Results 91 to 100 of about 3,944 (168)

The impact of Lama2-deficiency on cell cycle regulation and survival

open access: yes, 2022
A distrofia muscular congénita deficiente na cadeia α2 da laminina (LAMA2-CMD) é causada por mutações recessivas no gene LAMA2. Esta doença neuromuscular é diagnosticada à nascença ou nos primeiros meses de vida e é caracterizada por hipotonia e fraqueza muscular grave.
openaire   +1 more source

Characterizing the impact of LAMA2-deficiency in cancer cell lines

open access: yes, 2023
Tese de mestrado, Biologia Evolutiva e Desenvolvimento, 2023, Universidade de Lisboa, Faculdade de ...
openaire   +1 more source

Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron disease. [PDF]

open access: yesHum Mol Genet
Lok HC   +20 more
europepmc   +1 more source

Glomerular basement membrane structural integrity dictates trans-tissue deposition of laminin in the kidney. [PDF]

open access: yesCell Rep
Omachi K   +7 more
europepmc   +1 more source

Integrated Approach to Diagnosing Limb-Girdle Muscular Dystrophies in Resource-Limited Settings. [PDF]

open access: yesHum Mutat
Yousaf H   +23 more
europepmc   +1 more source

Natural history of LAMA2 related dystrophies

open access: yesArquivos de Neuro-Psiquiatria
Clara Gontijo Camelo   +7 more
openaire   +1 more source

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