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A case report of complement C4B deficiency in a patient with steroid and IVIG-refractory anti-NMDA receptor encephalitis.

• Authors : Chua GT; Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, Room 106, 1/F, New Clinical Building, 102 Pokfulam Road, Pokfulam, Hong Kong.; Zhou D

Subjects: Anti-N-Methyl-D-Aspartate Receptor Encephalitis/Anti-N-Methyl-D-Aspartate Receptor Encephalitis/Anti-N-Methyl-D-Aspartate Receptor Encephalitis/*therapy ; Complement C4b/Complement C4b/Complement C4b/*genetics ; Immunoglobulins, Intravenous/Immunoglobulins, Intravenous/Immunoglobulins, Intravenous/*therapeutic use

• Source: BMC neurology [BMC Neurol] 2020 Sep 08; Vol. 20 (1), pp. 339. Date of Electronic Publication: 2020 Sep 08.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium:

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Serum complement C4b, fibronectin, and prolidase are associated with the pathological changes of pulmonary tuberculosis.

• Authors : Chong Wang¹ ; Yan-Yuan Li² ; Xiang Li³

• Source: BMC Infectious Diseases. 2014, Vol. 14 Issue 1, p1-17. 17p. 4 Charts, 3 Graphs.

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Complement activation in astrocytomas: deposition of C4d and patient outcome.

• Authors : Mäkelä K; Department of Pathology, University of Tampere Medical School, Tampere, Finland. ; Helén P

Subjects: Astrocytoma/Astrocytoma/Astrocytoma/*immunology ; Brain Neoplasms/Brain Neoplasms/Brain Neoplasms/*immunology ; Complement Activation/Complement Activation/Complement Activation/*immunology

• Source: BMC cancer [BMC Cancer] 2012 Dec 01; Vol. 12, pp. 565. Date of Electronic Publication: 2012 Dec 01.Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium:

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C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism.

• Authors : Sweeten TL; Center for Persons with Disabilities, Utah State University, 6895 Old Main Hill, Logan, UT 84322-6895, USA. ; Odell DW

Subjects: Alleles* ; Genetic Predisposition to Disease* ; Polymorphism, Genetic*

• Source: BMC medical genetics [BMC Med Genet] 2008 Jan 07; Vol. 9, pp. 1. Date of Electronic Publication: 2008 Jan 07.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Targeted deletions of complement lectin pathway genes improve outcome in traumatic brain injury, with MASP-2 playing a major role.

• Authors : Mercurio D; Department of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, 20156, Milan, Italy.; Oggioni M

Subjects: Brain Injuries, Traumatic/Brain Injuries, Traumatic/Brain Injuries, Traumatic/*genetics ; Complement Pathway, Mannose-Binding Lectin/Complement Pathway, Mannose-Binding Lectin/Complement Pathway, Mannose-Binding Lectin/*genetics ; Inflammation/Inflammation/Inflammation/*genetics

• Source: Acta neuropathologica communications [Acta Neuropathol Commun] 2020 Oct 28; Vol. 8 (1), pp. 174. Date of Electronic Publication: 2020 Oct 28.Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Electronic Cited Medium:

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Expression of MMP-2 and TIMP-1 in renal tissue of patients with chronic active antibody-mediated renal graft rejection.

• Authors : Yan Q; Dialysis and Kidney Transplantation Center of PLA, 181 Hospital of PLA, Guilin 541002, China.; Sui W

Subjects: Graft Rejection/Graft Rejection/Graft Rejection/*enzymology ; Kidney/Kidney/Kidney/*enzymology ; Kidney Transplantation/Kidney Transplantation/Kidney Transplantation/*adverse effects

• Source: Diagnostic pathology [Diagn Pathol] 2012 Oct 12; Vol. 7, pp. 141. Date of Electronic Publication: 2012 Oct 12.Publisher: BioMed Central Country of Publication: England NLM ID: 101251558 Publication Model: Electronic Cited Medium:

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Real-time PCR quantification of human complement C4A and C4B genes.

• Authors : Szilagyi A; Institute of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary. ; Blasko B

Subjects: Computer Systems*; Complement C4a/Complement C4a/Complement C4a/*genetics ; Complement C4b/Complement C4b/Complement C4b/*genetics

• Source: BMC genetics [BMC Genet] 2006 Jan 10; Vol. 7, pp. 1. Date of Electronic Publication: 2006 Jan 10.Publisher: BioMed Central Country of Publication: England NLM ID: 100966978 Publication Model: Electronic Cited Medium:

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