A citation-based method for searching scientific literature

U Suter, G J Snipes, R Schoener-Scott, A A Welcher, S Pareek, J R Lupski, R A Murphy, E M Shooter, P I Patel. J Biol Chem 1994
Times Cited: 170







List of co-cited articles
1021 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
J R Lupski, R M de Oca-Luna, S Slaugenhaupt, L Pentao, V Guzzetta, B J Trask, O Saucedo-Cardenas, D F Barker, J M Killian, C A Garcia,[...]. Cell 1991
44

DNA deletion associated with hereditary neuropathy with liability to pressure palsies.
P F Chance, M K Alderson, K A Leppig, M W Lensch, N Matsunami, B Smith, P D Swanson, S J Odelberg, C M Disteche, T D Bird. Cell 1993
675
42

Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13).
G J Snipes, U Suter, A A Welcher, E M Shooter. J Cell Biol 1992
336
36

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
P I Patel, B B Roa, A A Welcher, R Schoener-Scott, B J Trask, L Pentao, G J Snipes, C A Garcia, U Francke, E M Shooter,[...]. Nat Genet 1992
480
31

A myelin protein is encoded by the homologue of a growth arrest-specific gene.
A A Welcher, U Suter, M De Leon, G J Snipes, E M Shooter. Proc Natl Acad Sci U S A 1991
221
29

A growth arrest-specific (gas) gene codes for a membrane protein.
G Manfioletti, M E Ruaro, G Del Sal, L Philipson, C Schneider. Mol Cell Biol 1990
237
26

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A.
L J Valentijn, F Baas, R A Wolterman, J E Hoogendijk, N H van den Bosch, I Zorn, A W Gabreëls-Festen, M de Visser, P A Bolhuis. Nat Genet 1992
417
24

A transgenic rat model of Charcot-Marie-Tooth disease.
M Sereda, I Griffiths, A Pühlhofer, H Stewart, M J Rossner, F Zimmerman, J P Magyar, A Schneider, E Hund, H M Meinck,[...]. Neuron 1996
281
24


Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice.
K Adlkofer, R Martini, A Aguzzi, J Zielasek, K V Toyka, U Suter. Nat Genet 1995
298
22

Progesterone stimulates the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells.
F Désarnaud, A N Do Thi, A M Brown, G Lemke, U Suter, E E Baulieu, M Schumacher. J Neurochem 1998
138
22


Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage.
J P Magyar, R Martini, T Ruelicke, A Aguzzi, K Adlkofer, Z Dembic, J Zielasek, K V Toyka, U Suter. J Neurosci 1996
186
20

Trembler mouse carries a point mutation in a myelin gene.
U Suter, A A Welcher, T Ozcelik, G J Snipes, B Kosaras, U Francke, S Billings-Gagliardi, R L Sidman, E M Shooter. Nature 1992
382
20

Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene.
P Spreyer, G Kuhn, C O Hanemann, C Gillen, H Schaal, R Kuhn, G Lemke, H W Müller. EMBO J 1991
174
20

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study.
E Nelis, C Van Broeckhoven, P De Jonghe, A Löfgren, A Vandenberghe, P Latour, E Le Guern, A Brice, M L Mostacciuolo, F Schiavon,[...]. Eur J Hum Genet 1996
353
20

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies.
G A Nicholson, L J Valentijn, A K Cherryson, M L Kennerson, T L Bragg, R M DeKroon, D A Ross, J D Pollard, J G McLeod, P A Bolhuis. Nat Genet 1994
218
19


Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.
B B Roa, C A Garcia, U Suter, D A Kulpa, C A Wise, J Mueller, A A Welcher, G J Snipes, E M Shooter, P I Patel,[...]. N Engl J Med 1993
327
18

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.
C Huxley, E Passage, A Manson, G Putzu, D Figarella-Branger, J F Pellissier, M Fontés. Hum Mol Genet 1996
177
18

Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).
Michael W Sereda, Gerd Meyer zu Hörste, Ueli Suter, Naureen Uzma, Klaus-Armin Nave. Nat Med 2003
203
18

Peripheral myelin protein-22 is expressed in rat and mouse brain and spinal cord motoneurons.
E Parmantier, F Cabon, C Braun, D D'Urso, H W Müller, B Zalc. Eur J Neurosci 1995
76
22



A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.
P Young, H Wiebusch, F Stögbauer, B Ringelstein, G Assmann, H Funke. Neurology 1997
71
21

Krox-20 controls myelination in the peripheral nervous system.
P Topilko, S Schneider-Maunoury, G Levi, A Baron-Van Evercooren, A B Chennoufi, T Seitanidou, C Babinet, P Charnay. Nature 1994
606
15

Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells.
S Pareek, U Suter, G J Snipes, A A Welcher, E M Shooter, R A Murphy. J Biol Chem 1993
103
15

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse.
U Suter, J J Moskow, A A Welcher, G J Snipes, B Kosaras, R L Sidman, A M Buchberg, E M Shooter. Proc Natl Acad Sci U S A 1992
268
15

Progesterone derivatives are able to influence peripheral myelin protein 22 and P0 gene expression: possible mechanisms of action.
R C Melcangi, V Magnaghi, I Cavarretta, I Zucchi, P Bovolin, D D'Urso, L Martini. J Neurosci Res 1999
101
15

Molecular dissection of the Schwann cell specific promoter of the PMP22 gene.
D Sabéran-Djoneidi, V Sanguedolce, Z Assouline, N Lévy, E Passage, M Fontés. Gene 2000
41
36


Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development.
D Baechner, T Liehr, H Hameister, H Altenberger, H Grehl, U Suter, B Rautenstrauss. J Neurosci Res 1995
90
15

Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease.
Edith Passage, Jean Chrétien Norreel, Pauline Noack-Fraissignes, Véronique Sanguedolce, Josette Pizant, Xavier Thirion, Andrée Robaglia-Schlupp, Jean François Pellissier, Michel Fontés. Nat Med 2004
237
14

The transcription factors SCIP and Krox-20 mark distinct stages and cell fates in Schwann cell differentiation.
T S Zorick, D E Syroid, E Arroyo, S S Scherer, G Lemke. Mol Cell Neurosci 1996
147
13

Genes specifically expressed at growth arrest of mammalian cells.
C Schneider, R M King, L Philipson. Cell 1988
821
13

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
S Bort, E Nelis, V Timmerman, T Sevilla, A Cruz-Martínez, F Martínez, J M Millán, J Arpa, J J Vílchez, F Prieto,[...]. Hum Genet 1997
119
13

Progesterone synthesis and myelin formation by Schwann cells.
H L Koenig, M Schumacher, B Ferzaz, A N Thi, A Ressouches, R Guennoun, I Jung-Testas, P Robel, Y Akwa, E E Baulieu. Science 1995
382
13


The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A.
L J Valentijn, P A Bolhuis, I Zorn, J E Hoogendijk, N van den Bosch, G W Hensels, V P Stanton, D E Housman, K H Fischbeck, D A Ross. Nat Genet 1992
315
12

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.
P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, J E Hoogendijk, F Baas, D F Barker, J J Martin, M De Visser, P A Bolhuis. Neuromuscul Disord 1991
426
12

Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic mice.
C Huxley, E Passage, A M Robertson, B Youl, S Huston, A Manson, D Sabéran-Djoniedi, D Figarella-Branger, J F Pellissier, P K Thomas,[...]. Hum Mol Genet 1998
126
12

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.
V Timmerman, E Nelis, W Van Hul, B W Nieuwenhuijsen, K L Chen, S Wang, K Ben Othman, B Cullen, R J Leach, C O Hanemann. Nat Genet 1992
381
12





Influence of elevated expression of rat wild-type PMP22 and its mutant PMP22Trembler on cell growth of NIH3T3 fibroblasts.
G Zoidl, D D'Urso, S Blass-Kampmann, C Schmalenbach, R Kuhn, H W Müller. Cell Tissue Res 1997
54
20

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.
N Matsunami, B Smith, L Ballard, M W Lensch, M Robertson, H Albertsen, C O Hanemann, H W Müller, T D Bird, R White. Nat Genet 1992
315
11


Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies.
L E Warner, P Mancias, I J Butler, C M McDonald, L Keppen, K G Koob, J R Lupski. Nat Genet 1998
366
11


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.