Y. Valles-Ayoub

发表

On the pathogenesis trail: what marker B cell clones tell us about IBD

S. Targan, L. Gordon, J. Braun, 1994 .

Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry.

Daniel No, D. Darvish, Y. Valles-Ayoub, 2011, Genetic testing and molecular biomarkers.

A VH clonal deficit in human immunodeficiency virus-positive individuals reflects a B-cell maturational arrest.

O. Martínez-Maza, J. Braun, Y. Valles-Ayoub, 1991, Blood.

Serum neural cell adhesion molecule is hyposialylated in hereditary inclusion body myopathy.

Daniel No, D. Darvish, E. Kakkis, 2012, Genetic testing and molecular biomarkers.

Fine-mapping of DNA damage and repair in specific genomic segments

Jonathan Braun, Herman L. Govan, Yadira Valles-Ayoub, 1990, Nucleic Acids Res..

Targeting GNE myopathy: A dual prodrug approach for the delivery of N-acetyl mannosamine 6-phosphate.

Chiara Morozzi, J. Sedlakova, L. Sandoval, 2019, Journal of medicinal chemistry.

Prevalence of GNE p.M712T and hereditary inclusion body myopathy (HIBM) in Sangesar population of Northern Iran

D. Darvish, L. Sandoval, J. Urtizberea, 2013, Clinical genetics.

Novel GNE mutations in autosomal recessive hereditary inclusion body myopathy patients.

M. Tarnopolsky, Daniel No, T. Mozaffar, 2013, Genetic Testing and Molecular Biomarkers.

Mixed Inbred FVB;B6 Background Strain Attenuates Kidney Disease and Improves Survival of Gne M712T/M712T Mice

O. Scremin, G. Lawson, D. Darvish, 2012 .

New diagnostic method for lysosomal acid lipase deficiency and the need to recognize its manifestation in infants (Wolman disease).

K. Sims, R. Tripuraneni, M. C. Gallegos-Rivas, 2015, Journal of pediatric gastroenterology and nutrition.

Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent.

J. Mendell, Daniel No, C. Morel, 2010, Genetic testing and molecular biomarkers.

Validation of GNE:p.M712T identification by melting curve analysis.

M. Neshat, D. Darvish, Y. Valles-Ayoub, 2008, Genetic testing.

MTHFR C677T genotype frequency in patients of Middle Eastern descent as determined by real-time PCR and melting curve analysis.

D. Darvish, Y. Valles-Ayoub, Saghi Esfandiarifard, 2009, Genetic testing and molecular biomarkers.

Expression of a novel autoantibody defined by the VH3-15 gene in inflammatory bowel disease and Campylobacter jejuni enterocolitis.

S. Targan, L. Gordon, J. Braun, 1994, Journal of immunology.