Pages that link to "Q22009038"
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The following pages link to Mutations in ATP2A2, encoding a Ca2 pump, cause Darier disease (Q22009038):
Displaying 50 items.
- Initial sequencing and analysis of the human genome (Q21045365) (← links)
- ATPase sarcoplasmic/endoplasmic reticulum Ca2 transporting 2 (Q21115319) (← links)
- PFM1 (PRDM4), a new member of the PR-domain family, maps to a tumor suppressor locus on human chromosome 12q23-q24.1 (Q22010757) (← links)
- Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease (Q22010996) (← links)
- Pemphigus vulgaris antibody identifies pemphaxin. A novel keratinocyte annexin-like molecule binding acetylcholine (Q22254621) (← links)
- SERCA1 truncated proteins unable to pump calcium reduce the endoplasmic reticulum calcium concentration and induce apoptosis (Q24291323) (← links)
- Human keratinocyte ATP2C1 localizes to the Golgi and controls Golgi Ca2 stores (Q24300260) (← links)
- Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356 (Q24305186) (← links)
- DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24. (Q24535597) (← links)
- How do keratinizing disorders and blistering disorders overlap? (Q27004098) (← links)
- Chamber Specific Gene Expression Landscape of the Zebrafish Heart (Q27324640) (← links)
- TRP Channels in Skin Biology and Pathophysiology (Q28066420) (← links)
- Jagged-1 mutation analysis in Italian Alagille syndrome patients (Q28146037) (← links)
- Desmosomal cadherins (Q28201843) (← links)
- Mutations of either or both Cys876 and Cys888 residues of sarcoplasmic reticulum Ca2 -ATPase result in a complete loss of Ca2 transport activity without a loss of Ca2 -dependent ATPase activity. Role of the CYS876-CYS888 disulfide bond (Q28204694) (← links)
- Are desmosomes more than tethers for intermediate filaments? (Q28205062) (← links)
- Three novel sarco/endoplasmic reticulum Ca2 -ATPase (SERCA) 3 isoforms. Expression, regulation, and function of the membranes of the SERCA3 family (Q28214899) (← links)
- Mutation analysis of ATP2C1 gene in Taiwanese patients with Hailey-Hailey disease (Q28215360) (← links)
- Identification, expression, function, and localization of a novel (sixth) isoform of the human sarco/endoplasmic reticulum Ca2 ATPase 3 gene (Q28251173) (← links)
- Plasticity and adaptation of Ca2 signaling and Ca2 -dependent exocytosis in SERCA2( /-) mice. (Q28366127) (← links)
- Gene knockout studies of Ca2 -transporting ATPases (Q28863817) (← links)
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization (Q28654771) (← links)
- Intracellular Ca2 signaling and store-operated Ca2 entry are required in Drosophila neurons for flight (Q30488393) (← links)
- Upregulation of P-cadherin expression in the lesional skin of pemphigus, Hailey-Hailey disease and Darier's disease (Q30991876) (← links)
- Immunohistological study of involucrin expression in Darier's disease skin (Q33321933) (← links)
- Management of Darier's disease (Q33610971) (← links)
- The coexistence of Darier's disease and Hailey-Hailey disease symptoms (Q33645898) (← links)
- Endoplasmic reticulum calcium pumps and cancer cell differentiation (Q33649613) (← links)
- Genetics of bipolar disorder. (Q33721526) (← links)
- Mapping complex traits in diseases of the hair and skin (Q33793837) (← links)
- Cutaneous gene therapy. Principles and prospects (Q33811552) (← links)
- A novel genodermatosis caused by mutations in plakophilin 1, a structural component of desmosomes. (Q33817907) (← links)
- Endoplasmic reticulum calcium, stress, and cell-to-cell adhesion (Q33851720) (← links)
- Spectrum of novel ATP2A2 mutations in patients with Darier's disease. (Q33870392) (← links)
- Parallel adaptive divergence among geographically diverse human populations (Q33940765) (← links)
- Human skeletal muscle fibres: molecular and functional diversity (Q34013694) (← links)
- Acantholytic dyskeratotic acanthoma: case report and review of the literature (Q34041601) (← links)
- Recent advances in the molecular basis of inherited skin diseases (Q34063956) (← links)
- Genetics of bipolar affective disorder (Q34108344) (← links)
- SERCaMP: a carboxy-terminal protein modification that enables monitoring of ER calcium homeostasis (Q34166885) (← links)
- Sarco(endo)plasmic reticulum calcium pumps: recent advances in our understanding of structure/function and biology (review). (Q34219003) (← links)
- Gene mutations, great expectations (Q34258806) (← links)
- Searching for candidate genes in the new millennium. (Q34291344) (← links)
- Keratinocyte adhesion and the missing link: from Dowling-Meara to Hay-Wells. St John's Hospital Dermatological Society Annual Oration 2000. (Q34291351) (← links)
- Desmosomes: structure and function in normal and diseased epidermis (Q34321018) (← links)
- The genetics of human skin disease (Q34355367) (← links)
- Desmosome assembly and dynamics (Q34360181) (← links)
- Molecular genetics of Ca(2 ) stores and intracellular Ca(2 ) signalling. (Q34360409) (← links)
- Darier's (Darier-White) disease/keratosis follicularis (Q34408530) (← links)
- Endoplasmic reticulum Ca2 depletion activates XBP1 and controls terminal differentiation in keratinocytes and epidermis (Q34440575) (← links)