Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lokesh Pimpale"'
Autor:
Kriti Chaplot, Lokesh Pimpale, Balaji Ramalingam, Senthilkumar Deivasigamani, Siddhesh S. Kamat, Girish S. Ratnaparkhi
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 2 (2019)
Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to
Externí odkaz:
https://doaj.org/article/3dd5f25ebd454506bed46a64f75f78b8
Autor:
Clara Schmidt, Alison Deyett, Tobias Ilmer, Aranxa Torres Caballero, Simon Haendeler, Lokesh Pimpale, Michael A. Netzer, Lavinia Ceci Ginistrelli, Martina Cirigliano, Estela Juncosa Mancheno, Daniel Reumann, Katherina Tavernini, Steffen Hering, Pablo Hofbauer, Sasha Mendjan
Publikováno v:
SSRN Electronic Journal.
The number one cause of human fetal death are defects in heart development. Because the human embryonic heart is inaccessible, and the impacts of mutations, drugs, and environmental factors on the specialized functions of different heart compartments
Autor:
Lokesh Pimpale, Balaji Ramalingam, Siddhesh S. Kamat, Girish S. Ratnaparkhi, Senthilkumar Deivasigamani, Kriti Chaplot
Publikováno v:
Disease Models & Mechanisms.
Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to
Autor:
Kriti, Chaplot, Lokesh, Pimpale, Balaji, Ramalingam, Senthilkumar, Deivasigamani, Siddhesh S, Kamat, Girish S, Ratnaparkhi
Publikováno v:
Disease Models & Mechanisms
Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to