Sali Usher : rechercher sur Z-Library

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1

Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews

David B. Goldstein, David E. Reich, Neil Bradman, Sali Usher, Uri Seligsohn, Hava Peretz

Journal:

The American Journal of Human Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 72 KB

english, 1999

2

A 14-bp deletion (codon 554 del AAGgtaacagagtg) at exon 14/intron N junction of the coagulation factor XI gene disrupts splicing and causes severe factor XI deficiency

Hava Peretz, Ariella Zivelin, Saly Usher, Uri Seligsohn

Journal:

Année:

1996

Langue:

english

Fichier:

PDF, 231 KB

english, 1996

3

Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting

Hava Peretz, Rafael Luboshitsky, Ela Baron, Amnon Biton, Ruth Gershoni, Saly Usher, Elisheva Grynberg, Emanuel Yakobson, Eran Graff, Mordechai Lapidot

Journal:

Année:

1997

Langue:

english

Fichier:

PDF, 142 KB

english, 1997

4

Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure–function correlations of αIIbβ3 integrin (ITGA2B, ITGB3)

Hava Peretz, Nurit Rosenberg, Meytal Landau, Saly Usher, Everette J.R. Nelson, Ronit Mor-Cohen, Deborah L. French, Beau W. Mitchell, Sukesh C. Nair, Mammen Chandy, Barry S. Coller, Alok Srivastava, Ur

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 420 KB

english, 2006

5

Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17

Deborah L. French, Barry S. CP, , er, Saly Usher, Richard Berkowitz, Christine Eng, Uri Seligsohn, Hava Peretz

Journal:

British Journal of Haematology

Année:

1998

Langue:

english

Fichier:

PDF, 422 KB

english, 1998

6

Current strategy for genetic analysis of haemophilia A families

RIMA DARDIK, HAVA PERETZ, SALI USHER, URI SELIGSOHN, URI MARTINOWITZ

Journal:

Année:

1996

Langue:

english

Fichier:

PDF, 573 KB

english, 1996

7

Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis

Einor Ben Assayag, Shani Shenhar-Tsarfaty, Irena Bova, Shlomo Berliner, Sali Usher, Hava Peretz, Itzhak Shapira, Natan M. Bornstein

Journal:

Thrombosis Research

Année:

2009

Langue:

english

Fichier:

PDF, 219 KB

english, 2009

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

Gender differences in the expression of erythrocyte aggregation in relation to Bβ-fibrinogen gene polymorphisms in apparently healthy individuals

Assayag, Einor, Bova, Irena, Berliner, Shlomo, Peretz, Hava, Usher, Sali, Shapira, Itzhak, Bornstein, Natan

Journal:

Thrombosis and Haemostasis

Année:

2006

Langue:

english

Fichier:

PDF, 812 KB

english, 2006

10

The Price of Stress: High Bedtime Salivary Cortisol Levels Are Associated with Brain Atrophy and Cognitive Decline in Stroke Survivors. Results from the TABASCO Prospective Cohort Study

Tene, Oren, Hallevi, Hen, Korczyn, Amos D., Shopin, Ludmila, Molad, Jeremy, Kirschbaum, Clemens, Bornstein, Natan M., Shenhar-Tsarfaty, Shani, Kliper, Efrat, Auriel, Eitan, Usher, Sali, Stalder, Tobia

Journal:

Journal of Alzheimer's Disease

Année:

2018

Langue:

english

Fichier:

PDF, 251 KB

english, 2018

11

An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the AfroâAsian stoneâforming belt

Peretz, Hava, Korostishevsky, Michael, Steinberg, David M., Kabha, Mustafa, Usher, Sali, Krause, Irit, Shalev, Hannah, Landau, Daniel, Levartovsky, David

Journal:

Année:

2020

Langue:

english

Fichier:

PDF, 1.48 MB

english, 2020

12

The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin

Peretz, Hava, Mulai, Avital, Usher, Sali, Zivelin, Ariella, Segal, Avihai, Weisman, Zahavi, Mittelman, Moshe, Lupo, Hannah, Lanir, Naomi, Brenner, Benjamin, Shpilberg, Ofer, Seligsohn, Uri

Journal:

Année:

1997

Fichier:

PDF, 262 KB

1997