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André Rosenthal

Veröffentlichungen von André Rosenthal zu Rosenthal, André ->
weitere Veröffentlichungen von André Rosenthal:
Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X–linked hydrocephalus (1992)
The Structure and Gene Repertoire of an Ancient Red Algal Plastid Genome (2000)
Expression analysis using low amounts of mRNA and GeneChips (1999)
A missense mutation confirms the L1 defect in X–linked hydrocephalus (HSAS) (1993)
Molecular basis of symbiosis between Rhizobium and legumes (1997)
Comparative analysis of the PCOLCE region in Fugu rubripes using a new automated annotation tool (2000)
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions (2000)
X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene (1994)
A genome-wide survey of RAS transformation targets (2000)
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome (1997)
An L-type calcium-channel gene mutated in incomplete X-linked congenitalstationary night blindness (1998)
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangealsyndrome type I (2000)
Positional cloning of the gene for X-linked retinitis pigmentosa 2 (1998)
Inactivating mutations and overexpression of BCL10, a caspaserecruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32) (1999)
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 (2003)
Veröffentlichungen zu Rosenthal, André
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1
Rosenthal, André, Jouet, Monique, ... Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X–linked hydrocephalus
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 2, No. 2 (1992), p. 107-112
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1992
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2
Glöckner, Gernot, Rosenthal, André, ... The Structure and Gene Repertoire of an Ancient Red Algal Plastid Genome
in: Journal of molecular evolution , ISSN 1432-1432, Vol. 51 (4. 2000), p. 382-390
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2000
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3
Pilarsky, Christian, Schmitt, Armin, ... Expression analysis using low amounts of mRNA and GeneChips
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 23 Suppl 1, No. 3s (1999), p. 68-68
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1999
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4
Jouet, Monique, Rosenthal, André, ... A missense mutation confirms the L1 defect in X–linked hydrocephalus (HSAS)
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 4, No. 4 (1993), p. 331-331
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1993
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5
Freiberg, Christoph, Fellay, Rémy, ... Molecular basis of symbiosis between Rhizobium and legumes
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 387, No. 6631 (1997), p. 394-401
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1997
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6
Tunnicliffe, Giorgia Romina Riboldi, Gloeckner, Gernot, ... Comparative analysis of the PCOLCE region in Fugu rubripes using a new automated annotation tool
in: Mammalian genome , ISSN 1432-1777, Vol. 11 (3. 2000), p. 213-219
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2000
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7
Reichwald, Kathrin, Thiesen, Jens, ... Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions
in: Mammalian genome , ISSN 1432-1777, Vol. 11 (3. 2000), p. 182-190
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2000
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8
Jouet, Monique, Rosenthal, André, ... X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 7, No. 3 (1994), p. 402-407
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1994
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9
Zuber, Johannes, Tchernitsa, Oleg I., ... A genome-wide survey of RAS transformation targets
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 24, No. 2 (2000), p. 144-152
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2000
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10
Rao, Ercole, Weiss, Birgit, ... Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 16, No. 1 (1997), p. 54-63
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1997
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11
Strom, Tim M., Nyakatura, Gerald, ... An L-type calcium-channel gene mutated in incomplete X-linked congenitalstationary night blindness
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 3 (1998), p. 260-263
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1998
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12
Momeni, Parastoo, Glöckner, Gernot, ... Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangealsyndrome type I
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 24, No. 1 (2000), p. 71-74
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2000
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13
Schwahn, Uwe, Lenzner, Steffen, ... Positional cloning of the gene for X-linked retinitis pigmentosa 2
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 4 (1998), p. 327-332
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1998
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14
Zhang, Quangeng, Siebert, Reiner, ... Inactivating mutations and overexpression of BCL10, a caspaserecruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32)
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 22, No. 1 (1999), p. 63-68
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1999
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15
Mburu, Philomena, Mustapha, Mirna, ... Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 34, No. 4 (2003), p. 421-428
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2003
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16
Glöckner, Gernot, Eichinger, Ludwig, ... Sequence and analysis of chromosome 2 of Dictyostelium discoideum
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 418, No. 6893 (2002), p. 79-85
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2002
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17
Nusbaum, Chad, Mikkelsen, Tarjei S., ... DNA sequence and analysis of human chromosome 8
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 439, No. 7074 (2006), p. 331-335
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2006
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18
McPherson, John D., Marra, Marco, ... A physical map of the human genome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 409, No. 6822 (2001), p. 934-941
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2001
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19
Lander, Eric S., Linton, Lauren M., ... Initial sequencing and analysis of the human genome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 409, No. 6822 (2001), p. 860-921
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2001
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20
Ross, Mark T., Grafham, Darren V., ... The DNA sequence of the human X chromosome
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 434, No. 7031 (2005), p. 325-337
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2005