نتائج البحث

HTRA1 methylation in peripheral blood as a potential marker for the preclinical detection of stroke: a case–control study and a prospective nested case–control study.

• Authors : Liu, Chunlan¹ (AUTHOR); Li, Mengxia¹ (AUTHOR); Yin, Qiming¹ (AUTHOR)

• Source: Clinical Epigenetics. 12/29/2022, Vol. 14 Issue 1, p1-13. 13p.

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Novel heterozygous HTRA1 pathogenic variant found in a Chinese family with autosomal dominant cerebral small vessel Disease.

• Authors : Wu, Changzhu¹; Chen, Long²; Ke, Shaofa³

• Source: Annals of Indian Academy of Neurology. Nov/Dec2020, Vol. 23 Issue 6, p832-835. 4p.

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A new Chinese family with HTRA1 mutation associated with CARASIL.

• Authors : Sun D; Department of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, China.

Subjects: Leukoencephalopathies*/Leukoencephalopathies*/Leukoencephalopathies*/diagnostic imaging ; Leukoencephalopathies*/Leukoencephalopathies*/Leukoencephalopathies*/genetics ; Spinal Diseases*/Spinal Diseases*/Spinal Diseases*/geneticsCerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

• Source: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2022 Jul; Vol. 43 (7), pp. 4577-4579. Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Novel mutations in HTRA1‐related cerebral small vessel disease and comparison with CADASIL.

• Authors : Zhang, Chen¹ (AUTHOR); Zheng, Honghua² (AUTHOR); Li, Xin² (AUTHOR)

• Source: Annals of Clinical & Translational Neurology. Oct2022, Vol. 9 Issue 10, p1586-1595. 10p.

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Genes associated with inflammation and the cell cycle may serve as biomarkers for the diagnosis and prognosis of acute myocardial infarction in a Chinese population.

• Authors : Su, Jiang¹; Gao, Changqing¹ ; Wang, Rong¹

• Source: Molecular Medicine Reports. Aug2018, Vol. 18 Issue 2, p1311-1322. 12p. 5 Charts, 6 Graphs.

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Association of Specific Genetic Polymorphisms with Age-related Macular Degeneration in a Northern Chinese Population.

• Authors : Zhuang, Wenjuan¹ (AUTHOR); Li, HuiPing¹ (AUTHOR); Liu, Yani¹ (AUTHOR)

• Source: Ophthalmic Genetics. Sep2014, Vol. 35 Issue 3, p156-161. 6p.

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Joint Effect of CFH and ARMS2/HTRA1 Polymorphisms on Neovascular Age-Related Macular Degeneration in Chinese Population.

• Authors : Fang, Kai¹ ; Gao, Pei¹ ; Tian, Jun¹

• Source: Journal of Ophthalmology. 3/25/2015, Vol. 2015, p1-8. 8p.

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Genetic and functional dissection of ARMS2 in age-related macular degeneration and polypoidal choroidal vasculopathy.

• Authors : Cheng Y; Department of Ophthalmology, People's Hospital, Peking University, Beijing, China.; Huang L

Subjects: Choroidal Neovascularization/Choroidal Neovascularization/Choroidal Neovascularization/*genetics ; Macular Degeneration/Macular Degeneration/Macular Degeneration/*genetics ; Proteins/Proteins/Proteins/*genetics

• Source: PloS one [PLoS One] 2013; Vol. 8 (1), pp. e53665. Date of Electronic Publication: 2013 Jan 09.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Genetic association with response to intravitreal ranibizumab for neovascular age-related macular degeneration in the Han Chinese population.

• Authors : Yuan D; Department of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, PR China.; Yuan D

Subjects: Polymorphism, Single Nucleotide*; Angiogenesis Inhibitors/Angiogenesis Inhibitors/Angiogenesis Inhibitors/*therapeutic use ; Antibodies, Monoclonal, Humanized/Antibodies, Monoclonal, Humanized/Antibodies, Monoclonal, Humanized/*therapeutic use

• Source: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde [Ophthalmologica] 2013; Vol. 230 (4), pp. 227-32. Date ofPublisher: Karger Country of Publication: Switzerland NLM ID: 0054655 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1423-0267

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Age-related macular degeneration-susceptibility single nucleotide polymorphisms in a han chinese control population.

• Authors : Hu J; Department of Ophthalmology, Affiliated Hospital of Nantong University, Jiangsu Province, China.; Yuan Y

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Asian People/Asian People/Asian People/*ethnology

• Source: Ophthalmic epidemiology [Ophthalmic Epidemiol] 2011 Jun; Vol. 18 (3), pp. 137-42.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9435674 Publication Model: Print Cited Medium: Internet ISSN: 1744-5086

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