Expanding the clinical phenotype of <scp>FADD</scp> deficiency with a novel mutation and its role in Fas‐mediated apoptotic pathway-Reference-Cited by-同舟云学术

Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas‐mediated apoptotic pathway

Published:2023-05-18 Issue:2 Volume:202 Page:
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Setia Priyanka¹^ORCID,Bargir Umair Ahmed¹^ORCID,Shanmukhaiah Chandrakala²,Jodhawat Neha¹^ORCID,Gaikwad Pallavi¹^ORCID,Vedpathak Disha¹,Dutta Shubhankar³,Kulkarni Rucha³⁴,Kambli Priyanka¹^ORCID,Dalvi Aparna¹,Shinde Shweta¹,Gupta Maya¹,Nambiar Nayana¹,Sawant Sneha¹^ORCID,Shelar Shraddha¹,Dhawale Amruta¹,Mohanty Madhu⁵,Yadav Reetika Malik¹^ORCID,Bose Kakoli³⁴,Madkaikar Manisha¹^ORCID

Affiliation:

1. Department of Paediatric Immunology and Leukocyte Biology ICMR‐National Institute of Immunohaematology (NIIH) Mumbai India

2. Department of Haematology King Edward Memorial Hospital Mumbai India

3. Integrated Biophysics and Structural Biology Lab Advanced Centre for Treatment Research and Education in Cancer, Tata Memorial Centre (ACTREC) Navi Mumbai India

4. Homi Bhabha National Institute (HBNI) BARC Training School Complex Mumbai India

5. ICMR‐NIV Mumbai unit (ERC) Haffkine Institute Compound Mumbai India

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.18871

Reference13 articles.

1. Autoimmune Lymphoproliferative Syndrome: an Update and Review of the Literature

2. A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS

3. Whole-Exome-Sequencing-Based Discovery of Human FADD Deficiency

4. A new case of Fas-associated death domain protein deficiency and update on treatment outcomes

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