Opposing Pressures of Speed and Efficiency Guide the Evolution of Molecular Machines. [PDF]
Many biomolecular machines need to be both fast and efficient. How has evolution optimized these machines along the tradeoff between speed and efficiency?
Dill, Ken, Wagoner, Jason
core
Molecular structure and developmental expression of zebrafish atp2a genes [PDF]
[[abstract]]We isolated two atp2a genes, atp2a1 and atp2a2a, from embryonic zebrafish. Amino acid sequences deduced from zebrafish atp2a genes are aligned with orthologue proteins from other species, the results showed that they share high percentage of ...
A. Magyar +49 more
core +1 more source
Darier disease with oral and esophageal involvement: A case report
A 58-year-old man presented with itchy papular eruptions all over the body since 15 years. Intraoral examination revealed raised papular lesions on the labial mucosa, hard palate, and tongue.
Magesh Karuppur Thiagarajan +2 more
doaj +1 more source
A plazmamembrán Ca2+ ATPáz 4b izoforma apoptotikus fragmentjét reprezentáló mutáns sejten belüli lokalizációja, stabilitása, hatásai a sejtek Ca2+ háztartására és szerepe az apoptózis folyamatban = Intracellular localization and stability of a mutant representing the apoptotic fragment of the plasma membrane Ca2+ ATPase 4b and its role in cellular Ca2+ homeostasis and apoptosis [PDF]
A jelen kutatási periódus alatt egy fontos Ca2+ transzport fehérje, a plazma membrán Ca2+ ATPáz (PMCA4b) struktúra/funkció változásait tanulmányoztuk az apoptózis valamint a nekrózis folyamatai alatt. Eredményeink azt bizonyítják, hogy a PMCA4b fehérjét -
Antalffy, Géza +5 more
core
A case of segmental Darier disease treated with doxycycline monotherapy [PDF]
Cory Pettit +3 more
openalex +1 more source
Haemorrhagic Darier's Disease [PDF]
I H, Coulson, K J, Misch
openaire +2 more sources
Darier Disease: A Case Series of 20 Patients and Review of the Literature
E.M. Sánchez Martínez +3 more
openalex +1 more source
Fibropapilomatosis oral múltiple como manifestación inicial de Síndrome de Cowden: caso clínico [PDF]
El síndrome de Cowden es una infrecuente enfermedad hereditaria englobada dentro de las poliposis gastrointestinales de tipo hamartomatoso. Se caracteriza por asociar anomalías cutaneomucosas y por la extraordinaria tendencia a desarrollar neoplasias ...
Capitán Cañadas, L.M. +4 more
core +1 more source
SERCA2 Haploinsufficiency in a Mouse Model of Darier Disease Causes a Selective Predisposition to Heart Failure [PDF]
Vikram Prasad +7 more
openalex +1 more source

