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Profil bibliographique

Linlin Li

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

20Publications signalées
219Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Genetic Associations and EpidemiologyPhotonic and Optical DevicesWnt/β-catenin signaling in development and cancerSemiconductor Lasers and Optical DevicesGenetics and Neurodevelopmental Disorders

Les publications récentes

Accès ouvert 2025 article OpenAlex

Concurrent anti-glomerular basement membrane disease and membranous nephropathy: a case report

Linlin Li, Panxin Niu, Na Li, Xiaoling Zhang et autres

Anti-glomerular basement membrane (GBM) disease is a rapidly progressive glomerulonephritis which, in rare instances, occurs concurrently with membranous nephropathy (MN). We report a case of this patient presented with proteinuria and hematuria, the predominant pathology was crescentic and necrotizing glomerulonephritis with linear …

cn (code pays fourni par la source)

0 citations Frontiers in Medicine
Accès ouvert 2025 article OpenAlex

Protocol for the quantitative detection of mtDNA in the supernatants of activated human naive CD8+ T cells

Linlin Li, Jun Jin

Here, we present a protocol for the quantitative characterization of human T cell aging. We describe steps for sample collection; peripheral blood mononuclear cell (PBMC) isolation; and the enrichment, assessment, and activation of naive CD8 + T cells. We then detail procedures …

cn (code pays fourni par la source)

0 citations STAR Protocols
Accès ouvert 2022 article OpenAlex

The first complete genome sequence and pathogenicity characterization of fowl adenovirus serotype 2 with inclusion body hepatitis and hydropericardium in China

Zimin Xie, Junqin Zhang, Minhua Sun, Qinghang Zeng et autres

Since 2015, fowl adenovirus (FAdV) has been frequently reported worldwide, causing serious economic losses to the poultry industry. In this study, a FAdV-2, namely GX01, was isolated from liver samples of chickens with hepatitis and hydropericardium in Guangxi Province, China. The complete …

cn (code pays fourni par la source)

8 citations Frontiers in Veterinary Science
Accès ouvert 2020 article OpenAlex

Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature

Linlin Li, Xinyue Zhang, Qingyang Shi, Leilei Li et autres

BACKGROUND: Trisomy of the short arm of chromosome 17 is a rare genomic disorder. The clinical features of complete trisomy 17p syndrome have been described. Most cases of this syndrome have been found in infants and children, but only a few cases …

cn (code pays fourni par la source)

4 citations Journal of Clinical Laboratory Analysis
Accès ouvert 2019 article OpenAlex

Obstetric and perinatal outcomes of intracytoplasmic sperm injection for infertile men with Y chromosome microdeletions

Qi Xi, Zhihong Zhang, Ruixue Wang, Linlin Li et autres

BACKGROUND: To evaluate the safety of intracytoplasmic sperm injection (ICSI) for men with Y chromosome azoospermia factor (AZF) microdeletions. METHODS: Twenty-five men with Y chromosome microdeletions and their partners underwent ICSI treatment. These subjects were matched against 50 ICSI cycles in which …

cn (code pays fourni par la source)

22 citations Medicine
Accès ouvert 2019 article OpenAlex

The reproductive outcome of an infertile man with AZFc microdeletions, via intracytoplasmic sperm injection in a high-risk pregnancy

Cong Hu, Xiangyin Liu, Linlin Li, Xiaonan Hu et autres

RATIONALE: Infertile men with Y-chromosome microdeletions have been reported to be able to have their own children via intracytoplasmic sperm injection (ICSI). PATIENT CONCERNS: A 27-year-old man with Y-chromosome azoospermia factor c (AZFc) deletions underwent ICSI treatment. The pregnancy showed a high …

cn (code pays fourni par la source)

4 citations Medicine
Accès ouvert 2015 article OpenAlex

Association of Canonical Wnt/β-Catenin Pathway and Type 2 Diabetes: Genetic Epidemiological Study in Han Chinese

Jinjin Wang, Jingzhi Zhao, Jianfeng Zhang, Xinping Luo et autres

We aimed to investigate the associations of polymorphisms in Canonical Wnt/β-catenin pathway (WNT) signaling genes (including low-density lipoprotein-related protein 5 [LRP5] and transcription factor 7-like 2 [TCF7L2] gene) and the downstream gene glucagon (GCG) and risk of type 2 diabetes mellitus (T2DM) …

cn (code pays fourni par la source)

15 citations Nutrients

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