Results 151 to 160 of about 4,772 (187)

Genetic polymorphisms of <i>LMX1B</i> and <i>MLXIP</i> are associated with hip osteoarthritis in the Chinese population. [PDF]

Biomark Med
Chen C, Kong D, Wang P, Li M, Gui R.
europepmc   +1 more source

Hormone-switching islet cells: parallels to transmitter-switching neurons. [PDF]

Front Cell Dev Biol
Dor Y, Spitzer NC.
europepmc   +1 more source

Comparative Multi-Omics Analysis of the Iridocorneal Angle Identifies an Immune-Fibrotic Profile in the DBA/2J Glaucoma Mouse Model. [PDF]

Mol Cell Proteomics
Shim MS, Grimsrud A, Desikan V, Sung MS, Liton PB.   +4 more
europepmc   +1 more source

Integrative multi-omics analysis deciphers the regulatory mechanisms of egg weight traits in chickens. [PDF]

Poult Sci
Ding J, Liu X, Nawaz AH, Leng D, Li N, Ge D, Li D, Feng C.   +7 more
europepmc   +1 more source

Deciphering the shared genetic structure between hip osteoarthritis and femoral neck bone mineral density. [PDF]

Front Genet
Zhou J, Na J, Jiang Z, Dou X, Wang S, Li H, Kang J.   +6 more
europepmc   +1 more source

Neph1 is required for neurite branching and is negatively regulated by the PRRXL1 homeodomain factor in the developing spinal cord dorsal horn. [PDF]

Neural Dev
Baltar J, Miranda RM, Cabral M, Rebelo S, Grahammer F, Huber TB, Reguenga C, Monteiro FA.   +7 more
europepmc   +1 more source

Gene expression profile in colon cancer therapeutic resistance and its relationship with the tumor microenvironment. [PDF]

Front Bioinform
Doria PG, Rocha GV, Bertoni VD, Dos Santos RSB, Araújo-Pereira M, Gurgel C.   +5 more
europepmc   +1 more source

Evidence for therapeutic use of cannabidiol for nail-patella syndrome-induced pain in a real-world pilot study. [PDF]

Sci Rep
Lebret T, Hatton S, Callebert J, Cormier-Daire V, Greco C.   +4 more
europepmc   +1 more source

Case report: A novel R246L mutation in the LMX1B homeodomain causes isolated nephropathy in a large Chinese family. [PDF]

Medicine (Baltimore)
Li X, Fan J, Fu R, Peng M, He J, Chen Q, Wang S, Chen C.   +7 more
europepmc   +1 more source

Whole-Exome Sequencing for Molecular Diagnosis of Paediatric Nephrotic Syndrome in Africa: A Call for Implementation. [PDF]

Genes (Basel)
Gcobo T, Katsukunya JN, Lamola L, Awany D, Ndadza A, Dandara C, Mnika K.   +6 more
europepmc   +1 more source