These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 27839984)

  • 21. Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic Review.
    Sharifinejad N; Jamee M; Zaki-Dizaji M; Lo B; Shaghaghi M; Mohammadi H; Jadidi-Niaragh F; Shaghaghi S; Yazdani R; Abolhassani H; Aghamohammadi A; Azizi G
    Front Immunol; 2020; 11():831. PubMed ID: 32431715
    [No Abstract]   [Full Text] [Related]  

  • 22. Evaluation of the T-cell receptor excision circle assay performances for severe combined immunodeficiency neonatal screening on Guthrie cards in a French single centre study.
    Audrain M; Thomas C; Mirallie S; Bourgeois N; Sebille V; Rabetrano H; Durand-Zaleski I; Boisson R; Persyn M; Pierres C; Mahlaoui N; Fischer A
    Clin Immunol; 2014 Feb; 150(2):137-9. PubMed ID: 24412905
    [No Abstract]   [Full Text] [Related]  

  • 23. ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency.
    Chan AC; Kadlecek TA; Elder ME; Filipovich AH; Kuo WL; Iwashima M; Parslow TG; Weiss A
    Science; 1994 Jun; 264(5165):1599-601. PubMed ID: 8202713
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase.
    Elder ME; Lin D; Clever J; Chan AC; Hope TJ; Weiss A; Parslow TG
    Science; 1994 Jun; 264(5165):1596-9. PubMed ID: 8202712
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Newborn screening for severe T and B cell immunodeficiency in Israel: a pilot study.
    Somech R; Lev A; Simon AJ; Korn D; Garty BZ; Amariglio N; Rechavi G; Almashanu S; Zlotogora J; Etzioni A
    Isr Med Assoc J; 2013 Aug; 15(8):404-9. PubMed ID: 24079059
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel compound heterozygous mutations in ZAP70 in a Chinese patient with leaky severe combined immunodeficiency disorder.
    Liu Q; Wang YP; Liu Q; Zhao Q; Chen XM; Xue XH; Zhou LN; Ding Y; Tang XM; Zhao XD; Zhang ZY
    Immunogenetics; 2017 Apr; 69(4):199-209. PubMed ID: 28124082
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of a novel mutation in ZAP70 and prenatal diagnosis in a Turkish family with severe combined immunodeficiency disorder.
    Karaca E; Karakoc-Aydiner E; Bayrak OF; Keles S; Sevli S; Barlan IB; Yuksel A; Chatila TA; Ozen M
    Gene; 2013 Jan; 512(2):189-93. PubMed ID: 23124046
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.
    Ling E; Broides A; Ling G; Shubinsky G; Hadad N; Nahum A; Simon AJ; Lev A; Somech R
    Immunol Res; 2021 Feb; 69(1):100-106. PubMed ID: 33484432
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Correction of T cell deficiency in ZAP-70 knock-out mice by simple intraperitoneal adoptive transfer of thymocytes.
    Kugyelka R; Kohl Z; Olasz K; Prenek L; Berki T; Balogh P; Boldizsár F
    Clin Exp Immunol; 2018 Jun; 192(3):302-314. PubMed ID: 29431868
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopenia].
    Olbrich P; de Felipe B; Delgado-Pecellin C; Rodero R; Rojas P; Aguayo J; Marquez J; Casanovas J; Sánchez B; Lucena JM; Ybot-Gonzalez P; Borte S; Neth O
    An Pediatr (Barc); 2014 Nov; 81(5):310-7. PubMed ID: 25278007
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole-exome sequencing of T
    El Hawary R; Meshaal S; Mauracher AA; Opitz L; Abd Elaziz D; Lotfy S; Eldash A; Boutros J; Galal N; Pachlopnik Schmid J; Elmarsafy A
    Clin Exp Immunol; 2021 Mar; 203(3):448-457. PubMed ID: 33040328
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Development of population-based newborn screening for severe combined immunodeficiency.
    Chan K; Puck JM
    J Allergy Clin Immunol; 2005 Feb; 115(2):391-8. PubMed ID: 15696101
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Second Tier Testing to Reduce the Number of Non-actionable Secondary Findings and False-Positive Referrals in Newborn Screening for Severe Combined Immunodeficiency.
    Blom M; Pico-Knijnenburg I; Imholz S; Vissers L; Schulze J; Werner J; Bredius R; van der Burg M
    J Clin Immunol; 2021 Nov; 41(8):1762-1773. PubMed ID: 34370170
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Severe combined immunodeficiency due to a defect in the tyrosine kinase ZAP-70.
    Elder ME
    Pediatr Res; 1996 May; 39(5):743-8. PubMed ID: 8726223
    [No Abstract]   [Full Text] [Related]  

  • 35. TREC Based Newborn Screening for Severe Combined Immunodeficiency Disease: A Systematic Review.
    van der Spek J; Groenwold RH; van der Burg M; van Montfrans JM
    J Clin Immunol; 2015 May; 35(4):416-30. PubMed ID: 25893636
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Morpholino-based correction of hypomorphic ZAP70 mutation in an adult with combined immunodeficiency.
    Gavino C; Landekic M; Zeng J; Wu N; Jung S; Zhong MC; Cohen-Blanchet A; Langelier M; Neyret O; Lejtenyi D; Rochefort C; Cotton-Montpetit J; McCusker C; Mazer B; Veillette A; Vinh DC
    J Allergy Clin Immunol; 2017 May; 139(5):1688-1692.e10. PubMed ID: 28216435
    [No Abstract]   [Full Text] [Related]  

  • 37. First reported case of Omenn syndrome in a patient with reticular dysgenesis.
    Henderson LA; Frugoni F; Hopkins G; Al-Herz W; Weinacht K; Comeau AM; Bonilla FA; Notarangelo LD; Pai SY
    J Allergy Clin Immunol; 2013 Apr; 131(4):1227-30, 1230.e1-3. PubMed ID: 23014587
    [No Abstract]   [Full Text] [Related]  

  • 38. Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.
    Borte S; von Döbeln U; Fasth A; Wang N; Janzi M; Winiarski J; Sack U; Pan-Hammarström Q; Borte M; Hammarström L
    Blood; 2012 Mar; 119(11):2552-5. PubMed ID: 22130802
    [TBL] [Abstract][Full Text] [Related]  

  • 39. SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.
    Hauck F; Blumenthal B; Fuchs S; Lenoir C; Martin E; Speckmann C; Vraetz T; Mannhardt-Laakmann W; Lambert N; Gil M; Borte S; Audrain M; Schwarz K; Lim A; Schamel WW; Fischer A; Ehl S; Rensing-Ehl A; Picard C; Latour S
    Clin Immunol; 2015 Dec; 161(2):103-9. PubMed ID: 26187144
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Persistence of natural killer cells with expansion of a hypofunctional CD56-CD16+KIR+NKG2C+ subset in a patient with atypical Janus kinase 3-deficient severe combined immunodeficiency.
    Farnault L; Chambost H; Michel G; Thuret I; de Saint Basile G; Fischer A; Picard C; Picard C; Orlanducci F; Farnarier C; Moretta A; Olive D
    J Allergy Clin Immunol; 2013 Apr; 131(4):1230-3, 1233.e1-2. PubMed ID: 23069490
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.