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TITLE: An Intriguing Shift Occurs in the Novel Protein Phosphatase 1 Binding Partner, TCTEX1D4: Evidence of Positive Selection in a Pika Model  Full Text
AUTHORS: Korrodi Gregorio, L ; Lopes, AM; Esteves, SLC; Afonso, S; de Matos, AL; Lissovsky, AA; Silva, OABDE; Silva, EFDE; Esteves, PJ ; Fardilha, M ;
PUBLISHED: 2013, SOURCE: PLOS ONE, VOLUME: 8, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 4
23
TITLE: Population Genomics/Macro vs Microevolution
AUTHORS: Alves, JM; Lopes, AM;
PUBLISHED: 2013, SOURCE: Brenner's Encyclopedia of Genetics: Second Edition
INDEXED IN: Scopus
25
TITLE: Methylation of twoHomo sapiens-specific X-Y homologous genes in Klinefelter's syndrome (XXY)  Full Text
AUTHORS: Norman L.J Ross; Rekha Wadekar; Alexandra Lopes; Adam Dagnall; James Close; Lynn E DeLisi; Timothy J Crow;
PUBLISHED: 2006, SOURCE: Am. J. Med. Genet. - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, VOLUME: 141B, ISSUE: 5
INDEXED IN: CrossRef: 22
IN MY: ORCID
26
TITLE: Microsatellite variation and evolution of human lactase persistence  Full Text
AUTHORS: Coelho, M; Luiselli, D; Bertorelle, G; Lopes, AI; Seixas, S ; Destro Bisol, G; Rocha, J ;
PUBLISHED: 2005, SOURCE: HUMAN GENETICS, VOLUME: 117, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 90
27
TITLE: Quantitating progression in ALS
AUTHORS: de Carvalho, M; Scotto, M ; Lopes, A; Swash, M ;
PUBLISHED: 2005, SOURCE: NEUROLOGY, VOLUME: 64, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 47
28
TITLE: Clinical and neurophysiological evaluation of progression in amyotrophic lateral sclerosis  Full Text
AUTHORS: de Carvalho, M; Scotto, M ; Lopes, A; Swash, M ;
PUBLISHED: 2003, SOURCE: MUSCLE & NERVE, VOLUME: 28, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 31
29
TITLE: F-waves and the corticospinal lesion in amyotrophic lateral sclerosis  Full Text
AUTHORS: de Carvalho, M; Scotto, M ; Lopes, A; Swash, M ;
PUBLISHED: 2002, SOURCE: AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, VOLUME: 3, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 24
30
TITLE: Association between the defective Pro369Ser mutation and in vivo intrahepatic alpha 1-antitrypsin accumulation
AUTHORS: Seixas, S ; Lopes, AI; Rocha, J ; Silva, L; Salgueiro, C; Salazar de Sousa, J; Batista, A;
PUBLISHED: 2001, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 38, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 3
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