521-11-9

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Genetic linkage analysis in recombinant inbred mice of P40, a putative clone for the high-affinity laminin receptor.

P J Douville et al.

Mammalian genome : official journal of the International Mammalian Genome Society, 3(8), 438-446 (1992-01-01)

Recombinant inbred (RI) mice were used to genetically map sequences of a 43-kDa protein, P40, that was originally identified as a high-affinity laminin receptor. More recent data have implicated this protein in development of the retina (Rabacchi et al. Development

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.

Hannu Laaksovirta et al.

The Lancet. Neurology, 9(10), 978-985 (2010-08-31)

The genetic cause of amyotrophic lateral sclerosis (ALS) is not well understood. Finland is a well suited location for a genome-wide association study of ALS because the incidence of the disease is one of the highest in the world, and

Treatment reduction for children and young adults with low-risk acute lymphoblastic leukaemia defined by minimal residual disease (UKALL 2003): a randomised controlled trial.

Ajay Vora et al.

The Lancet. Oncology, 14(3), 199-209 (2013-02-12)

Minimal residual disease (MRD) is the most sensitive and specific predictor of relapse risk in children with acute lymphoblastic leukaemia (ALL) during remission. We assessed whether treatment intensity could be adjusted for children and young adults according to MRD risk

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