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1.
Genetic features and kidney morphological changes in women with X-linked Alport syndrome.
J Med Genet;
60(12): 1169-1176, 2023 Nov 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-37225412
2.
Clinical Implications of a New DDX58 Pathogenic Variant That Causes Lupus Nephritis due to RIG-I Hyperactivation.
J Am Soc Nephrol;
34(2): 258-272, 2023 02 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36261300
3.
Dissecting the genotype-phenotype correlation of COL4A5 gene mutation and its response to renin-angiotensin-aldosterone system blockers in Chinese male patients with Alport syndrome.
Nephrol Dial Transplant;
37(12): 2487-2495, 2022 11 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-35020912
4.
The COL4A3 and COL4A4 Digenic Mutations in cis Result in Benign Familial Hematuria in a Large Chinese Family.
Cytogenet Genome Res;
154(3): 132-136, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29742505
5.
Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes.
Cytogenet Genome Res;
154(1): 30-36, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29669314
6.
Long-term outcome of mycophenolate mofetil treatment for patients with microscopic polyangiitis: an observational study in Chinese patients.
Rheumatol Int;
36(7): 967-74, 2016 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-27169414
7.
Kidney Organoid Modeling of WT1 Mutations Reveals Key Regulatory Paths Underlying Podocyte Development.
Adv Sci (Weinh);
: e2308556, 2024 May 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-38810140
8.
Pathogenic Gene Spectrum and Clinical Implication in Chinese Patients with Lupus Nephritis.
Clin J Am Soc Nephrol;
2023 Apr 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-37099456
9.
Establishment of the induced pluripotent stem cell line (NCKDi005-A) from a male patient with Alport syndrome carrying a homozygous frameshift mutation in the COL4A4 gene.
Stem Cell Res;
58: 102628, 2022 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34942480
10.
Next-Generation Sequencing-Based Genetic Diagnostic Strategies of Inherited Kidney Diseases.
Kidney Dis (Basel);
7(6): 425-437, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34901190
11.
Generation of the induced pluripotent stem cell line (NCKDi004-A) from a 17-year-old patient with Alport syndrome carrying a homozygous mutation in COL4A3 gene.
Stem Cell Res;
56: 102557, 2021 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34626894
12.
Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene.
Stem Cell Res;
53: 102293, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33780729
13.
Nocardiosis in patients with nephrotic syndrome: a retrospective analysis of 11 cases and a literature review.
Int Urol Nephrol;
52(4): 731-738, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-32124233
14.
A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome.
Kidney Dis (Basel);
6(1): 43-49, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-32021873
15.
Generation of induced pluripotent stem cell line (NCKDi001-A) from a 19-year-old patient with a novel COL4A5 gene mutation in Alport syndrome.
Stem Cell Res;
49: 102023, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33128955
16.
Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutation: A Two-Case Report and Literature Review.
Nephron;
143(4): 282-287, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31422399
17.
A Case of Switch from C3 Glomerulonephritis to Proliferative Glomerulonephritis with Monoclonal IgG Deposits.
Ann Clin Lab Sci;
48(4): 528-533, 2018 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-30143498
18.
Risk Factors for Renal Survival in Chinese Patients with Myeloperoxidase-ANCA-Associated GN.
Clin J Am Soc Nephrol;
12(3): 417-425, 2017 Mar 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28148558
19.
Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome.
PLoS One;
12(5): e0177685, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28542346
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