A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion.

Paranjape, Neha; Lin, Yu-Hsiu T; Flores-Ramirez, Quetzal; Sarin, Vishesh; Johnson, Amanda Brooke; Chu, Julia; Paredes, Mercedes; Wiita, Arun P

Paranjape, Neha; Lin, Yu-Hsiu T; Flores-Ramirez, Quetzal; Sarin, Vishesh; Johnson, Amanda Brooke; Chu, Julia; Paredes, Mercedes; Wiita, Arun P.

Afiliação

Paranjape N; Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA, USA.
Lin YT; Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA, USA.
Flores-Ramirez Q; University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Sarin V; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.
Johnson AB; Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA, USA.
Chu J; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.
Paredes M; San Francisco State University, San Francisco, CA, USA.
Wiita AP; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.

Sci Rep ; 13(1): 7689, 2023 05 11.

Article em En | MEDLINE | ID: mdl-37169815

Assuntos

Síndrome de DiGeorge; Animais; Camundongos; Humanos; Síndrome de DiGeorge/genética; Estruturas Cromossômicas; Heterogeneidade Genética; Neurônios; Deleção Cromossômica; Cromossomos Humanos Par 22/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

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