

Language:

english

File:

PDF, 146 KB

english, 2004

33

Hippocampal sclerosis dementia with the C9ORF72 hexanucleotide repeat expansion

Pletnikova, Olga, Sloane, Kelly L., Renton, Alan E., Traynor, Bryan J., Crain, Barbara J., Reid, Tammy, Zu, Tao, Ranum, Laura P.W., Troncoso, Juan C., Rabins, Peter V., Onyike, Chiadi U.

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 1.02 MB

english, 2014

34

Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients

Debra J. Maurer, Kellie A. Benzow, Lawrence J. Schut, Laura P.J. Ranum, Dennis M. Livingston

Journal:

Year:

1998

Language:

english

File:

PDF, 354 KB

english, 1998

35

Dominantly inherited, non-coding microsatellite expansion disorders

Laura P.W Ranum, John W Day

Journal:

Current Opinion in Genetics & Development

Year:

2002

Language:

english

File:

PDF, 71 KB

english, 2002

36

Extensive restriction fragment length polymorphisms in a new isolate ofChlamydomonas reinhardtii

Christian H. Gross, Laura P. W. Ranum, Paul A. Lefebvre

Journal:

Current Genetics

Year:

1988

Language:

english

File:

PDF, 697 KB

english, 1988

37

10.1038/570

Ranum, Laura P. W., Rasmussen, Paul F., Benzow, Kellie A., Koob, Michael D., Day, John W.

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 101 KB

english, 1998

38

Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood

Sznajder, Åukasz J., Scotti, Marina M., Shin, Jihae, Taylor, Katarzyna, Ivankovic, Franjo, Nutter, Curtis A., Aslam, Faaiq N., Subramony, S. H., Ranum, Laura P. W., Swanson, Maurice S.

Journal:

Nature Communications

Year:

2020

File:

PDF, 1.24 MB

2020

39

RNA pathogenesis of the myotonic dystrophies

John W. Day, Laura P.W. Ranum

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 287 KB

english, 2005

40

Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families

Tsukasa Saito, Yoshinobu Amakusa, Takashi Kimura, Osamu Yahara, Hitoshi Aizawa, Yoshio Ikeda, John W. Day, Laura P. W. Ranum, Kinji Ohno, Tohru Matsuura

Journal:

Year:

2008

Language:

english

File:

PDF, 117 KB

english, 2008

41

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I

Chung, Ming-yi, Ranum, Laura P.W., Duvick, Lisa A., Servadio, Antonio, Zoghbi, Huda Y., Orr, Harry T.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 698 KB

1993

42

Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders

Cleary, John Douglas, Ranum, Laura PW

Journal:

Current Opinion in Genetics & Development

Year:

2014

Language:

english

File:

PDF, 1.41 MB

english, 2014

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