Safety and Biodistribution of an Autologous Bone Marrow‐Derived Mononuclear Cell Infusion into Renal Arteries in Patients with Focal Segmental Glomerulosclerosis: A Phase 1 Study.

Autor: Botelho, Bruno Freire¹ (AUTHOR), Barreira, André Luis¹ (AUTHOR), Filippo, Marcio Gomes² (AUTHOR), Asensi, Karina Dutra³ (AUTHOR), Faccioli, Lanuza A P³ (AUTHOR), dos Santos Salgado, Anna Beatriz³ (AUTHOR), de Salles, Elizabeth Figueiredo⁴ (AUTHOR), Marques, Carlos Eduardo Cruz⁴ (AUTHOR), Silva, Pedro Leme⁵ (AUTHOR), dos Santos Goldenberg, Regina Coeli⁶ (AUTHOR), Maiolino, Angelo⁷ (AUTHOR), Gutfilen, Bianca⁴ (AUTHOR), de Souza, Sergio Augusto Lopes⁴ (AUTHOR), Junior, Maurilo Leite¹ (AUTHOR), Morales, Marcelo Marcos⁸ (AUTHOR) mmorales@biof.ufrj.br, Rahman, Md Shaifur (AUTHOR) mdshaifur@baec.gov.bd

Publikováno v: Stem Cells International. 7/9/2024, Vol. 2024, p1-11. 11p.

The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10

Autor: J S, Wu, N L, Carson, S, Myers, A J, Pakstis, J R, Kidd, C M, Castiglione, L, Anderson, L S, Hoyle, M, Genel, M, Verdy

Publikováno v: American journal of human genetics. 46(3)

Multiple endocrine neoplasia type 2A (MEN2A) is a rare cancer syndrome that is inherited in an apparently autosomal dominant fashion. Previous linkage studies had assigned the MEN2A locus to chromosome 10 in the pericentromeric region. We recently ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::193e16cc31a5b725b4f2e4bbae6225a5
https://pubmed.ncbi.nlm.nih.gov/1968709

Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion region

Autor: K K, Kidd, J R, Kidd, C M, Castiglione, A J, Pakstis, R S, Sparkes

Publikováno v: Genetic epidemiology. 3(3)

In an earlier paper, positive but nonsignificant lod scores were found in pair-wise linkage tests between multiple endocrine neoplasia type 2A (MEN-2A) and both the haptoglobin (HP) locus on chromosome 16 and group-specific component (GC) locus on ch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b70d4b6364d867b43379d1c9aeac5d20
https://pubmed.ncbi.nlm.nih.gov/2873080

The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1

Autor: K K, Kidd, J R, Kidd, C M, Castiglione, R S, Sparkes, J A, Egeland, E, Bakker

Publikováno v: Human heredity. 38(1)

D1S2 was one of the first restriction fragment length polymorphisms (RFLPs) assigned to chromosome 1, but its regional location was unknown. In this paper we present data that place this RFLP into both the genetic map and the physical-cytogenetic map

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d6c79c716d1a1953fc857d3209ddd1c7
https://pubmed.ncbi.nlm.nih.gov/2895061

Reversible and Fast (De)fluorination of High‐Capacity Cu2O Cathode: One Step Toward Practically Applicable All‐Solid‐State Fluoride‐Ion Battery.

Autor: Zhang, Datong, Yamamoto, Kentaro, Wang, Yanchang, Gao, Shenghan, Uchiyama, Tomoki, Watanabe, Toshiki, Takami, Tsuyoshi, Matsunaga, Toshiyuki, Nakanishi, Koji, Miki, Hidenori, Iba, Hideki, Amezawa, Koji, Maeda, Kazuhiko, Kageyama, Hiroshi, Uchimoto, Yoshiharu

Publikováno v: Advanced Energy Materials; 12/2/2021, Vol. 11 Issue 45, p1-9, 9p