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Gonzalo Blanco
Observed names:
Blanco, G,
Blanco, Gonzalo,
Dr. Gonzalo Blanco,
G Blanco,
G. Blanco
Institution:
University of York
Observed institutions:
Universitat Autònoma de Barcelona,
University of Sussex,
Mary Lyon Centre at MRC Harwell,
St Mary's Hospital,
University of York,
Universidad de Sevilla
show all 6
ORCID:
0000-0003-3827-3111
Observed ORCID:
0000-0003-3827-3111
OpenAlex ID:
A5032364434
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1
2021
·
Daniel J. Klionsky
, Amal Kamal Abdel-Aziz
, et al.
·
Autophagy
·
2,608
PDF
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
2003
·
Philomena Mburu
, Mirna Mustapha
, et al.
·
Nature Genetics
·
345
Excretion of ammonium by a nifL mutant of Azotobacter vinelandii fixing nitrogen
1992
·
A Bali
, G Blanco
, et al.
·
Applied and Environmental Microbiology
·
153
PDF
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
2021
·
Klionsky, Daniel J
, Abdel-Aziz, Amal Kamal
, et al.
·
Research at the University of Copenhagen (University of Copenhagen)
·
104
The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific protein
2001
·
G. Blanco
·
Human Molecular Genetics
·
96
Sequence and molecular analysis of the nifL gene of Azotobacter vinelandii
1993
·
Gonzalo Blanco
, Martin Drummond
, et al.
·
Molecular Microbiology
·
91
The product of the nitrogen fixation regulatory gene nfrX of Azotobacter vinelandii is functionally and structurally homologous to the uridylyltransferase encoded by glnD in enteric bacteria
1991
·
A Contreras
, M Drummond
, et al.
·
Journal of Bacteriology
·
63
Filamin C interacts with the muscular dystrophy KY protein and is abnormally distributed in mouse KY deficient muscle fibres
2004
·
Jane Beatham
, Rosario Romero
, et al.
·
Human Molecular Genetics
·
46
PDF
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion
2016
·
Nasim Vasli
, Elizabeth Harris
, et al.
·
Brain
·
41
Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1
2010
·
Jane Baker
, Genna Riley
, et al.
·
Experimental Cell Research
·
38
Disrupted autophagy undermines skeletal muscle adaptation and integrity
2016
·
Elliot J. Jokl
, Gonzalo Blanco
·
Mammalian Genome
·
37
PDF
ZAKβ is activated by cellular compression and mediates contraction‐induced MAP kinase signaling in skeletal muscle
2022
·
Cathrine Nordgaard
, Anna Constance Vind
, et al.
·
The EMBO Journal
·
34
PDF
Identification of an operon involved in the assimilatory nitrate‐reducing system of Azotobacter vineiandii
1993
·
Francisco Ramos
, Gonzalo Blanco
, et al.
·
Molecular Microbiology
·
34
Refined Mapping of the Usher Syndrome Type III Locus on Chromosome 3, Exclusion of Candidate Genes, and Identification of the Putative Mouse Homologous Region
1996
·
Tarja Joensuu
, Gonzalo Blanco
, et al.
·
Genomics
·
32
IGFN1_v1 is required for myoblast fusion and differentiation
2017
·
Xiang Li
, Jane Baker
, et al.
·
PLoS ONE
·
30
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis
2014
·
Silvia Corrochano
, Roope Männikkö
, et al.
·
Brain
·
29
PDF
Candidate testis‐determining gene, Maestro (Mro), encodes a novel HEAT repeat protein
2003
·
Lee Smith
, Nick Van Hateren
, et al.
·
Developmental Dynamics
·
25
PDF
Proteomic analysis of laser capture microscopy purified myotendinous junction regions from muscle sections
2014
·
Tugba Can
, Laura Faas
, et al.
·
Proteome Science
·
20
PDF
Reaching and grasping phenotypes in the mouse (Mus musculus): A characterization of inbred strains and mutant lines
2007
·
V. Tucci
, F. Achilli
, et al.
·
Neuroscience
·
20
Proteomic resolution of IGFN1 complexes reveals a functional interaction with the actin nucleating protein COBL
2020
·
Tobias Cracknell
, Steinar Mannsverk
, et al.
·
Experimental Cell Research
·
19
Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse
2009
·
Francesca E. Mackenzie
, Rosario Romero
, et al.
·
Human Molecular Genetics
·
19
PDF
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease
2018
·
Silvia Corrochano
, Gonzalo Blanco
, et al.
·
Human Molecular Genetics
·
18
PDF
A Nonsense Mutation in Mouse Tardbp Affects TDP43 Alternative Splicing Activity and Causes Limb-Clasping and Body Tone Defects
2014
·
Thomas Ricketts
, Philip McGoldrick
, et al.
·
PLoS ONE
·
18
PDF
Determination of Muscle Fiber Type in Rodents
2012
·
Bernadett Kalmar
, Gonzalo Blanco
, et al.
·
Current Protocols in Mouse Biology
·
16
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb
2011
·
Ramakrishna Kurapati
, Caoimhe McKenna
, et al.
·
Human Molecular Genetics
·
16
PDF
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Works count:
54
Citation count:
4,056
H-index:
19
I10-index:
30
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