Ask about this productRelated genes to: SIPA1L2 antibody
- Gene:
- SIPA1L2 NIH gene
- Name:
- signal induced proliferation associated 1 like 2
- Previous symbol:
- -
- Synonyms:
- KIAA1389, SPAR2
- Chromosome:
- 1q42.2
- Locus Type:
- gene with protein product
- Date approved:
- 2003-12-11
- Date modifiied:
- 2019-04-09
Related products to: SIPA1L2 antibody
Related articles to: SIPA1L2 antibody
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Publication date: 2026/07/08
Somerville Emma NLiu LangTa MichaelIwaki HirotakaSenkevich KonstantinAlcalay Roy NGan-Or Ziv - Spinal cord injury (SCI) triggers a complex secondary injury cascade that critically limits neural repair. Although microRNAs have been implicated in post-SCI inflammation and neural regeneration, the key competing endogenous RNA (ceRNA) network regulating immune dysregulation remains unclear. - Source: PubMed
Publication date: 2026/05/07
Yao YuxuanGuo WenliangCai XingyunGui YuchangYao JingzhiLu YutingLiang YuxinWang WenshuTan ZhibiaoZhang JinxiangXu Jianwen - α-synucleinopathies are clinically and biologically heterogeneous disorders lacking reliable biomarkers to assist with early diagnosis, disease progression, patient stratification, and therapeutic targeting. Genetic variation is known to impact biomarker levels, influencing their utility and interpretation in research and clinical settings. We aimed to identify common genetic modulators of biomarker levels implicated in α-synucleinopathy pathogenesis. - Source: PubMed
Publication date: 2025/12/30
Somerville Emma NLiu LangTa MichaelIwaki HirotakaSenkevich KonstantinAlcalay Roy NGan-Or Ziv - Striae gravidarum (SG), commonly known as stretch marks, are a frequent connective tissue alteration observed in pregnant women. The presence of SG can negatively impact postpartum women's self-perception, potentially resulting in diminished self-esteem and psychological issues, including anxiety and depression. The study aimed to evaluate the potential risk factors and genetic associations of SG within a Chinese Han population. - Source: PubMed
Publication date: 2025/10/13
Xiong LidanYang LifengHe HailunChen JianguoWang YinshuDong XiujuLi LiHan Yuanyan - Alzheimer's disease (AD) continues to be the sixth leading cause of death in the United States. Significant efforts are spent researching etiology and potential management strategies. Although minorities face a higher disease burden and are anticipated to make up 43% of the US population by 2060, most literature on inherited AD risk has been derived from studying European ancestry. Here we evaluate frequencies of top AD risk alleles for late-onset AD (LOAD) in African- (AA), Mexican- (MA) and non-Hispanic White (NHW)-American participants enrolled in the Health & Aging Brain Study-Health Disparities (HABS-HD) cohort to determine ethnicity-specific differential genetic architecture. - Source: PubMed
Publication date: 2025/06/19
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