Zobrazeno 1 - 10
of 82
pro vyhledávání: '"L. Malki"'
Publikováno v:
All Days.
Abstract Low primary recovery percentages (usually 10% or less) in unconventional reservoirs, such as the Three Forks Formation in the Williston Basin, mean that potentially billions of barrels of oil are left behind in the reservoirs. Gas enhanced o
Publikováno v:
All Days.
Abstract An in-depth description of the objectives of rich gas cyclic huff 'n' puff in the Three Forks of the Williston Basin, as well as the design, field operations, production, pressure, and other surveillance results, is provided in this case stu
Publikováno v:
All Days.
ABSTRACT: The primary oil recovery in the Bakken Petroleum System is still small, with a range of 5% to 12% of the original oil in place (OOIP). This study aims to investigate the potential and the performance of CO2 injection with HnP on the recover
Publikováno v:
All Days.
ABSTRACT: The Bakken Petroleum System in the Williston Basin consists of three main members: Upper Bakken Shale (UB), Middle Bakken (MB), and Lower Bakken Shale (LB). The Middle Bakken is a calcareous siltstone and fine-grained sandstone which is a p
Autor:
Sari Assaf, K. Malovitski, Alon Peled, L. Malki, Eli Sprecher, M. Pavlovsky, T. Mayer, Dan Vodo, Ofer Sarig, J. Mohamad
Publikováno v:
British Journal of Dermatology. 184:1153-1160
Background Pemphigus vulgaris (PV) is a life-threatening mucocutaneous autoimmune blistering disease. We previously showed that genetic variants within the ST18 gene promoter area confer a sixfold increase in the propensity to develop PV. ST18, a tra
Autor:
A. Peled, Eli Sprecher, Miguel Weil, R. Bochner, M. Pavlovsky, L. Malki, Liat Samuelov, Edward Pichinuk, Ofer Sarig
Publikováno v:
British Journal of Dermatology. 183:114-120
BACKGROUND Hypotrichosis simplex of the scalp (HSS) is characterized by progressive loss of scalp hair that results in almost complete baldness at a young age. HSS is often caused by dominant nonsense mutations in CDSN encoding corneodesmosin, leadin
Autor:
J. Mohamad, L. Samuelov, S. Assaf, L. Malki, K. Malovitski, N. Adir, E. Granot, M. Pavlovsky, O. Sarig, E. Sprecher
Publikováno v:
Journal of Investigative Dermatology. 142:S227
Autor:
M. Eskin-Schwartz, Eran Cohen-Barak, Ora Bitterman-Deutsch, Sari Assaf, John A. McGrath, Stavit A. Shalev, N. Malchin, Noam Shomron, Giles G. Lestringant, Gideon Bach, Kiril Malovitski, Jacob Mashiah, Vered Molho-Pessach, Eli Sprecher, Tom Rabinowitz, L. Malki, Shirli Israeli, Ben Zion Garty, Arti Nanda, J. Mohamad, Avikam Harel, Liat Samuelov, Ofer Sarig, Meital Grafi-Cohen, Reuven Bergman
Publikováno v:
Experimental dermatologyREFERENCES. 30(9)
Autosomal recessive congenital ichthyosis (ARCI) is a rare and heterogeneous skin cornification disorder presenting with generalized scaling and varying degrees of erythema. Clinical manifestations range from lamellar ichthyosis (LI), congenital icht
Autor:
Sari Assaf, Talia Canter, Arti Nanda, Kiril Malovitski, Eli Sprecher, Nicole Cesarato, Yossi Anis, Liat Samuelov, Bethany E. Perez White, Dan Vodo, Regina C. Betz, J. Mohamad, Holger Thiele, Andrea Gat, Amy S. Paller, M. Pavlovsky, Ofer Bihari, L. Malki, Ofer Sarig
Publikováno v:
Genet Med
PURPOSE: Localized autosomal recessive hypotrichosis (LAH) has been associated with pathogenic variants in DSG4, encoding a desmosomal protein as well as in LIPH and LPAR6, encoding respectively lipase H, which catalyzes the formation of 2-acyl-lysop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9538a579fc561f5b84f567136c3adc2d
https://europepmc.org/articles/PMC7405639/
https://europepmc.org/articles/PMC7405639/
Autor:
Ofer Sarig, M. Pavlovsky, Alon Peled, Kiril Malovitski, Eli Sprecher, Shahar Taiber, Tom Rabinowitz, Noam Shomron, J. Mohamad, Liat Samuelov, Noam Adir, Gilles G. Lestringant, Joshua D. Milner, L. Malki
Publikováno v:
Clinical and experimental dermatologyReferences. 46(1)
Background Palmoplantar keratoderma (PPK) refers to a large group of disorders characterized by extensive genetic and phenotypic heterogeneity. PPK diagnosis therefore increasingly relies upon genetic analysis. Aim To delineate the genetic defect und