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Antiproliferative Oleanane Saponins from Dizygotheca elegantissima

Autor: Nicola Malafronte, M. Pesca, Antonio Vassallo, Letizia Ambrosio, Dal Piaz F, N. D. Melle, Lorella Severino

Publikováno v: Scopus-Elsevier

Four new oleanane saponins (1-4), together with three known saponins, were isolated from the aerial parts of Dizygotheca elegantissima R. Vig. & Guillaumin. Their structures were elucidated by 1D and 2D NMR experiments including 1D TOCSY, DQF-COSY, H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13a92f9d545793ff2a35d37e3f4fb996
http://hdl.handle.net/11588/516691

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Akademický článek

Single-cell peripheral immunoprofiling of lewy body and Parkinson's disease in a multi-site cohort.

Autor: Phongpreecha, Thanaphong^1,2,3 (AUTHOR), Mathi, Kavita⁴ (AUTHOR), Cholerton, Brenna¹ (AUTHOR), Fox, Eddie J.¹ (AUTHOR), Sigal, Natalia⁴ (AUTHOR), Espinosa, Camilo^2,3,5 (AUTHOR), Reincke, Momsen^2,3,5 (AUTHOR), Chung, Philip² (AUTHOR), Hwang, Ling-Jen³ (AUTHOR), Gajera, Chandresh R.¹ (AUTHOR), Berson, Eloise^1,2,3 (AUTHOR), Perna, Amalia¹ (AUTHOR), Xie, Feng^2,3,5 (AUTHOR), Shu, Chi-Hung^2,3,5 (AUTHOR), Hazra, Debapriya^2,3,5 (AUTHOR), Channappa, Divya⁶ (AUTHOR), Dunn, Jeffrey E.⁶ (AUTHOR), Kipp, Lucas B.⁶ (AUTHOR), Poston, Kathleen L.⁶ (AUTHOR), Montine, Kathleen S.¹ (AUTHOR)

Publikováno v: Molecular Neurodegeneration. 8/1/2024, Vol. 19 Issue 1, p1-13. 13p.

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Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus

Publikováno v: Human Genetics. 86:355-358

A total of 252 chromosomes from 126 patients with phenylalanine hydroxylase (PAH) deficiencies were analyzed for both mutant genotypes and restriction fragment length polymorphism (RFLP) haplotypes at the PAH locus. The mutant genes studied originate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca9c892fe8064eb522e05158b236ef7f
https://doi.org/10.1007/bf00201832

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Akademický článek

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Differential expression profiling of head and neck squamous cell carcinoma (HNSCC)

Autor: L. Bracco, F Lemaire, Julia Young, Régine Millon, Inès Schultz, Anne Cromer, Joseph Abecassis, Changqi Zhao, Christine Wasylyk, D Melle, Bohdan Wasylyk, Danièle Muller, P. Marchal

Publikováno v: British Journal of Cancer

Head and neck squamous cell carcinoma (HNSCC) is the fifth most common cancer in men with an incidence of about 780000 new cases per year worldwide and a poor rate of survival. There is a need for a better understanding of HNSCC, for the development

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85c076b31e708db993b848999ad2a141
https://pubmed.ncbi.nlm.nih.gov/14612907

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Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria

Autor: Françoise Rey, Arnold Munnich, Paule Bénit, D. Melle, Jean Rey

Publikováno v: Human Mutation. 4:229-231

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2508f36c8fa73cdd6221409bf0d647fd
https://doi.org/10.1002/humu.1380040311

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Two distinct mutations at a single BamHI site in phenylketonuria

Autor: Baudouin François, P Verelst, Arnold Munnich, Stanislas Lyonnet, M. Berthelon, D. Melle, Françoise Rey

Publikováno v: Journal of Medical Genetics. 28:38-40

Classical phenylketonuria is an autosomal recessive disease caused by a deficiency of hepatic phenylalanine hydroxylase (PAH). The abolition of an invariant BamHI site located in the coding sequence of the PAH gene (exon 7) led to the recognition of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66f8103dbd7bda28ffb306ee3ab34ae6
https://doi.org/10.1136/jmg.28.1.38

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