Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
Shinsei Minoshima

Veröffentlichungen von Shinsei Minoshima zu Minoshima, Shinsei ->
weitere Veröffentlichungen von Shinsei Minoshima:
Precise mapping of the EGF receptor gene on the human chromosome 7p12 using an improved fish technique (1993)
Cot-1 banding of human chromosomes using fluorescencein situ hybridization with Cy3 labeling (1995)
Methylation status of ribosomal RNA gene clusters in the flow-sorted human acrocentric chromosomes (1992)
Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene (2000)
Assignment of the myeloperoxidase geneMPO to human chromosome 17 using somatic cell hybrids and flow-sorted chromosomes (1988)
Localization of human phosphoribosylpyrophosphate synthetase subunit I and II genes (PRPS1 and PRPS2) to different regions of the X chromosome and assignment of two PRPS1-related genes to autosomes (1989)
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism (1998)
Novel nuclear localization signal between the two DNA-binding zinc fingers in the human vitamin D receptorJ.-C.H. and Y.S. contributed equally to this work. (1998)
Single–minded and Down syndrome? (1995)
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase (2000)
Human glial fibrillary acidic protein (GFAP): molecular cloning of the complete cDNA sequence and chromosomal localization (chromosome 17) of the GFAP gene (1992)
Positional cloning of the APECED gene (1997)
Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequence (1998)
Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome (1998)
Insertion of β-satellite repeats identifies a transmembrane proteasecausing both congenital and childhood onset autosomal recessive deafness (2001)
Veröffentlichungen zu Minoshima, Shinsei
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Wang, Yimin, Minoshima, Shinsei, ... Precise mapping of the EGF receptor gene on the human chromosome 7p12 using an improved fish technique
in: Journal of human genetics , ISSN 1435-232X, Vol. 38 (4. 1993), p. 399-406
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
2
Wang, Yimin, Minoshima, Shinsei, ... Cot-1 banding of human chromosomes using fluorescencein situ hybridization with Cy3 labeling
in: Journal of human genetics , ISSN 1435-232X, Vol. 40 (3. 1995), p. 243-252
Zugang: zum Volltext
ähnliche Vorschläge
1995
zeige Details
3
Kawasaki, Kazuhiko, Minoshima, Shinsei, ... Methylation status of ribosomal RNA gene clusters in the flow-sorted human acrocentric chromosomes
in: Mammalian genome , ISSN 1432-1777, Vol. 3 (3. 1992), p. 173-178
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
4
Kitada, Tohru, Asakawa, Shuichi, ... Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene
in: Mammalian genome , ISSN 1432-1777, Vol. 11 (6. 2000), p. 417-421
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
5
Kudoh, Jun, Minoshima, Shinsei, ... Assignment of the myeloperoxidase geneMPO to human chromosome 17 using somatic cell hybrids and flow-sorted chromosomes
in: Journal of human genetics , ISSN 1435-232X, Vol. 33 (3. 1988), p. 315-324
Zugang: zum Volltext
ähnliche Vorschläge
1988
zeige Details
6
Taira, Masanori, Kudoh, Jun, ... Localization of human phosphoribosylpyrophosphate synthetase subunit I and II genes (PRPS1 and PRPS2) to different regions of the X chromosome and assignment of two...
in: Somatic cell and molecular genetics , ISSN 1572-9931, Vol. 15 (1. 1989), p. 29-37
Zugang: zum Volltext
ähnliche Vorschläge
1989
zeige Details
7
Kitada, Tohru, Asakawa, Shuichi, ... Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 392, No. 6676 (1998), p. 605-608
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
8
Hsieh, Jui-Cheng., Shimizu, Yoshiko., ... Novel nuclear localization signal between the two DNA-binding zinc fingers in the human vitamin D receptorJ.-C.H. and Y.S. contributed equally to this work.
in: Journal of Cellular Biochemistry, in: Journal of Cellular Biochemistry . - New York, N.Y. : Alan R. Liss, Inc, ISSN 0730-2312, ZDB-ID 1479976-5 Vol. 70 (1. 1998), p. 94-109
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
9
Chen, Haiming, Chrast, Roman, ... Single–minded and Down syndrome?
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 10, No. 1 (1995), p. 9-10
Zugang: zum Volltext
ähnliche Vorschläge
1995
zeige Details
10
Shimura, Hideki, Hattori, Nobutaka, ... Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 25, No. 3 (2000), p. 302-305
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
11
Kumanishi, Toshiro, Usui, Hiroshi, ... Human glial fibrillary acidic protein (GFAP): molecular cloning of the complete cDNA sequence and chromosomal localization (chromosome 17) of the GFAP gene
in: Acta neuropathologica , ISSN 1432-0533, Vol. 83 (6. 1992), p. 569-578
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
12
Nagamine, Kentaro, Peterson, Pärt, ... Positional cloning of the APECED gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 17, No. 4 (1997), p. 393-398
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
13
Guipponi, Michel, Scott, Hamish S., ... Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure...
in: Human genetics , ISSN 1432-1203, Vol. 103 (4. 1998), p. 386-392
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
14
Matsuoka, R., Kimura, Misa, ... Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome
in: Human genetics , ISSN 1432-1203, Vol. 103 (1. 1998), p. 70-80
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
15
Scott, Hamish S., Kudoh, Jun, ... Insertion of β-satellite repeats identifies a transmembrane proteasecausing both congenital and childhood onset autosomal recessive deafness
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 27, No. 1 (2001), p. 59-63
Zugang: zum Volltext
ähnliche Vorschläge
2001
zeige Details
16
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
Zugang: zum Volltext
ähnliche Vorschläge
2006
zeige Details
17
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
Zugang: zum Volltext
ähnliche Vorschläge
2001
zeige Details
18
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
Zugang: zum Volltext
ähnliche Vorschläge
2001