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Results:
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Results: 12
Targeted disruption of the Cln3 gene provides a mouse model for Batten disease (vol 6, pg 321, 1999)
Authors:
Mitchison, HM
Bernard, DJ
Greene, NDE
Cooper, JD
Junaid, MA
Pullarkat, RK
de Vos, N
Breuning, MH
Owens, JW
Mobley, WC
Gardiner, RM
Lake, BD
Taschner, PEM
Nussbaum, RL
Citation: Hm. Mitchison et al., Targeted disruption of the Cln3 gene provides a mouse model for Batten disease (vol 6, pg 321, 1999), NEUROBIOL D, 7(2), 2000, pp. 127-127
Authors:
Maiti, AK
Bartoloni, L
Mitchison, HM
Meeks, M
Chung, E
Spiden, S
Gehrig, C
Rossier, C
DeLozier-Blanchet, CD
Blouin, JL
Gardiner, RM
Antonarakis, SE
Citation: Ak. Maiti et al., No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD), CYTOG C GEN, 90(1-2), 2000, pp. 119-122
Authors:
Meeks, M
Walne, A
Spiden, S
Simpson, H
Mussaffi-Georgy, H
Hamam, HD
Fehaid, EL
Cheehab, M
Al-Dabbagh, M
Polak-Charcon, S
Blau, H
O'Rawe, A
Mitchison, HM
Gardiner, RM
Chung, E
Citation: M. Meeks et al., A locus for primary ciliary dyskinesia maps to chromosome 19q, J MED GENET, 37(4), 2000, pp. 241-244
Authors:
Greene, NDE
Bernard, DL
Taschner, PEM
Lake, BD
de Vos, N
Breuning, MH
Gardiner, RM
Mole, SE
Nussbaum, RL
Mitchison, HM
Citation: Nde. Greene et al., A murine model for juvenile NCL: Gene targeting of mouse CLn3 (vol 66, pg 309, 1999), MOL GEN MET, 67(4), 1999, pp. 368-368
Authors:
Stephenson, JBP
Greene, NDE
Leung, KY
Munroe, PB
Mole, SE
Gardiner, RM
Taschner, PEM
O'Regan, M
Naismith, K
Crow, YJ
Mitchison, HM
Citation: Jbp. Stephenson et al., The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in Scotland, MOL GEN MET, 66(4), 1999, pp. 245-247
Authors:
Greene, NDE
Bernard, DL
Taschner, PEM
Lake, BD
de Vos, N
Breuning, MH
Gardiner, RM
Mole, SE
Nussbaum, RL
Mitchison, HM
Citation: Nde. Greene et al., A murine model for juvenile NCL: Gene targeting of mouse Cln3, MOL GEN MET, 66(4), 1999, pp. 309-313
Authors:
Mole, SE
Mitchison, HM
Munroe, PB
Citation: Se. Mole et al., Molecular basis of the neuronal ceroid lipofuscinoses: Mutations in CLN1, CLN2, CLN3, and CLN5, HUM MUTAT, 14(3), 1999, pp. 199-215
Authors:
Mitchison, HM
Bernard, DJ
Greene, NDE
Cooper, JD
Junaid, MA
Pullarkat, RK
de Vos, N
Breuning, MH
Owens, JW
Mobley, WC
Gardiner, RM
Lake, BD
Taschner, PEM
Nussbaum, RL
Citation: Hm. Mitchison et al., Targeted disruption of the Cln3 gene provides a mouse model for Batten disease, NEUROBIOL D, 6(5), 1999, pp. 321-334
Authors:
Hofman, I
Kohlschutter, A
Santavuori, P
Gottlob, I
Goebel, HH
Lake, BD
Schutgens, RBH
Greene, NDE
Leung, KY
Mitchison, HM
Munroe, PB
Taschner, PEM
Citation: I. Hofman et al., Juvenile NCL, BIOM HLTH R, 33, 1999, pp. 55-76
Authors:
Lingaas, F
Mitchison, HM
Mole, SE
Koppang, N
Goebel, HH
Lake, BD
Citation: F. Lingaas et al., Animal models of NCL, BIOM HLTH R, 33, 1999, pp. 152-167
Authors:
Isosomppi, J
Heinonen, O
Hiltunen, JO
Greene, NDE
Vesa, J
Uusitalo, A
Mitchison, HM
Saarma, M
Jalanko, A
Peltonen, L
Citation: J. Isosomppi et al., Developmental expression of palmitoyl protein thioesterase in normal mice, DEV BRAIN R, 118(1-2), 1999, pp. 1-11
Authors:
Lauronen, L
Munroe, PB
Jarvela, I
Autti, T
Mitchison, HM
O'Rawe, AM
Gardiner, RM
Mole, SE
Puranen, J
Hakkinen, AM
Kirveskari, E
Santavuori, P
Citation: L. Lauronen et al., Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis, NEUROLOGY, 52(2), 1999, pp. 360-365
Risultati:
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