Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jalaja Sukumaran"'
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
Abstract Background The frequency of the alpha thalassemia trait is approximately 40% in the Kuwaiti population, but there has been no comprehensive study of the prevalent alleles. This is a report of patients who were referred for molecular diagnosi
Externí odkaz:
https://doaj.org/article/99c2a2f12e884a2ca99aa806329829b6
Publikováno v:
BMC Rheumatology, Vol 2, Iss 1, Pp 1-6 (2018)
Abstract Background Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease which involves the loss of self-tolerance with hyperactivation of autoreactive T- and B-cells. Protein tyrosine phosphatase non-receptor type 22 (PTPN22) enc
Externí odkaz:
https://doaj.org/article/f2af9300af824c99b4b333196c03d8a2
Autor:
Adel M. Al-Awadhi, Mohammad Z. Haider, Aminah M. Al-Awadi, Anita K. Kalarikkal, Jalaja Sukumaran, Eman A. H. Hasan, Youssef Bartella
Publikováno v:
Open Journal of Rheumatology and Autoimmune Diseases. 12:99-113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bf939da53f302fcf77b4b7bc8e472cc
https://doi.org/10.4236/ojra.2022.124011
https://doi.org/10.4236/ojra.2022.124011
Publikováno v:
The Open Rheumatology Journal. 15:45-50
Background: Rheumatoid Arthritis (RA) is a chronic disorder characterized by an inflammation of synovial tissue in joints resulting in pain, deformities and affects the quality of life. The gene for protein tyrosine phosphatase non-receptor type 22 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e5910d1f166f727a5418c1096da8e5f
https://doi.org/10.2174/1874312902115010045
https://doi.org/10.2174/1874312902115010045
Autor:
Youssef Bartella, Asiya T. Mohammed, Jalaja Sukumaran, Eman Hasan, Adel Al-Awadhi, Mohammad Z. Haider
Publikováno v:
The Open Rheumatology Journal. 14:15-21
Background: Psoriatic arthritis (PsA) is a chronic, systemic inflammatory arthritic disease characterized by joint inflammation that is associated with cutaneous psoriasis, and can lead to pain, swelling, or stiffness in one or more joints. It result
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ef78420d90b55fcf3e571ffa9927cf6
https://doi.org/10.2174/1874312902014010015
https://doi.org/10.2174/1874312902014010015
Autor:
Rasha Al Khaldi, Maria Jinky Fernandez, Adekunle Adekile, Nagihan Akbulut-Jeradi, Jalaja Sukumaran
Publikováno v:
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 567, p 567 (2021)
Volume 11
Issue 6
Journal of Personalized Medicine, Vol 11, Iss 567, p 567 (2021)
Volume 11
Issue 6
Patients with sickle cell disease (SCD) in Kuwait have elevated HbF levels ranging from ~10–44%
however, the modulating factors are unclear. We investigated the association of single nucleotide polymorphisms (SNPs) at BCL11A, HBS1L-MYB and HBB
however, the modulating factors are unclear. We investigated the association of single nucleotide polymorphisms (SNPs) at BCL11A, HBS1L-MYB and HBB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91877fdb4f1ad12903299d19eda15521
https://pubmed.ncbi.nlm.nih.gov/34204365
https://pubmed.ncbi.nlm.nih.gov/34204365
Autor:
Nagihan Akbulut-Jeradi, Rasha Al Khaldi, Adekunle Adekile, Jalaja Sukumaran, Maria Jinky Fernandez
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 454, p 454 (2021)
Journal of Personalized Medicine
Volume 11
Issue 6
Journal of Personalized Medicine
Volume 11
Issue 6
Hemoglobin genotype and HBB haplotype are established genetic factors that modify the clinical phenotype in sickle cell disease (SCD). Current methods of establishing these two factors are cumbersome and/or prone to errors. The throughput capability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc9669ff8e1c64896fe398376c5e50b
https://www.mdpi.com/2075-4426/11/6/454
https://www.mdpi.com/2075-4426/11/6/454
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background The frequency of the alpha thalassemia trait is approximately 40% in the Kuwaiti population, but there has been no comprehensive study of the prevalent alleles. This is a report of patients who were referred for molecular diagnosis over a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324f29d1a40a5a5009eae9c8df257a69
https://doi.org/10.21203/rs.2.22547/v5
https://doi.org/10.21203/rs.2.22547/v5
Autor:
Mohammed Al-Kandari, Adekunle Adekile, Mark D’Souza, Jalaja Sukumaran, Mohammad Z. Haider, Marouf Rajaa
Publikováno v:
Medical Principles and Practice. 16:286-290
Objective: This study aimed to document the transition of hemoglobin (Hb) F levels from early childhood to adulthood in Kuwaiti sickle cell disease patients, investigating its relationship to sex, Hb genotype and coexistence of α-thalassemia trait.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15762fa36ef5a7af4e19d3bc1ffe8687
https://doi.org/10.1159/000102151
https://doi.org/10.1159/000102151
Autor:
Sukhbir S, Uppal, Mohammad Z, Haider, Sawsan J, Hayat, Mini, Abraham, Jalaja, Sukumaran, Gursev S, Dhaunsi
Publikováno v:
The Journal of rheumatology. 34(12)
Only 30% of the genetic contribution to rheumatoid arthritis (RA) can be attributed to HLA genes, and other non-HLA genes may play a role in RA susceptibility. Angiotensin-converting enzyme (ACE) has been reported to be involved in pathogenesis of RA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d51a4a0cee2c7818b61df1bbaa4210ff
https://pubmed.ncbi.nlm.nih.gov/17985406
https://pubmed.ncbi.nlm.nih.gov/17985406