Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

The multiple endocrine neoplasia type 1 (MEN1) locus has been previously localised to 11q13 by combined tumour deletion mapping and recombination studies, and a 0.5-Mb region, flanked by PYGM and D11S449, has been defined. In the course of constructing a conting, we have identified the location of t...

Mô tả đầy đủ

Chi tiết về thư mục
Những tác giả chính:	Forbes, SA, Pannett, A, Bassett, J, Harding, B, Wooding, C, Thakker, R, Butler, R, Ogilvie, D, Anand, R, Gaudray, P, Weber, G, Larsson, C, Zhang, C, Calender, A, Höppener, J, Lips, C, Kas, K
Định dạng:	Journal article
Ngôn ngữ:	English
Được phát hành:	1997

Những quyển sách tương tự

The European Consortium on MEN1. Mapping of the gene encoding the B56β subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)
Bằng: Forbes, SA, et al.
Được phát hành: (1997)

Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13
Bằng: Courseaux, A, et al.
Được phát hành: (1996)

Definition of the Minimal MEN1 Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13
Bằng: Courseaux, A, et al.
Được phát hành: (1996)

Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Neoplasies Endocriniennes Multiples de type 1).
Bằng: Courseaux, A, et al.
Được phát hành: (1996)

A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1.
Bằng: Höppener, J, et al.
Được phát hành: (1998)

The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)
Bằng: Bassett, J, et al.
Được phát hành: (1997)

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.
Bằng: Lemmens, I, et al.
Được phát hành: (1997)

The European Consortium on MEN1. Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1).
Bằng: Bassett, J, et al.
Được phát hành: (1997)

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.
Bằng: Trump, D, et al.
Được phát hành: (1998)

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.
Bằng: Bassett, J, et al.
Được phát hành: (1999)

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene
Bằng: Lemmens, I, et al.
Được phát hành: (1997)

[1,4]Ditellurino[2,3-b:5,6-b′]dipyrazine
Bằng: Donna Franklin, et al.
Được phát hành: (2022-06-01)

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.
Bằng: Lemmens, I, et al.
Được phát hành: (1997)

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.
Bằng: Williamson, C, et al.
Được phát hành: (1997)

Meta-analysis of 31 studies reporting 344 mutations in the multiple endocrine neoplasia type 1 (MEN1) gene.
Bằng: Pannett, A, et al.
Được phát hành: (1999)

Expression and distribution of <it>PPP2R5C </it>gene in leukemia
Bằng: Li Bo, et al.
Được phát hành: (2011-05-01)

The coenzyme B12 precursor 5,6-dimethylbenzimidazole is a flavin antagonist in Salmonella
Bằng: Lahiru Malalasekara, et al.
Được phát hành: (2023-08-01)

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
Bằng: Lemmens, I, et al.
Được phát hành: (1997)

LOCALIZATION OF THE GENE CAUSING X-LINKED RECESSIVE NEPHROLITHIASIS TO THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
Bằng: Scheinman, S, et al.
Được phát hành: (1992)

A Nonsynonymous/Synonymous Substitution Analysis of the B56 Gene Family Aids in Understanding B56 Isoform Diversity.
Bằng: Osama Qureshi, et al.
Được phát hành: (2015-01-01)

X-linked hypophosphataemic rickets in a Saudi Arabian kindred results from a nonsense mutation of the PEX gene.
Bằng: Dixon, P, et al.
Được phát hành: (1997)

用于34Mb/s光纤传输系统的5B6B线路码
Bằng: 林凤紫
Được phát hành: (1987-01-01)

Somatic Mutations of the PPP2R1B Candidate Tumor Suppressor Gene at Chromosome 11q23 are Infrequent in Ovarian Carcinomas
Bằng: Rong Wu, et al.
Được phát hành: (1999-10-01)

Supplementing lactating dairy cows with a vitamin B12 precursor, 5,6-dimethylbenzimidazole, increases the apparent ruminal synthesis of vitamin B12
Bằng: A. Brito, et al.
Được phát hành: (2015-01-01)

Expression and chromosomal localization of the Requiem gene.
Bằng: Gabig, T, et al.
Được phát hành: (1998)

PPP/INS Tight Integration with BDS−3 PPP−B2b Service in the Urban Environment
Bằng: Luguang Lai, et al.
Được phát hành: (2023-02-01)

Evaluation of PPP2R5C gene expression in Iranian patients with B-Acute lymphoblastic leukemia and its association with clinical and laboratory findings
Bằng: Esmaeil Rostami, et al.
Được phát hành: (2017-09-01)

HADRON SPECTRUM IN QCD AT 6/G2=5.6
Bằng: Bitar, K, et al.
Được phát hành: (1990)

MAPPING OF THE X-LINKED IDIOPATHIC HYPOPARATHYROID GENE TO XQ26-XQ27 BY LINKAGE STUDIES
Bằng: Thakker, R, et al.
Được phát hành: (1989)

ISOLATION AND CHARACTERIZATION OF GENES-CODING FOR CYTOCHROME-B5 AND CYTOCHROME-B5 REDUCTASE
Bằng: Rigby, J, et al.
Được phát hành: (1989)

Initial Assessment of BDS PPP-B2b Service: Precision of Orbit and Clock Corrections, and PPP Performance
Bằng: Zhixi Nie, et al.
Được phát hành: (2021-05-01)

LOCALIZATION OF A TUMOR-SUPPRESSOR GENE CAUSING PARATHYROID TUMORS TO CHROMOSOME-1P34-P36
Bằng: Williamson, C, et al.
Được phát hành: (1995)

Identification of STAT5A and STAT5B target genes in human T cells.
Bằng: Takahiro Kanai, et al.
Được phát hành: (2014-01-01)

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
Bằng: Scheinman, S, et al.
Được phát hành: (1993)

Karabinek reprezentacyjny MSBS-5,56R systemu MSBS-5,56
Bằng: Ryszard WOŹNIAK, et al.
Được phát hành: (2018-09-01)

A 5-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a 6-generation Arkansas kindred.
Bằng: Mumm, S, et al.
Được phát hành: (2000)

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.
Bằng: Thakker, R, et al.
Được phát hành: (1990)

Characterization of mutations in patients with multiple endocrine neoplasia type 1.
Bằng: Bassett, J, et al.
Được phát hành: (1998)

trans-5,6-Diphenylperhydropyran-2,4-dione
Bằng: Valéria R. S. Malta, et al.
Được phát hành: (2009-02-01)

Seven novel mutations in the PEX gene indicate molecular heterogeneity for X-linked hypophosphataemic rickets.
Bằng: Dixon, P, et al.
Được phát hành: (1996)