Methods of permeabilization
G Banfalvi, G Banfalvi - Permeability of Biological Membranes, 2016 - Springer
Viable cells are capable of living, developing and reproducing themselves. Under
experimental conditions the parameters of viability are diverse and measured by different …
experimental conditions the parameters of viability are diverse and measured by different …
Possible evolutionary links between immunoglobulin light chains and other proteins involved in amyloidosis
FJ Stevens - Amyloid, 2008 - Taylor & Francis
With limited exceptions, proteins that account for the amyloidoses appear to be
evolutionarily unrelated. Transthyretin is classified as having an “immunoglobulin-like” fold …
evolutionarily unrelated. Transthyretin is classified as having an “immunoglobulin-like” fold …
Degradação de quitina em Chromobacterium: proposição da via catabólica e expressão heteróloga de uma monooxigenase lítica de polissacarídeo de C. violaceum …
MR Fernandes - 2017 - repositorio.ufc.br
RESUMO O gênero Chromobacterium é composto por Betaproteobactérias Gram-
negativas, saprofíticas e de vida livre, com alguns representantes patogênicos. O grupo …
negativas, saprofíticas e de vida livre, com alguns representantes patogênicos. O grupo …
Contributions of genetically-modified animal models to the understanding and intervention in autosomal dominant polycystic kidney disease: present and future
AG Amaral, EH Watanabe, LF Onuchic - Revista de Medicina, 2016 - revistas.usp.br
Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent monogenic
renal disease, representing the fourth cause of end-stage kidney disease. This disorder …
renal disease, representing the fourth cause of end-stage kidney disease. This disorder …
[PDF][PDF] The Role of Primary Cilia in the Pathogenesis of ADPKD
PP Prosseda - 2016 - etheses.whiterose.ac.uk
ABSTRACT Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common
inherited kidney disease. Mutations in PKD1 (85%) or PKD2 (15%) account for almost all …
inherited kidney disease. Mutations in PKD1 (85%) or PKD2 (15%) account for almost all …
A METABOLOMIC, STRUCTURAL AND FUNCTIONAL STUDY OF POLYCYSTIN1 AND NEPHROCYSTIN1
V Mannella - 2013 - air.unimi.it
Abstract Nephronophthisis (NPHP) and Autosomal Dominant Polycystic Kidney Disease
(ADPKD) are two genetic renal cystic diseases that lead to End Stage Renal Disease …
(ADPKD) are two genetic renal cystic diseases that lead to End Stage Renal Disease …
[图书][B] Investigating the mechanism of renal cystogenesis in tuberous sclerosis and polycystic kidney disease
CS Bonnet - 2009 - search.proquest.com
Tuberous sclerosis (TSC) is an autosomal dominant disorder caused by germline mutations
in either TSC1 or TSC2 and characterised by the development of benign hamartomatous …
in either TSC1 or TSC2 and characterised by the development of benign hamartomatous …