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Results:
1-10
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Results: 10
Authors:
Flugel, A
Berkowicz, T
Ritter, T
Labeur, M
Jenne, DE
Li, ZX
Ellwart, JW
Willem, M
Lassmann, H
Wekerle, H
Citation: A. Flugel et al., Migratory activity and functional changes of green fluorescent effector cells before and during experimental autoimmune encephalomyelitis, IMMUNITY, 14(5), 2001, pp. 547-560
Authors:
Jenne, DE
Tinschert, S
Reimann, H
Lasinger, W
Thiel, G
Hameister, H
Kehrer-Sawatzki, H
Citation: De. Jenne et al., Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions, AM J HU GEN, 69(3), 2001, pp. 516-527
Authors:
Puttagunta, R
Gordon, LA
Meyer, GE
Kapfhamer, D
Lamerdin, JE
Kantheti, P
Portman, KM
Chung, WK
Jenne, DE
Olsen, AS
Burmeister, M
Citation: R. Puttagunta et al., Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints, GENOME RES, 10(9), 2000, pp. 1369-1380
Authors:
Moreira, ES
Wiltshire, TJ
Faulkner, G
Nilforoushan, A
Vainzof, M
Suzuki, OT
Valle, G
Reeves, R
Zatz, M
Passos-Bueno, MR
Jenne, DE
Citation: Es. Moreira et al., Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin, NAT GENET, 24(2), 2000, pp. 163-166
Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene
Authors:
Tinschert, S
Naumann, I
Stegmann, E
Buske, A
Kaufmann, D
Thiel, G
Jenne, DE
Citation: S. Tinschert et al., Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene, EUR J HUM G, 8(6), 2000, pp. 455-459
Authors:
Jenne, DE
Tinschert, S
Stegmann, E
Reimann, H
Nurnberg, P
Horn, D
Naumann, I
Buske, A
Thiel, G
Citation: De. Jenne et al., A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions, GENOMICS, 66(1), 2000, pp. 93-97
Authors:
Friedl, W
Kruse, R
Uhlhaas, S
Stolte, M
Schartmann, B
Keller, KM
Jungck, M
Stern, M
Loff, S
Back, W
Propping, P
Jenne, DE
Citation: W. Friedl et al., Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients, GENE CHROM, 25(4), 1999, pp. 403-406
Authors:
Wilharm, E
Parry, MAA
Friebel, R
Tschesche, H
Matschiner, G
Sommerhoff, CP
Jenne, DE
Citation: E. Wilharm et al., Generation of catalytically active granzyme K from Escherichia coli inclusion bodies and identification of efficient granzyme K inhibitors in human plasma, J BIOL CHEM, 274(38), 1999, pp. 27331-27337
Authors:
Wilharm, E
Tschopp, J
Jenne, DE
Citation: E. Wilharm et al., Biological activities of granzyme K are conserved in the mouse and accountfor residual Z-Lys-SBzl activity in granzyme A-deficient mice, FEBS LETTER, 459(1), 1999, pp. 139-142
Authors:
Wong, ETL
Jenne, DE
Zimmer, M
Porter, SD
Gilks, CB
Citation: Etl. Wong et al., Changes in chromatin organization at the neutrophil elastase locus associated with myeloid cell differentiation, BLOOD, 94(11), 1999, pp. 3730-3736
Risultati:
1-10
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