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GRUPO 31.
GENETICA MOLECULAR DE LAS DISTROGLICANOPATÍAS
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Publicaciones
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AÑO |
DENOMINACIÓN |
F.I. |
CUARTIL |
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2011 |
de Lucas-Cerrillo, A. M. ; Maldifassi, M. C.; Arnalich, F.; Renart, J.; Atienza, G.; Serantes, R.; Cruces, J.; Sánchez-Pacheco, A.; Andrés-Mateos, E.; Montiel, C. Function of Partially Duplicated Human alpha 7 Nicotinic Receptor Subunit CHRFAM7A gene potential implications for the cholinergic anti-inflammatory response. JOURNAL OF BIOLOGICAL CHEMISTRY. 2011; 286(1): 594-606. Article. |
4,773 |
Q1 |
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2010 |
Ruiz, J.; Martínez, A.; Hernández, S.; Zimman, H.; Ferrer, M.; Fernández, C.; Sáez, M.; López-Asenjo, J. A.; Sanz-Ortega, J. Clinicopathological variables, immunophenotype, chromosome 1p36 loss and tumour recurrence of 247 meningiomas grade I and II. HISTOLOGY AND HISTOPATHOLOGY. 2010; 25(3): 341-349. Article. |
2,502 |
Q2
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2010 |
Lommel, M.; Willer, T.; Cruces, J.; Strahl, S. Pomt1 is essential for protein o-mannosylation in mammals. METHODS IN ENZYMOLOGY. 2010; 479: 323-342. Review. |
1,626 |
Q3
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2009 |
Cotarelo, RP; Fano, O; Raducu, M; Pena, A; Tarilonte, P; Mateos, F; Simon, R; Cabello, A; Cruces, J. A double homozygous mutation in the POMT1 gene involving exon skipping gives rise to Walker-Warburg syndrome in two Spanish Gypsy families. CLINICAL GENETICS. 2009; 76(1): 108-112 |
3,304 |
Q2
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