Association between obese Type 2 diabetes and the melanocortin 2 receptor gene (MC2R) on chromosome 18p11

被引:0
|
作者
Sjögren, M [1 ]
Svensson, M [1 ]
Fredriksson, J [1 ]
Groop, L [1 ]
Orho-Melander, M [1 ]
机构
[1] Inst Surg Med & Orthoped, Dept Endocrinol, Malmo, Sweden
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
361
引用
收藏
页码:A136 / A136
页数:1
相关论文
共 50 条
  • [21] Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder
    Washizuka, S
    Kakiuchi, C
    Mori, K
    Kunugi, H
    Tajima, O
    Akiyama, T
    Nanko, S
    Kato, T
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2003, 120B (01) : 72 - 78
  • [22] Loss of the C-Terminus of Melanocortin Receptor 2 (MC2R) Results in Impaired Cell Surface Expression and ACTH Insensitivity
    Hirsch, Andrea
    Audi, Laura
    Meimaridou, Eirini
    Clark, Adrian J. L.
    Fluck, Christa E.
    ENDOCRINE REVIEWS, 2010, 31 (03) : S2463 - S2463
  • [23] Trends in the evolution of the elasmobranch melanocortin-2 receptor: Insights from structure/function studies on the activation of whale shark Mc2r
    Hoglin, Brianne E.
    Miner, Marin V.
    Erbenebayar, Ugumuur
    Shaughnessy, Ciaran A.
    Dores, Robert M.
    GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2023, 338
  • [24] A Novel Mutation in the MC2R Gene Causing Familial Glucocorticoid Deficiency Type 1
    Akin, Mustafa Ali
    Akin, Leyla
    Coban, Dilek
    Ozturk, M. Adnan
    Bircan, Rifat
    Kurtoglu, Selim
    NEONATOLOGY, 2011, 100 (03) : 277 - 281
  • [25] C18orf2, a novel, highly conserved intronless gene within intron 5 of the GNAL gene on chromosome 18p11
    Vuoristo, JT
    Berrettini, WH
    Ala-Kokko, L
    CYTOGENETICS AND CELL GENETICS, 2001, 93 (1-2): : 19 - 22
  • [26] Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population
    Washizuka, S
    Kametani, M
    Sasaki, T
    Tochigi, M
    Umekage, T
    Kohda, K
    Kato, T
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (03) : 301 - 304
  • [27] A basal actinopterygian melanocortin receptor: Molecular and functional characterization of an Mc2r ortholog from the Senegal bichir (Polypterus senegalus)
    Shaughnessy, Ciaran A.
    Jensen, Mary F.
    Dores, Robert M.
    GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2022, 328
  • [28] A significant evidence for linkage of febrile seizures to chromosome 18p11 and possible association of a common haplotype in the IMPA2 gene in Japanese families.
    Nakayama, J
    Yamamoto, N
    Hamano, K
    Iwasaki, N
    Ohta, M
    Nakahara, S
    Matsui, A
    Noguchi, E
    Arinami, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 469 - 469
  • [29] Expression and role of the melanocortin 5 (MC5R) and MC2R receptors in the ovine fetal adrenal gland.
    Hyatt, K
    Myers, DA
    JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2006, 13 (02) : 73A - 73A
  • [30] Novel compound heterozygous mutation of the ACTH receptor gene (MC2R) in a familiar glucocorticoid deficiency
    Artigas, R.
    Carvajal, C.
    Cattani, A.
    Riquelme, E.
    Matinez, A.
    Kalergis, A.
    Fardella, C.
    HORMONE RESEARCH, 2007, 68 : 2 - 2