Mate and fuse: how yeast cells do it
Many cells are able to orient themselves in a non-uniform environment by responding to
localized cues. This leads to a polarized cellular response, where the cell can either grow or …
localized cues. This leads to a polarized cellular response, where the cell can either grow or …
Central sensitization in chronic low back pain: a narrative review
I Sanzarello, L Merlini, MA Rosa… - Journal of back and …, 2016 - content.iospress.com
Low back pain is one of the four most common disorders in all regions, and the greatest
contributor to disability worldwide, adding 10.7% of total years lost due to this health state. The …
contributor to disability worldwide, adding 10.7% of total years lost due to this health state. The …
[HTML][HTML] Orbital tumours and tumour-like lesions: exploring the armamentarium of multiparametric imaging
Although the orbit is a small anatomical space, the wide range of structures present within it
are often the site of origin of various tumours and tumour-like conditions, both in adults and …
are often the site of origin of various tumours and tumour-like conditions, both in adults and …
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
…, S Varnous, HM Bécane, EH Hammouda, L Merlini… - Nature …, 1999 - nature.com
Emery-Dreifuss muscular dystrophy (EDMD) is characterized by early contractures of
elbows and Achilles tendons, slowly progressive muscle wasting and weakness, and a …
elbows and Achilles tendons, slowly progressive muscle wasting and weakness, and a …
Clinical and molecular genetic spectrum of autosomal dominant Emery‐Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
…, HM Becane, D Recan, L Merlini… - Annals of Neurology …, 2000 - Wiley Online Library
Emery‐Dreifuss muscular dystrophy (EDMD) is characterized by early contractures of the
elbows and Achilles tendons, slowly progressive muscle wasting and weakness, and life‐…
elbows and Achilles tendons, slowly progressive muscle wasting and weakness, and life‐…
[PDF][PDF] Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome
…, B Van der Zwaag, H Kayserili, L Merlini… - The American Journal of …, 2002 - cell.com
Walker-Warburg syndrome (WWS) is an autosomal recessive developmental disorder
characterized by congenital muscular dystrophy and complex brain and eye abnormalities. A …
characterized by congenital muscular dystrophy and complex brain and eye abnormalities. A …
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
…, B Blaauw, A Urciuolo, T Tiepolo, L Merlini… - Nature medicine, 2010 - nature.com
… find any substantial difference between wild-type and Col6a1 −/− muscles in the protein
amounts of B cell leukemia/lymphoma-2 (Bcl-2), Bcl-2–associated X protein (Bax) and Bcl-X L …
amounts of B cell leukemia/lymphoma-2 (Bcl-2), Bcl-2–associated X protein (Bax) and Bcl-X L …
[PDF][PDF] Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C
Mandibuloacral dysplasia (MAD) is a rare autosomal recessive disorder, characterized by
postnatal growth retardation, craniofacial anomalies, skeletal malformations, and mottled …
postnatal growth retardation, craniofacial anomalies, skeletal malformations, and mottled …
[PDF][PDF] Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy (EMD) is a condition characterized by the clinical triad
of early-onset contractures, progressive weakness in humeroperoneal muscles, and …
of early-onset contractures, progressive weakness in humeroperoneal muscles, and …
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α …
The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal
recessive disorders. A new pathomechanism has recently been identified in a group of these …
recessive disorders. A new pathomechanism has recently been identified in a group of these …