Pages that link to "Q28265922"
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The following pages link to Presenilin mutations in Alzheimer's disease (Q28265922):
Displaying 50 items.
- A myristoylated calcium-binding protein that preferentially interacts with the Alzheimer's disease presenilin 2 protein (Q22009982) (← links)
- The Accurate Diagnosis of Early-Onset Dementia (Q22241314) (← links)
- Substitution of a glycogen synthase kinase-3beta phosphorylation site in presenilin 1 separates presenilin function from beta-catenin signaling (Q24290586) (← links)
- Hydrocephalus and abnormal subcommissural organ in mice lacking presenilin-1 in Wnt1 cell lineages (Q24617724) (← links)
- Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease (Q24646877) (← links)
- Using animal models to determine the significance of complement activation in Alzheimer's disease (Q24796236) (← links)
- Overview of Alzheimer's Disease and Some Therapeutic Approaches Targeting Aβ by Using Several Synthetic and Herbal Compounds (Q26749061) (← links)
- The genetic landscape of Alzheimer disease: clinical implications and perspectives (Q26796582) (← links)
- Direct interaction of Alzheimer's disease-related presenilin 1 with armadillo protein p0071 (Q28139646) (← links)
- NBR1 interacts with fasciculation and elongation protein zeta-1 (FEZ1) and calcium and integrin binding protein (CIB) and shows developmentally restricted expression in the neural tube (Q28202584) (← links)
- Interaction with telencephalin and the amyloid precursor protein predicts a ring structure for presenilins (Q28206918) (← links)
- Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene (Q28280248) (← links)
- Presenilin 1 is essential for cardiac morphogenesis (Q28592290) (← links)
- Identification of caspases that cleave presenilin-1 and presenilin-2 (Q29999194) (← links)
- Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2. (Q30493972) (← links)
- COMUS: Clinician-Oriented locus-specific MUtation detection and deposition System (Q30951177) (← links)
- Involvement of cell cycle elements, cyclin-dependent kinases, pRb, and E2F x DP, in B-amyloid-induced neuronal death (Q33178580) (← links)
- Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40. (Q33245678) (← links)
- Notch and the immune system. (Q33812251) (← links)
- YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14. (Q33856418) (← links)
- Current status on Alzheimer disease molecular genetics: from past, to present, to future (Q33871345) (← links)
- Detailed characterization of neuroprotection by a rescue factor humanin against various Alzheimer's disease-relevant insults. (Q33956027) (← links)
- Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample (Q34114558) (← links)
- Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian population. (Q34145734) (← links)
- Disease-related mutations among Caribbean Hispanics with familial dementia (Q34311130) (← links)
- Mitochondrial genomic analysis of late onset Alzheimer's disease reveals protective haplogroups H6A1A/H6A1B: the Cache County Study on Memory in Aging (Q34428180) (← links)
- Ethical principles and pitfalls of genetic testing for dementia (Q34496182) (← links)
- Aberrant subcellular neuronal calcium regulation in aging and Alzheimer's disease (Q34547754) (← links)
- Genetics of Alzheimer's disease: a centennial review (Q34656812) (← links)
- Pharmacogenomics for the treatment of dementia (Q35009345) (← links)
- Structural and mechanistic commonalities of amyloid-β and the prion protein (Q35578753) (← links)
- Amyloid deposition begins in the striatum of presenilin-1 mutation carriers from two unrelated pedigrees (Q35694218) (← links)
- Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors (Q35889850) (← links)
- A notable cleavage: winding up with beta-amyloid (Q35962502) (← links)
- Restricted growth and insulin-like growth factor-1 deficiency in mice lacking presenilin-1 in the neural crest cell lineage (Q36182427) (← links)
- Locus-specific mutation databases for neurodegenerative brain diseases (Q36302037) (← links)
- Genetics, transcriptomics, and proteomics of Alzheimer's disease (Q36466472) (← links)
- Redox proteomics in some age-related neurodegenerative disorders or models thereof (Q36525171) (← links)
- C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic (Q36576421) (← links)
- Frontotemporal dementia-like phenotypes associated with presenilin-1 mutations (Q36583604) (← links)
- Alternative Splicing in Alzheimer's Disease (Q36635086) (← links)
- Reassessing the amyloid cascade hypothesis of Alzheimer's disease (Q37187966) (← links)
- Familial Alzheimer's disease mutations in presenilins: effects on endoplasmic reticulum calcium homeostasis and correlation with clinical phenotypes (Q37201294) (← links)
- Molecular genetics of Alzheimer's disease: an update (Q37209771) (← links)
- gamma-secretases: from cell biology to therapeutic strategies (Q37686625) (← links)
- Presenilins function in ER calcium leak and Alzheimer's disease pathogenesis (Q37887931) (← links)
- Presenilins as endoplasmic reticulum calcium leak channels and Alzheimer's disease pathogenesis (Q37904894) (← links)
- Neuroinflammation in Alzheimer's disease: from pathogenesis to a therapeutic target (Q38202910) (← links)
- Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment. (Q40242218) (← links)
- Presenilin-1 is an unprimed glycogen synthase kinase-3beta substrate (Q40260863) (← links)