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S. Anover · SciRah

Researcher profile · Semantic Scholar

S. Anover

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S. Anover — researcher profile on SciRah

h-index: 3
Works: 11
Citations: 750

Most-cited papers

Analysis of FOXP3 Reveals Multiple Domains Required for Its Function as a Transcriptional Repressor1
Jared E. Lopes, T. Torgerson, L. Schubert, S. Anover +3 more
2006Journal of Immunology288 citations Open access
Semantic Scholar
Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene.
T. Torgerson, Avriel Linane, N. Moes, S. Anover +10 more
2007Gastroenterology256 citations Open access
Semantic Scholar
Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis.
S. Humblet-Baron, Blythe Sather, S. Anover, Shirly Becker-Herman +10 more
2007Journal of Clinical Investigation202 citations Open access
Semantic Scholar
This information is current as Transcriptional Repressor Required for Its Function as a Analysis of FOXP 3 Reveals Multiple Domains and
Jared E. Lopes, T. Torgerson, L. Schubert, S. Anover +3 more
20063 citations
Semantic Scholar
Sa.97. A Unique Mutation in an Upstream Region of the FOXP3 Gene Causes IPEX by Aberrant mRNA Splicing and Lack of FOXP3+ Treg
S. Anover, Avriel Linane, S. Vijay, E. Gambineri +5 more
20062 citations
Semantic Scholar
Clinical, Laboratory, And Molecular Evaluation Of 105 Patients With A Phenotype Of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome
E. Gambineri, M. Hackett, S. Anover, Q. Zhu +3 more
20091 citations Open access
Semantic Scholar
Comèl-Netherton Syndrome - New Insight Into The Molecular Basis of this Rare Syndrome Characterized by Atopic Diathesis and Immune Deficiency
E. Renner, Stacey Rylaarsdam, S. Anover, D. Hartl +10 more
20070 citations Open access
Semantic Scholar
Impaired Humoral Immune Response to a T-Cell-Dependent Neoantigen in Patients with ComèL-Netherton Syndrome
E. Renner, Stacey Rylaarsdam, S. Anover, B. Belohradsky +11 more
20060 citations
Semantic Scholar
Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect
F. Schaffer, J. Cochran, L. Key, T. Chatila +4 more
20060 citations
Semantic Scholar
OR.10. Foxp3 Inhibits Inducible NFAT2 Gene Expression
T. Torgerson, A. Genin, S. Anover, E. Ocheltree +5 more
20060 citations
Semantic Scholar
341. Lentiviral Vector-Mediated Gene Therapy as Treatment for Wiskott-Aldrich Syndrome (WAS): Pre-Clinical Studies in Human Cell Lines and WASp -/- Mice
S. Humblet-Baron, S. Anover, Kevin R. Kipp, Qili Zhu +12 more
20050 citations Open access
Semantic Scholar

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