| 000 | 00000cam u2200205 a 4500 | |
| 001 | 000045990337 | |
| 005 | 20190711103820 | |
| 008 | 190710s2019 nyua b 001 0 eng d | |
| 020 | ▼a 9781493990795 | |
| 035 | ▼a (OCoLC)1059311951 | |
| 040 | ▼a YDX ▼b eng ▼e rda ▼c YDX ▼d BDX ▼d OCLCQ ▼d UKMGB ▼d HNK ▼d OCLCF ▼d KUB ▼d 211009 | |
| 050 | 4 | ▼a RJ506.F73 ▼b F73 2019 |
| 082 | 0 4 | ▼a 618.92/858841 ▼2 23 |
| 084 | ▼a 618.92858841 ▼2 DDCK | |
| 090 | ▼a 618.92858841 ▼b F811 | |
| 245 | 0 0 | ▼a Fragile-X syndrome : ▼b methods and protocols / ▼c edited by Dalit Ben-Yosef and Yoav Mayshar. |
| 260 | ▼a New York : ▼b Humana Press : ▼b Springer, ▼c 2019. | |
| 300 | ▼a x, 192 p. : ▼b ill. (some col.) ; ▼c 27 cm. | |
| 490 | 1 | ▼a Methods in molecular biology, ▼x 1940-6029 ; ▼v 1942 |
| 490 | 1 | ▼a Springer protocols |
| 504 | ▼a Includes bibliographical references and index. | |
| 650 | 0 | ▼a Fragile X syndrome ▼v Laboratory manuals. |
| 700 | 1 | ▼a Ben-Yosef, Dalit. |
| 700 | 1 | ▼a Mayshar, Yoav. |
| 830 | 0 | ▼a Methods in molecular biology ; ▼v 1942. |
| 830 | 0 | ▼a Springer protocols (Series). |
| 945 | ▼a KLPA |
소장정보
| No. | 소장처 | 청구기호 | 등록번호 | 도서상태 | 반납예정일 | 예약 | 서비스 |
|---|---|---|---|---|---|---|---|
| No. 1 | 소장처 과학도서관/Sci-Info(2층서고)/ | 청구기호 618.92858841 F811 | 등록번호 121249471 | 도서상태 대출가능 | 반납예정일 | 예약 | 서비스 |
컨텐츠정보
목차
Preface... Table of Contents... Contributing Authors... Part I FXS: Full Mutation An Introduction to FXS 1. Fragile-X Syndrome: Introduction Adi Reches Methods to Study FXS 2. Clinical Genetic Testing for Fragile-X Syndrome by Polymerase Chain Reaction Amplification and Southern Blot Analyses Xiaoqiang Cal, Mohammad Arif, Haolei Wan, Ruth Kornreich, and Lisa Edelmann 3. Monitoring for Epigenetic Modifications at the FMR1 Locus Silvina Epsztejn-Litman and Rachel Eiges 4. Assays for Determining Repeat Number, Methylation Status and AGG Interruptions in the Fragile X-Related Disorders Bruce E. Hayward and Karen Usdin 5. One-Step Generation of Seamless Luciferase Gene Knock-In Using CRISPR/Cas9 Genome Editing in Human Pluripotent Stem Cells Meng Li, Jack Hunt, Anita Bhattacharyya, and Xinyu Zhao 6. Modeling FXS with Mouse Neural Progenitors Ulla-Kaisa Peteri and Maija L. Castren 7. Using Human Neural Progenitor Cell Models to Conduct Large-Scale Drug Screens for Neurological and Psychiatric Diseases Jack Hunt, Meng Li, Xinyu Zhao, and Anita Bhattacharyya 8. Modeling FXS: Human Pluripotent Stem Cells and In Vitro Neural Differentiation Liron Kuznitsov-Yanovsky, Yoav Mayshar, and Dalit Ben-Yosef 9. Induced Neurons for the Study of Neurodegenerative and Neurodevelopmental Disorders Evelyn J. Sauter, Lisa K. Kutsche, Simon D. Klapper, and Volker Busskamp 10. Imaging of Somatic Ca2+ Transients in Differentiated Human Neurons Irena Vertkin and Dalit Ben-Yosef 11. Patch-Clamp Recordings from Human Embryonic Stem Cells-Derived Fragile X Neurons Michael Telias and Menahem Segal 12. Application of Drosophila Model towards Understanding the Molecular Basis of Fragile-X Syndrome Ha Eun Kong, Junghwa Lim, and Peng Jin Human vs Mouse in Fragile-X Syndrome Research 13. Comparing Mouse and Human-Based Models for Fragile-X Syndrome Pre-Clinical Research Michael Telias Part II FX Premutation Females FX Permutation: Primary Ovarian Insufficiency 14. Pathophysiology Mechanisms in Fragile-X Primary Ovarian Insufficiency Shai E. Elizur, Moran Friedman, Olga Dratviman-Storobinsky, and Yoram Cohen FX Permutation FXTAS 15. Fragile-X Associated Tremor/Ataxia Syndrome (FXTAS) Marwa Zafarullah and Flora Tassone
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