T Cell Transcriptome in Chromosome 22q11.2 Deletion Syndrome.

Raje, Nikita R; Noel-MacDonnell, Janelle R; Shortt, Katherine A; Gigliotti, Nicole M; Chan, Marcia A; Heruth, Daniel P

Raje, Nikita R; Noel-MacDonnell, Janelle R; Shortt, Katherine A; Gigliotti, Nicole M; Chan, Marcia A; Heruth, Daniel P.

Afiliação

Raje NR; Division of Allergy, Immunology, Pulmonary and Sleep Medicine, Children's Mercy Kansas City, Kansas City, MO; nraje@cmh.edu.
Noel-MacDonnell JR; Department of Pediatrics, Children's Mercy Kansas City, University of Missouri Kansas City School of Medicine, Kansas City, MO.
Shortt KA; Department of Pediatrics, Children's Mercy Kansas City, University of Missouri Kansas City School of Medicine, Kansas City, MO.
Gigliotti NM; Department of Health Services and Outcomes Research, Children's Mercy Kansas City, Kansas City, MO.
Chan MA; Precision Genomics, Intermountain Healthcare, St. George, UT; and.
Heruth DP; Department of Pediatrics, Children's Mercy Kansas City, University of Missouri Kansas City School of Medicine, Kansas City, MO.

J Immunol ; 209(5): 874-885, 2022 09 01.

Article em En | MEDLINE | ID: mdl-35940635

Assuntos

Síndrome de DiGeorge; Linfopenia; Cromossomos; Síndrome de DiGeorge/genética; Humanos; Receptores X do Fígado/genética; Linfopenia/genética; Receptores X de Retinoides/genética; Linfócitos T; Transcriptoma

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Linfopenia Limite: Humans Idioma: En Revista: J Immunol Ano de publicação: 2022 Tipo de documento: Article

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