Genetic mapping of Chuvash Polycythemia: An autosomal recessive disorder of oxygen sensing.

被引：0
|
作者：
Stockton, DW
Chen, H
Ang, SO
Sergeyeva, AI
Gordeuk, VR
Polyakova, LA
Prchal, JT
机构：
[1] Baylor Coll Med, Houston, TX 77030 USA
[2] Chuvash State Univ, Cheboksary, Russia
[3] Howard Univ, Washington, DC 20059 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2001年 / 69卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2507
引用
收藏
页码：608 / 608
页数：1
相关论文
共 44 条
  • [1] Chuvash polycythemia: An autosomal recessive disorder of dysregulated oxygen sensing.
    Ang, SO
    Kralovics, R
    Adelina, S
    Gordeuk, VR
    Prchal, JT
    BLOOD, 2000, 96 (11) : 5A - 5A
  • [2] Von Hippel-Lindau protein, Chuvash polycythemia, and oxygen sensing.
    Ang, SO
    Chen, H
    Stockton, DW
    Sergueeva, A
    Gordeuk, VR
    Prchal, JT
    BLOOD, 2001, 98 (11) : 748A - 748A
  • [3] Oxygen sensing and Chuvash Polycythemia
    Ang, S
    Stockton, D
    Hirota, K
    Gordeuk, V
    Jelinek, J
    Sergueeva, A
    Maxwell, P
    Semenza, G
    Prchal, J
    EXPERIMENTAL HEMATOLOGY, 2002, 30 (06) : 43 - 43
  • [4] Congenital disorder of oxygen sensing:: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors
    Gordeuk, VR
    Sergueeva, AI
    Miasnikova, GY
    Okhotin, D
    Voloshin, Y
    Choyke, PL
    Butman, JA
    Jedlickova, K
    Prchal, JT
    Polyakova, LA
    BLOOD, 2004, 103 (10) : 3924 - 3932
  • [5] Putative dysregulation in the HIF-1 oxygen sensing pathway in congenital chuvash polycythemia.
    Ang, SO
    Buchanan, GR
    Gordeuk, VR
    Prchal, JT
    BLOOD, 1999, 94 (10) : 412A - 412A
  • [6] Genetic mapping of autosomal recessive retinitis pigmentosa in the Sardinian population
    Wright, AF
    Bruford, EA
    Manson, FDC
    Fossarello, M
    Porter, K
    Scott, K
    Richards, JE
    Farber, DB
    Swaroop, A
    Mansfield, DC
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1997, 38 (04) : 5337 - 5337
  • [7] GENETIC AND PHYSICAL MAPPING OF AUTOSOMAL RECESSIVE SPINAL MUSCULAR-ATROPHY (SMA)
    MORRISON, KE
    DANIELS, RJ
    FRANCIS, MJ
    CAMPBELL, L
    CHRISTODOULOU, Z
    NESBIT, A
    THEODOSIOU, A
    PATEL, S
    DUBOWITZ, V
    WASMUTH, JJ
    MACPHERSON, J
    IGNATIUS, J
    DAVIES, KE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 132 - 132
  • [8] NEUTROPHIL (PMN) ACTIN DYSFUNCTION - AN AUTOSOMAL RECESSIVE GENETIC DISORDER OF ACTIN MOLECULES
    SOUTHWICK, FS
    STOSSEL, TP
    CLINICAL RESEARCH, 1981, 29 (02): : A397 - A397
  • [9] STRATEGIES AND SAMPLE-SIZE CONSIDERATIONS FOR MAPPING A 2-LOCUS AUTOSOMAL RECESSIVE DISORDER
    MAJUMDER, PP
    AMERICAN JOURNAL OF HUMAN GENETICS, 1989, 45 (03) : 412 - 423
  • [10] Genetic mapping and identification of a new autosomal nonsyndromic recessive deafness locus DFNB37.
    Ahmed, ZM
    Morell, RJ
    Riazuddin, S
    Ahmad, MM
    Mohiddin, SA
    Caruso, RC
    Khan, SN
    Fananapazir, L
    Husnain, T
    Griffith, AJ
    Riazuddin, S
    Friedman, TB
    Wilcox, ER
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 528 - 528
12345