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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1978 3
1979 2
1980 3
1981 2
1982 2
1983 1
1984 2
1985 2
1986 5
1987 2
1988 3
1989 1
1990 4
1991 1
1992 1
1994 2
1996 2
1997 3
1998 4
1999 2
2000 13
2001 15
2002 10
2003 9
2004 11
2005 8
2006 6
2007 3
2008 3
2009 1
2010 7
2011 5
2012 6
2013 3
2014 4
2015 2
2016 2
2017 4
2018 2
2019 1
2020 5
2021 10
2022 3
2023 4
2024 1

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176 results

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Page 1
ABC Family Transporters.
Liu X. Liu X. Adv Exp Med Biol. 2019;1141:13-100. doi: 10.1007/978-981-13-7647-4_2. Adv Exp Med Biol. 2019. PMID: 31571164 Review.
Several human diseases such as cystic fibrosis, sitosterolemia, Tangier disease, intrahepatic cholestasis, and retinal degeneration are associated with mutations in corresponding transporters. ...
Several human diseases such as cystic fibrosis, sitosterolemia, Tangier disease, intrahepatic cholestasis, and retinal degener …
Coronavirus disease 2019 (COVID-19): An overview of the immunopathology, serological diagnosis and management.
Anka AU, Tahir MI, Abubakar SD, Alsabbagh M, Zian Z, Hamedifar H, Sabzevari A, Azizi G. Anka AU, et al. Scand J Immunol. 2021 Apr;93(4):e12998. doi: 10.1111/sji.12998. Epub 2020 Dec 3. Scand J Immunol. 2021. PMID: 33190302 Free PMC article. Review.
SARS-CoV-2 is a novel human coronavirus responsible for the Coronavirus disease 2019 (COVID-19) pandemic. Pneumonia and acute respiratory distress syndrome are the major complications of COVID-19. SARS-CoV-2 infection can activate innate and adaptive immune responses and r …
SARS-CoV-2 is a novel human coronavirus responsible for the Coronavirus disease 2019 (COVID-19) pandemic. Pneumonia and acute respira …
Interleukin-18 cytokine in immunity, inflammation, and autoimmunity: Biological role in induction, regulation, and treatment.
Ihim SA, Abubakar SD, Zian Z, Sasaki T, Saffarioun M, Maleknia S, Azizi G. Ihim SA, et al. Front Immunol. 2022 Aug 11;13:919973. doi: 10.3389/fimmu.2022.919973. eCollection 2022. Front Immunol. 2022. PMID: 36032110 Free PMC article. Review.
Its elevated levels have been reported in the blood of patients with some immune-related diseases, including rheumatoid arthritis, systemic lupus erythematosus, type I diabetes mellitus, atopic dermatitis, psoriasis, and inflammatory bowel disease. In the present review, w …
Its elevated levels have been reported in the blood of patients with some immune-related diseases, including rheumatoid arthritis, systemic …
Peripheral neuropathy in Tangier disease: A literature review and assessment.
Mercan M, Yayla V, Altinay S, Seyhan S. Mercan M, et al. J Peripher Nerv Syst. 2018 Jun;23(2):88-98. doi: 10.1111/jns.12265. Epub 2018 May 8. J Peripher Nerv Syst. 2018. PMID: 29582519 Review.
Tangier disease (TD) (OMIM#205400) is a rare cause of inherited metabolic neuropathies characterized by marked deficiency of high-density lipoproteins and accumulation of cholesterol esters in various tissue resulting from reverse cholesterol transport deficiency. . …
Tangier disease (TD) (OMIM#205400) is a rare cause of inherited metabolic neuropathies characterized by marked deficiency of h …
Current Diagnosis and Management of Tangier Disease.
Koseki M, Yamashita S, Ogura M, Ishigaki Y, Ono K, Tsukamoto K, Hori M, Matsuki K, Yokoyama S, Harada-Shiba M. Koseki M, et al. J Atheroscler Thromb. 2021 Aug 1;28(8):802-810. doi: 10.5551/jat.RV17053. Epub 2021 May 14. J Atheroscler Thromb. 2021. PMID: 33994407 Free PMC article. Review.
Tangier disease is a genetic disorder characterized by an absence or extremely low level of high-density lipoprotein (HDL)-cholesterol (HDL-C). ...With dysfunctional mutations in both alleles (homozygotes or compound heterozygotes), the HDL-C level is mostly less th …
Tangier disease is a genetic disorder characterized by an absence or extremely low level of high-density lipoprotein (HDL)-cho …
Orphan Peripheral Neuropathies.
Finsterer J, Löscher WN, Wanschitz J, Iglseder S. Finsterer J, et al. J Neuromuscul Dis. 2021;8(1):1-23. doi: 10.3233/JND-200518. J Neuromuscul Dis. 2021. PMID: 32986679 Free PMC article. Review.
METHODS: Literature reviewResults:Rareness of diseases is not uniformly defined but in the US an orphan disease is diagnosed if the prevalence is <1:200000, in Europe if <5:10000. ...TMEM240), hereditary spastic paraplegias (e.g UBAP1), lysosomal storage disease …
METHODS: Literature reviewResults:Rareness of diseases is not uniformly defined but in the US an orphan disease is diagnosed if the p …
HDL genetic defects.
Nair DR, Nair A, Jain A. Nair DR, et al. Curr Pharm Des. 2014;20(40):6230-7. doi: 10.2174/1381612820666140620122412. Curr Pharm Des. 2014. PMID: 24953397 Review.
Inheritance of a Milano mutation of apolipoprotein A1 decreases the risk of atherosclerotic disease despite low circulating levels of HDL-C. Tangier disease and Fish Eye disease are caused by mutations in the ATP binding cassette A1 (ABCA1), a transpor …
Inheritance of a Milano mutation of apolipoprotein A1 decreases the risk of atherosclerotic disease despite low circulating levels of …
The ABCs of Sterol Transport.
Plummer AM, Culbertson AT, Liao M. Plummer AM, et al. Annu Rev Physiol. 2021 Feb 10;83:153-181. doi: 10.1146/annurev-physiol-031620-094944. Epub 2020 Nov 3. Annu Rev Physiol. 2021. PMID: 33141631 Review.
ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to disorders such as Tangier disease and sitosterolemia. Biochemical and structural information on ABC sterol transporters is beginni …
ATP-binding cassette (ABC) transporters play several critical roles in this process, and mutations in these sterol transporters lead to diso …
Features and roles of T helper 22 cells in immunological diseases and malignancies.
Hossein-Khannazer N, Zian Z, Bakkach J, Kamali AN, Hosseinzadeh R, Anka AU, Yazdani R, Azizi G. Hossein-Khannazer N, et al. Scand J Immunol. 2021 May;93(5):e13030. doi: 10.1111/sji.13030. Epub 2021 Feb 22. Scand J Immunol. 2021. PMID: 33576072 Free article. Review.
Although, new studies showed that both Th22 and IL-22 are closely associated with the pathogenesis of inflammatory, autoimmune and allergic disease as well as malignancies. In this review, we aim to describe the development and characteristics of Th22 cells as well as thei …
Although, new studies showed that both Th22 and IL-22 are closely associated with the pathogenesis of inflammatory, autoimmune and allergic …
Tangier disease and ABCA1.
Oram JF. Oram JF. Biochim Biophys Acta. 2000 Dec 15;1529(1-3):321-30. doi: 10.1016/s1388-1981(00)00157-8. Biochim Biophys Acta. 2000. PMID: 11111099 Review.
Tangier disease is an autosomal recessive genetic disorder characterized by a severe high-density lipoprotein (HDL) deficiency, sterol deposition in tissue macrophages, and prevalent atherosclerosis. Mutations in the ATP binding cassette transporter ABCA1 cause T …
Tangier disease is an autosomal recessive genetic disorder characterized by a severe high-density lipoprotein (HDL) deficiency …
176 results