Results 201 to 210 of about 4,207 (232)
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A 100-Yr CCM1 Simulation of North China's Hydrologic Cycle

Journal of Climate, 1996
Abstract The year to year variability in North China's summertime hydrologic cycle is analyzed in a 100-yr CCM1 simulation. Eastern North America is included for comparative purposes with earlier work. On the basis of the simulated inherent variability of the regionally averaged soil moisture, each year's climate pattern over these two regions is ...
Zengquan Fan, Robert J. Oglesby
openaire   +1 more source

Modifications and Enhancements to the NCAR Community Climate Model (CCM1)

1989
This report describes the two new unresequenced program libraries created for CCM1 in the early fall, 1988 which incorporate fixes to several bugs that were discovered earlier, improvements in computational performance, and a number of other enhancements to components of the model.
Hack, James   +3 more
openaire   +1 more source

A novel CCM1 gene mutation causes cerebral cavernous malformation in a Chinese family

Journal of Clinical Neuroscience, 2011
Familial cerebral cavernous malformations (CCMs) are characterized by an autosomal dominant transmission with incomplete penetrance. We have previously reported a 1292delAT mutation in the CCM1 gene in a Chinese family with CCM. Here we report a novel deletion of CCM1 that correlates strongly with CCM formation in another family.
Yao, Zhao   +10 more
openaire   +2 more sources

A novel KRIT1/CCM1 mutation accompanied by a NOTCH3 mutation in a Chinese family with multiple cerebral cavernous malformations

Neurogenetics, 2023
Chunwang Li   +10 more
semanticscholar   +1 more source

Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformation

Neurology, 2005
Cerebral cavernous malformations (CCMs) are heterogeneous vascular malformations that may cause headaches, seizures, focal neurologic deficits, stroke, and death. With an incidence of 0.1 to 0.5%, they constitute 10 to 20% of all CNS vascular malformations.1 Heterozygous loss-of-function mutations have been identified in KRIT1 ( CCM1 ),2 MGC4607 ( CCM2
M F, Waters   +4 more
openaire   +2 more sources

Neue CCM1-Mutation bei einem 2-Jährigen

Monatsschrift Kinderheilkunde, 2007
O. Sürücü   +6 more
openaire   +1 more source

Novel CCM1 (KRIT1) mutation detection in Brazilian familial Cerebral cavernous malformation: Different genetic variants in inflammation, oxidative stress and drug metabolism genes affect disease aggressiveness.

World Neurosurgery, 2020
F. Fontes-Dantas   +9 more
semanticscholar   +1 more source

[Analysis of CCM1 gene mutations in Chinese patients with intracranial cavernous malformations].

Zhonghua yi xue za zhi, 2007
To study the CCM1 gene (7q11.2 - q22) mutations in Chinese patients with intracranial cavernous malformations (ICM), METHODS: Peripheral blood samples were collected from 25 unrelated patients with ICM confirmed by post-operational pathology, 7 being with familial ICM, all of Han nationality, and from 30 healthy people as controls.
Rong, Xie   +5 more
openaire   +1 more source

Documentation of NCAR CCM1 Program Modules

1987
Bath, Linda   +4 more
openaire   +1 more source

First Report of Concomitant Pathogenic Mutations Within MGC4607/CCM2 and KRIT1/CCM1 in a Familiar Cerebral Cavernous Malformation Patient.

World Neurosurgery, 2020
Gustavo da Fontoura Galvão   +5 more
semanticscholar   +1 more source

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