Chromosomal localization of the type-I 15-PGDH gene to 4q34–q35

被引：1
|
作者：
Franck Pichaud
Régis Delage-Mourroux
Elisabeth Pidoux
Annick Jullienne
Marie-Françoise Rousseau-Merck
机构：
[1] U.349 INSERM,
[2] Hopital Lariboisière,undefined
[3] Centre Viggo Petersen,undefined
[4] F-75475 Paris Cedex 10,undefined
[5] France,undefined
[6] U.301 INSERM,undefined
[7] Institut de Génétique Moléculaire,undefined
[8] 27 rue Juliette Dodu,undefined
[9] F-75010 Paris,undefined
[10] France Tel.: + 33 1 42499283; Fax: + 33 1 42069531,undefined
来源：
Human Genetics | 1997年 / 99卷
关键词：
Somatic Cell; Human Chromosome; Chromosomal Localization; Cell Hybrid; Somatic Cell Hybrid;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
The gene encoding the human NAD+-dependent 15-hydroxyprostaglandin dehydrogenase, designated type-I 15-PGDH, was mapped to chromosome 4 by analyzing its segregation in a panel of human-hamster somatic cell hybrids. This gene was further localized to bands 4q34–q35 by in situ hybridization on human chromosomes.
引用
收藏
页码：279 / 281
页数：2
相关论文
共 50 条
  • [1] Chromosomal localization of the type-I 15-PGDH gene to 4q34-q35
    Pichaud, F
    DelageMourroux, R
    Pidoux, E
    Jullienne, A
    RousseauMerck, MF
    HUMAN GENETICS, 1997, 99 (02) : 279 - 281
  • [2] GENE FOR WAARDENBURG SYNDROME TYPE-I IS LOCATED AT 2Q35, NOT AT 2Q37.3
    ISHIKIRIYAMA, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 46 (05): : 608 - 608
  • [3] A case report: prenatal diagnosis of 47,XX,der(15)t(4;15)(q35;q21.3)
    Guney, Taser
    Yesil, M.
    Sabuncuoglu, Y.
    Ozden, A.
    Umay, B.
    Yilanlioglu, N. C.
    Beyazyurek, C.
    Karadayi, H.
    Kahraman, S.
    Saglam, Y.
    CHROMOSOME RESEARCH, 2007, 15 : 111 - 112
  • [4] CHROMOSOMAL LOCALIZATION OF THE HUMAN GLYCOASPARAGINASE GENE TO 4Q32-Q33
    MORRIS, C
    HEISTERKAMP, N
    GROFFEN, J
    WILLIAMS, JC
    MONONEN, I
    HUMAN GENETICS, 1992, 88 (03) : 295 - 297
  • [5] Assignment of the ZYX gene for the LIM protein zyxin to human chromosome bands 7q34→q35 by in situ hybridization
    Zumbrunn, J
    Trueb, B
    CYTOGENETICS AND CELL GENETICS, 1998, 81 (3-4): : 283 - 284
  • [6] Localization of a gene for syndactyly type 1 to chromosome 2q34-q36
    Bosse, K
    Betz, RC
    Lee, YA
    Wienker, TF
    Reis, A
    Kleen, H
    Propping, P
    Cichon, S
    Nöthen, MM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) : 492 - 497
  • [7] WAARDENBURG SYNDROME TYPE-I IN A CHILD WITH DELETION-(2) (Q35Q36.2)
    KIRKPATRICK, SJ
    KENT, CM
    LAXOVA, R
    SEKHON, GS
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (05): : 699 - 700
  • [8] CHROMOSOMAL LOCALIZATION OF THE ARP-1 GENE TO 15Q26
    MODI, WS
    SEUANEZ, H
    MIETUSSNYDER, M
    OBRIEN, SJ
    KARATHANASIS, SK
    CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 1995 - 1995
  • [9] WAARDENBURG SYNDROME TYPE-I IN A CHILD WITH DENOVO INVERSION (2)(Q35Q37.3)
    ISHIKIRIYAMA, S
    TONOKI, H
    SHIBUYA, Y
    CHIN, S
    HARADA, N
    ABE, K
    NIIKAWA, N
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 33 (04): : 505 - 507
  • [10] PSEUDOHYPOPARATHYROIDISM TYPE-I AND ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH A PROXIMAL 15Q CHROMOSOMAL DELETION IN MOTHER AND DAUGHTER
    HEDELAND, H
    BERNTORP, K
    ARHEDEN, K
    KRISTOFFERSSON, U
    CLINICAL GENETICS, 1992, 42 (03) : 129 - 134
12345