Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism

被引:0
|
作者
Johanna Känsäkoski
Rainer Fagerholm
Eeva-Maria Laitinen
Kirsi Vaaralahti
Peter Hackman
Nelly Pitteloud
Taneli Raivio
Johanna Tommiska
机构
[1] Institute of Biomedicine/Physiology,Department of Obstetrics and Gynecology
[2] University of Helsinki,Department of Medical Genetics
[3] Children’s Hospital,undefined
[4] Helsinki University Central Hospital,undefined
[5] Helsinki University Central Hospital,undefined
[6] Folkhälsan Institute of Genetics,undefined
[7] Haartman Institute,undefined
[8] University of Helsinki,undefined
[9] Service of Endocrinology,undefined
[10] Diabetes and Metabolism,undefined
[11] Centre Hospitalier Universitaire Vaudois,undefined
[12] University of Lausanne,undefined
来源
Pediatric Research | 2014年 / 75卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:641 / 644
页数:3
相关论文
共 50 条
  • [21] Rod Photoreceptor neuritic sprouting is responsive to Sema3A
    Kung, Frank
    Axelrod, Abram
    Siegel, Dionicio
    Townes-Anderson, Ellen
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (15)
  • [22] Pan-Cancer Analysis of the Prognostic and Immunological Role of SEMA7A
    Yang, Lixian
    Zhang, Shiyu
    Zheng, Lei
    Kong, Fanting
    Dang, Wei
    Shen, Shipeng
    Li, Xiaowei
    Jia, Lining
    Zhang, Xiaoru
    Lu, Na
    INTERNATIONAL JOURNAL OF GENERAL MEDICINE, 2024, 17 : 6443 - 6461
  • [23] Intracellular signaling of Sema3A through phosphorylation cascade
    Nakamura, Fumio
    Goshima, Yoshio
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2016, 130 (03) : S35 - S35
  • [24] The CRMP family of proteins and their role in Sema3A signaling
    Schmidt, Eric F.
    Strittmatter, Stephen M.
    SEMIAPHORINS: RECEPTOR AND INTRACELLULAR SIGNALING MECHANISMS, 2007, 600 : 1 - 11
  • [25] Identification of SEMA4D as a novel causal gene of idiopathic hypogonadotropic hypogonadism
    Wang, D.
    Niu, Y.
    Xu, H.
    Liu, J.
    EUROPEAN UROLOGY, 2022, 81 : S604 - S604
  • [26] SEMA3A蛋白功能研究进展
    戴文婷
    蒋最明
    顾敏
    国际遗传学杂志, 2020, 43 (06) : 349 - 352
  • [27] Sema3A and NGF interplay in regeneration of DRG axons
    Kaselis, Andrius
    Treinys, Rimantas
    Vosyliute, Ruta
    Satkauskas, Saulius
    ACTA PHYSIOLOGICA, 2015, 215 : 112 - 112
  • [28] SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
    Hanchate, Naresh Kumar
    Giacobini, Paolo
    Lhuillier, Pierre
    Parkash, Jyoti
    Espy, Cecile
    Fouveaut, Corinne
    Leroy, Chrystel
    Baron, Stephanie
    Campagne, Celine
    Vanacker, Charlotte
    Collier, Francis
    Cruaud, Corinne
    Meyer, Vincent
    Garcia-Pinero, Alfons
    Dewailly, Didier
    Cortet-Rudelli, Christine
    Gersak, Ksenija
    Metz, Chantal
    Chabrier, Gerard
    Pugeat, Michel
    Young, Jacques
    Hardelin, Jean-Pierre
    Prevot, Vincent
    Dode, Catherine
    PLOS GENETICS, 2012, 8 (08):
  • [29] Dysfunctional SEMA3G signalling underlies familiar hypogonadotropic hypogonadism & defective GnRH neuron migration
    Cariboni, A.
    Lettieri, A.
    Oleari, R.
    Tahir, S.
    Hussain, K.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 826 - 826
  • [30] PTEN couples Sema3A signalling to growth cone collapse
    Chadborn, NH
    Ahmed, AI
    Holt, MR
    Prinjha, R
    Dunn, GA
    Jones, GE
    Eickholt, BJ
    JOURNAL OF CELL SCIENCE, 2006, 119 (05) : 951 - 957