Results 101 to 110 of about 2,066 (126)

Stem cell-based approach to identify regulatory TFs during mammalian cell differentiation. [PDF]

Stem Cell Reports
Pei Y, Li S, Garipler G, Kamimoto K, Mazzoni EO.   +4 more
europepmc   +1 more source

Distinct Antibody Fc-profiles in Lymph During Homeostasis and Chronic HIV Infection. [PDF]

Pathog Immun
McNamara RP, Butler AL, Dolatshahi S, Taylor S, Dori Y, Frank I, Itkin MG, Betts MR, Alter G.   +8 more
europepmc   +1 more source

A novel <i>ZNF699</i> mutation in a patient with DEGCAGS syndrome and severe B cell depletion. [PDF]

J Hum Immun
Giardino G, Romano R, Squeo GM, Toriello E, De Rosa A, Ammendola A, Gemma G, Rzasa J, Kerkhof J, di Venere E, Cantelli M, Cirillo E, Nigro V, Sadikovic B, Pignata C, Merla G.   +15 more
europepmc   +1 more source

Functional antibody signatures following therapeutic immunization in Simian and Human immunodeficiency virus infection. [PDF]

NPJ Vaccines
Ilan S, Bartsch Y, Jung W, Kliuchnikov E, Roy V, Bonifer R, Walker-Sperling VEK, Borducchi EN, Nkolola JP, Lauffenburger DA, Stieh DJ, Barouch DH, Julg B.   +12 more
europepmc   +1 more source

CRISPRi-based screen of autism spectrum disorder risk genes in microglia uncovers roles of ADNP in microglia endocytosis and synaptic pruning. [PDF]

Mol Psychiatry
Teter OM, McQuade A, Hagan V, Liang W, Dräger NM, Sattler SM, Holmes BB, Castillo VC, Papakis V, Leng K, Boggess S, Nowakowski TJ, Wells J, Kampmann M.   +13 more
europepmc   +1 more source

Transcriptomic Analysis Uncovers an Unfolded Protein Response in ADNP Syndrome. [PDF]

Mol Cell Biol
Bieluszewska A, Wulfridge P, Fang KC, Hong Y, Sawada T, Erwin J, Song H, Ming GL, Sarma K.   +8 more
europepmc   +1 more source

Genetic architecture of patients with autism spectrum disorder - data analysis based on the literature review. [PDF]

BMC Med Genomics
Ręka G, Wojciechowska K, Lejman M.
europepmc   +1 more source

Remodeling Activity of ChAHP Restricts Transcription Factor Access to Chromatin

Ahel J, Mohn F, Schwaiger M, Kaaij L, Steiner J, Moreno EPF, Hess D, Bühler M.   +7 more
europepmc   +1 more source

Ultrarare Variants in DNA Damage Repair and Mitochondrial Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome and Acute Behavioral Regression in Neurodevelopmental Disorders.

Dev Neurosci
Vettiatil D, Soorajkumar A, Dubin RA, Pedrosa EM, Schornagel A, Lambert JS, Costa IP, McDonald J, Swagemakers SMA, van der Spek PJ, Frankovich J, Cunningham JL, Lachman HM.   +12 more
europepmc   +1 more source