Laminin α2 chain‐null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)‐deficient congenital muscular dystrophy [PDF]
Yuko Miyagoe +7 more
openalex +1 more source
Merosin-deficient congenital muscular dystrophy type 1A: A case report
Zhanwen He +5 more
openalex +2 more sources
Laminin 211 inhibits protein kinase A in Schwann cells to modulate neuregulin 1 type III-driven myelination [PDF]
et al.,, Mogha, Amit, Monk, Kelly
core +1 more source
Atypical manifestation of late onset limb girdle muscular dystrophy presenting with recurrent falling and shoulder dysfunction: a case report [PDF]
core +1 more source
JADID NAMOYONDALARI MEROSINING BUGUNGI KUNDAGI AHAMIYATI
In this article, an opinion is expressed about the scientific heritage of Jadids, which came to the field of history as an educational, socio-political movement at the end of the XIX th century and the beginning of the XX th century. It is noted that the scientific and educational heritage of the ancients is similar to the educational policy ...
openaire +1 more source
Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families. [PDF]
Safwat S +5 more
europepmc +1 more source
Abduqodir Shakuriy pedagogik merosining bugungi ahamiyati
Ushbu maqolada jadidchilik harakatining faol namoyandalaridan biri Abduqodir Shakuriyning ma’rifatparvarlik qarashlari keng qamrovda tahlil qilinadi. Tadqiqotda Shakuriyning ta’limni isloh qilish, yangi usul maktablarini joriy etish, milliy o‘zlikni anglashni kuchaytirish, yosh avlodni axloqiy komillik ruhida tarbiyalash hamda jamiyatni ma’rifat ...
Begoyim Umidbek-qizi Toshmuhammadova +1 more
openaire +1 more source
Prevalence of human T-cell leukemia virus type 1 associated inflammatory myopathies (HAIM) in Salvador, Brazil. [PDF]
Viriato ARF +7 more
europepmc +1 more source
Editorial: Rare diseases research and diagnosis in low- and middle-income countries. [PDF]
Gonzaga-Jauregui C +2 more
europepmc +1 more source

