The impact of Lama2-deficiency on cell cycle regulation and survival
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.
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Characterizing the impact of LAMA2-deficiency in cancer cell lines
Tese de mestrado, Biologia Evolutiva e Desenvolvimento, 2023, Universidade de Lisboa, Faculdade de ...
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Clinical and functional outcome measures in LAMA2-related muscular dystrophy and SELENON-related myopathy; a 1.5-year natural history study. [PDF]
de Laat ECM +5 more
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Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron disease. [PDF]
Lok HC +20 more
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Low LAMA2 expression may affect drug resistance and prognosis in ovarian cancer via positive LGR5 coexpression. [PDF]
Du Z +7 more
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Glomerular basement membrane structural integrity dictates trans-tissue deposition of laminin in the kidney. [PDF]
Omachi K +7 more
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Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep. [PDF]
Zhang L +8 more
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Integrated Approach to Diagnosing Limb-Girdle Muscular Dystrophies in Resource-Limited Settings. [PDF]
Yousaf H +23 more
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Alternative Splicing Dynamics Associated with Nutritional Transition and Starvation-Induced PNR in <i>Leiocassis longirostris</i> Larvae. [PDF]
Guan S, Si X, Tang Y, Li Q, Zhou C.
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Natural history of LAMA2 related dystrophies
Clara Gontijo Camelo +7 more
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