THE 3:1 KIRKWOOD GAP AND THE MARIA FAMILY: GENETIC FAMILY MEMBERSHIP AND PROBABLE SOURCE BODY OF MESOSIDERITES

被引:0
|
作者
Fieber-Beyer, S. K. [1 ,5 ]
Gaffey, M. J. [1 ,2 ,5 ]
Kelley, M. S. [4 ,5 ]
Reddy, V. [1 ,2 ,5 ]
Reynolds, C. M. [1 ]
Hicks, T. [3 ]
机构
[1] Univ N Dakota, Dept Space Studies, Grand Forks, ND 58202 USA
[2] Univ N Dakota, Dept Earth Syst Sci & Policy, Grand Forks, ND 58202 USA
[3] Georgia So Univ, Dept Geol & Geog, Statesboro, GA 30460 USA
[4] Planetary Sci Div, Washington, DC USA
[5] Univ Hawaii, Hilo, HI 96720 USA
关键词
MOTION; RESONANCE; ASTEROIDS;
D O I
暂无
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
引用
收藏
页码:A54 / A54
页数:1
相关论文
共 18 条
  • [1] The Maria asteroid family: Genetic relationships and a plausible source of mesosiderites near the 3:1 Kirkwood Gap
    Fieber-Beyer, Sherry K.
    Gaffey, Michael J.
    Kelley, Michael S.
    Reddy, Vishnu
    Reynolds, Chalbeth M.
    Hicks, Tony
    ICARUS, 2011, 213 (02) : 524 - 537
  • [2] Near-infrared spectroscopy of 3:1 Kirkwood Gap asteroids II: Probable and plausible parent bodies; primitive and differentiated
    Fieber-Beyer, Sherry K.
    Gaffey, Michael J.
    ICARUS, 2014, 229 : 99 - 108
  • [3] Altered body as a source of interactional problems in the family of individuals with neurofibromatosis type 1-A polish study
    Kowal, Katarzyna
    Skrzypek, Michal
    PLOS ONE, 2024, 19 (11):
  • [4] Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome
    Kerkeni, Nesrine
    Kharrat, Maher
    Maazoul, Faouzi
    Boudabous, Hela
    M'rad, Ridha
    Trabelsi, Mediha
    JOURNAL OF CLINICAL NEUROLOGY, 2022, 18 (02): : 214 - 222
  • [5] ALPHA1-ANTITRYPSIN DEFICIENCY-GENETIC, CLINICAL AND FUNCTIONAL CORRELATIONS IN A 3 GENERATION FAMILY
    PERRAULT, JL
    MALO, JL
    BAKE, B
    RENZI, G
    GRASSINO, A
    RESPIRATION, 1979, 37 (05) : 291 - 300
  • [6] Pannexin 1 and pannexin 3 are glycoproteins that exhibit many distinct characteristics from the connexin family of gap junction proteins
    Penuela, Silvia
    Bhalla, Ruchi
    Gong, Xiang-Qun
    Cowan, Kyle N.
    Celetti, Steven J.
    Cowan, Bryce J.
    Bai, Donglin
    Shao, Qing
    Laird, Dale W.
    JOURNAL OF CELL SCIENCE, 2007, 120 (21) : 3772 - 3783
  • [7] IDENTIFICATION OF A SPECIFIC INS(1,3,4,5)P-4-BINDING PROTEIN AS A MEMBER OF THE GAP1 FAMILY
    CULLEN, PJ
    HSUAN, JJ
    TRUONG, O
    LETCHER, AJ
    JACKSON, TR
    DAWSON, AP
    IRVINE, RF
    NATURE, 1995, 376 (6540) : 527 - 530
  • [8] Genetic and biochemical characterization of Drosophila Snipper:: A promiscuous member of the metazoan 3′hExo/ERI-1 family of 3′ to 5′ exonucleases
    Kupsco, Jeremy M.
    Wu, Ming-Jing
    Marzluff, William F.
    Thapar, Roopa
    Duronio, Robert J.
    RNA, 2006, 12 (12) : 2103 - 2117
  • [9] Exome sequencing identifies a novel pathogenic variant in RAB3GAP1 causing Warburg Micro syndrome in a Pakistani family
    Ullah, Wahid
    Ilyas, Muhammad
    Tariq, Muhammad
    Imdad, Maria
    Ullah, Ikram
    Efthymiou, Stephanie
    Faheem, Muhammad
    Abbas, Muhammad
    Aamir, Muhammad
    Nouman, Muhammad
    Houlden, Henry
    SYNAPS Study Group, S. Y. N. A. P. S. Study Group
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2023, 83 (04) : 368 - 373
  • [10] LST-3TM12 IS A MEMBER OF THE OATP1B-FAMILY AND A FUNCTIONAL TRANSPORTER INFLUENCED BY GENETIC VARIANTS
    zu Schwabedissen, Henriette Meyer
    Malagnino, Vanessa
    Hussner, Janine
    Seibert, Isabell
    DRUG METABOLISM AND PHARMACOKINETICS, 2019, 34 (01) : S75 - S75