Results 161 to 170 of about 4,156 (218)

OCRL1 Deficiency Affects the Intracellular Traffic of ApoER2 and Impairs Reelin-Induced Responses. [PDF]

Biomolecules
Fuentealba LM, Pizarro H, Marzolo MP.
europepmc   +1 more source

Genetic analysis and clinical characteristics of sporadic and familial congenital cataracts in southern Chinese families. [PDF]

Front Genet
Huang T, Sun HS, Liu YN, Xie QL, Liu Y, Miao XC, Wu W, Li J.   +7 more
europepmc   +1 more source

Manifestations tangentielles de la néotectonique quaternaire dans la région de Mateur-Tebourba (zone des diapirs), Tunisie septentrionale [PDF]

, 1983
Fournet, André
core  

The European Investment Bank in 1987 [PDF]

, 1988

core  

Identifying preeclampsia-associated key module and hub genes via weighted gene co-expression network analysis. [PDF]

Sci Rep
Li J, Jiang L, Kai H, Zhou Y, Cao J, Tang W.   +5 more
europepmc   +1 more source

Updated Gene Therapy for Renal Inborn Errors of Metabolism. [PDF]

Genes (Basel)
Hergenrother S, Husein M, Thompson C, Kalina E, Raina R.   +4 more
europepmc   +1 more source

Genetic aetiology of global developmental delay and intellectual disability in Africa: a scoping review. [PDF]

Front Genet
Dukuze N, Hitayezu J, Uyisenga JP, Hakizimana O, Bours V, Uwineza A, Alagbonsi AI.   +6 more
europepmc   +1 more source

Structural basis for binding of RILPL1 to TMEM55B reveals a lysosomal platform for adaptor assembly through a conserved TBM motif

Waschbüsch D, Pal P, Nirujogi RS, Cavin M, Singh J, Alessi DR, Khan AR.   +6 more
europepmc   +1 more source

Current insights into renal ciliopathies: what can genetics teach us? [PDF]

core   +1 more source

Lowe Syndrome and Me: a co-creation video series connecting patients, caregivers, and researchers. [PDF]

Front Cell Dev Biol
Haugen T, Gallop JL, Doerflinger H.
europepmc   +1 more source