Ayala Lagziel : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (15)
Les plus populaires
Liste
- Liste
- Tableau

1

XDH gene mutation is the underlying cause of classical xanthinuria: A second report

Levartovsky, David, Lagziel, Ayala, Sperling, Oded, Liberman, Uri, Yaron, Michael, Hosoya, Tatsuo, Ichida, Kimiyoshi, Peretz, Hava

Journal:

Kidney International

Année:

2000

Langue:

english

Fichier:

PDF, 273 KB

english, 2000

2

Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins

Liron Elkouby-Naor, Zaid Abassi, Ayala Lagziel, Alexander Gow, Tamar Ben-Yosef

Journal:

Cell and Tissue Research

Année:

2008

Langue:

english

Fichier:

PDF, 517 KB

english, 2008

3

Warfarin therapy is feasible in CYP2C9*3 homozygous patients

Jacob Ablin, Shaltiel Cabili, Amiram Eldor, Ayala Lagziel, Hava Peretz

Journal:

European Journal of Internal Medicine

Année:

2004

Langue:

english

Fichier:

PDF, 162 KB

english, 2004

4

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

Ayala Lagziel, Zubair M. Ahmed, Julie M. Schultz, Robert J. Morell, Inna A. Belyantseva, Thomas B. Friedman

Journal:

Developmental Biology

Année:

2005

Langue:

english

Fichier:

PDF, 1014 KB

english, 2005

5

Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear

Linda M. Peters, Inna A. Belyantseva, Ayala Lagziel, James F. Battey, Thomas B. Friedman, Robert J. Morell

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 829 KB

english, 2007

6

Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria

Hava Peretz, Meirav Shtauber Naamati, David Levartovsky, Ayala Lagziel, Esther Shani, Ivona Horn, Hanna Shalev, Daniel Landau

Journal:

Molecular Genetics and Metabolism

Année:

2007

Langue:

english

Fichier:

PDF, 663 KB

english, 2007

7

Tricellulin Is a Tight-Junction Protein Necessary for Hearing

Saima Riazuddin, Zubair M. Ahmed, Alan S. Fanning, Ayala Lagziel, Shin-ichiro Kitajiri, Khushnooda Ramzan, Shaheen N. Khan, Parna Chattaraj, Penelope L. Friedman, James M. Anderson, Inna A. Belyantsev

Journal:

The American Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 1.57 MB

english, 2006

8

Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria

Peretz, Hava, Watson, David G., Blackburn, Gavin, Zhang, Tong, Lagziel, Ayala, Shtauber-Naamati, Meirav, Morad, Tova, Keren-Tardai, Elena, Greenshpun, Victoria, Usher, Sali, Shalev, Hanna, Landau, Dan

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 292 KB

english, 2012

9

Expression of CDY1 may identify complete spermatogenesis

Sandra E Kleiman, Ayala Lagziel, Leah Yogev, Amnon Botchan, Gedalia Paz, Haim Yavetz

Journal:

Fertility and Sterility

Année:

2001

Langue:

english

Fichier:

PDF, 364 KB

english, 2001

10

A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction

Lee, Sue I., Conrad, Travis, Jones, Sherri M., Lagziel, Ayala, Starost, Matthew F., Belyantseva, Inna A., Friedman, Thomas B., Morell, Robert J.

Journal:

Hearing Research

Année:

2013

Langue:

english

Fichier:

PDF, 1.49 MB

english, 2013

11

Corrigendum to “A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction” [Hear. Res. 300 (2013) 1–9]

Lee, Sue I., Conrad, Travis, Jones, Sherri M., Lagziel, Ayala, Starost, Matthew F., Belyantseva, Inna A., Friedman, Thomas B., Morell, Robert J.

Journal:

Hearing Research

Année:

2013

Langue:

english

Fichier:

PDF, 130 KB

english, 2013

12

Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

Schultz, Julie M., Yang, Yandan, Caride, Ariel J., Filoteo, Adelaida G., Penheiter, Alan R., Lagziel, Ayala, Morell, Robert J., Mohiddin, Saidi A., Fananapazir, Lameh, Madeo, Anne C., Penniston, John

Journal:

Boston Medical and Surgical Journal

Année:

2005

Langue:

english

Fichier:

PDF, 205 KB

english, 2005

13

Warfarin Therapy is Feasible In CYP2C9*3 Homozygous Patients

Ablin, Jacob, Cabili, Shaltiel, Eldor, Amiram, Lagziel, Ayala, Peretz, Hava

Journal:

Therapeutic Drug Monitoring

Année:

2005

Langue:

english

Fichier:

PDF, 691 KB

english, 2005

14

Recent Advances in the Understanding of Syndromic Forms of Hearing Loss

Friedman, Thomas B., Schultz, Julie M., Ben-Yosef, Tamar, Pryor, Shannon P., Lagziel, Ayala, Fisher, Rachel A., Wilcox, Edward R., Riazuddin, Saima, Ahmed, Zubair M., Belyantseva, Inna A., Griffith, A

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 480 KB

english, 2003

15

Modifier variant of METTL13 suppresses human GAB1–associated profound deafness

Yousaf, Rizwan, Ahmed, Zubair M., Giese, Arnaud P.J., Morell, Robert J., Lagziel, Ayala, Dabdoub, Alain, Wilcox, Edward R., Riazuddin, Sheikh, Friedman, Thomas B., Riazuddin, Saima

Journal:

The Journal of clinical investigation

Année:

2018

Langue:

english

Fichier:

PDF, 17.45 MB

english, 2018