Results 141 to 150 of about 3,789 (186)

TLNRD1 is a CCM complex component and regulates endothelial barrier integrity. [PDF]

J Cell Biol
Ball NJ, Ghimire S, Follain G, Pajari AO, Wurzinger D, Vaitkevičiūtė M, Cowell AR, Berki B, Ivaska J, Paatero I, Goult BT, Jacquemet G.   +11 more
europepmc   +1 more source

Natural history of familial cerebral cavernous malformations: the CCM_Italia cohort study. [PDF]

Front Neurol
Lanfranconi S, Scola E, Novelli D, Poggesi A, Pescini F, Pavanello M, Romano F, D'Alessandris QG, Marani W, Signorelli F, Iaconetta G, Torelli G, Fainardi E, Severino M, Remore LG, Bertani GA, Conte G, Capra V, Vasamì A, Nicolis E, Contino G, Ronchi D, Palmieri MC, Previtali A, Mattogno PP, Sturiale CL, Solarino ME, Caliulo R, Bozzi MT, Fratini F, Zanier ER, Latini R, Meessen JMTA, Locatelli M, and the CCM_Italia investigators.   +34 more
europepmc   +1 more source

Familial Cerebral Cavernous Malformations : A Clinical Series and Literature Review. [PDF]

J Korean Neurosurg Soc
Dogu H, Mucuoglu AO, Gokoglu A, Gasimli R, Tepeli E, Akdemir H.   +5 more
europepmc   +1 more source

Fare meme kanseri modeli primer tümör ve metastazlarında CCM1, CCM2, CCM3 ekspresyonlarının değerlendirilmesi

, 2017
Amaç: CCM1, CCM2 ve CCM3 genlerinde tanımlanan mutasyonlar sporadik ya da kalıtsal olup santral sinir sisteminde görülen serebral kavernoz malformasyonların (SKM) sebebidir. Bu genlerin fonksiyonları hala tam olarak anlaşılamamasına rağmen; hücre-hücre bağlantılarında, migrasyonda, hücrenin oryantasyonunda ve apoptozunda önemli rollerinin olduğu ...
openaire   +2 more sources

Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. [PDF]

Eur J Hum Genet
Chaussenot A, Ayrignac X, Chatron N, Granchon-Riolzir T, Labauge P, Tournier-Lasserve E, Riant F.   +6 more
europepmc   +1 more source

Guidelines for the Diagnosis and Clinical Management of Cavernous Malformations of the Brain and Spinal Cord: Consensus Recommendations Based on a Systematic Literature Review by the Alliance to Cure Cavernous Malformation Clinical Advisory Board Experts Panel. [PDF]

Neurosurgery
Akers AL, Albanese J, Alcazar-Felix RJ, Al-Shahi Salman R, Awad IA, Connolly ES, Danehy A, Flemming KD, Gordon E, Hage S, Kim H, Lanzino G, Lee CH, McCormick PC, Mabray MC, Marchuk DA, Smith E, Smith KM, Srivastava S, Taylor JM, Vadivelu S.   +20 more
europepmc   +1 more source

A novel mutation associated with multiple cerebral and vertebral cavernous malformations [PDF]

core   +1 more source

Quantifying the effects of exceptional fossil preservation on the global availability of phylogenetic data in deep time. [PDF]

PLoS One
Woolley CH, Bottjer DJ, Corsetti FA, Smith ND.   +3 more
europepmc   +1 more source

Plasma cell-free DNA methylation profile before afatinib treatment is associated with progression-free and overall survival of patients with epidermal growth factor receptor gene mutation-positive non-small cell lung cancer. [PDF]

Clin Epigenetics
Fujimoto M, Yasuda H, Arai E, Nakajima M, Takata S, Morikawa K, Tanaka H, Itani H, Honda T, Horiuchi K, Watanabe K, Nakagawa H, Nakahara Y, Seki Y, Bessho A, Takahashi N, Hayashi K, Endo T, Takeyama K, Maekura T, Takigawa N, Kawase A, Endoh M, Nemoto K, Kishi K, Soejima K, Okuma Y, Togashi A, Matsutani N, Seki N, Kanai Y.   +30 more
europepmc   +1 more source

CCM Function in the Heart: Working From Outside-In Rather Than Inside-Out. [PDF]

JACC Basic Transl Sci
Kahn ML.
europepmc   +1 more source