Results 281 to 290 of about 122,453 (313)

Mutational profiles of spontaneous and radiation-related mammary carcinomas in a rat model of Brca1 haploinsufficiency. [PDF]

Sci Rep
Nakamura Y, Daino K, Ishikawa A, Kakinuma S, Nishimura-Yano Y, Nagata K, Takabatake M, Nishimura M, Mashimo T, Inoue K, Imaoka T.   +10 more
europepmc   +1 more source

Heimler Syndrome Caused by Novel <i>PEX6</i> Variants: Clinical and Genetic Characterization in a Saudi Cohort. [PDF]

Genes (Basel)
AlMoallem B.
europepmc   +1 more source

A Partial <i>UMOD</i> Deletion Results in Altered Uromodulin Synthesis and Autosomal-Dominant Tubulointerstitial Kidney Disease-Uromodulin. [PDF]

Kidney Med
Fagnoul S, Ghisdal L, Marangoni M, Detry C, Dacremont-Rodriguez P, Bisteau X, Imbault V, Catalano C, Smits G, Le Moine A, Migeotte I.   +10 more
europepmc   +1 more source

A Scoping Review on Genetic Mutations and Single-Nucleotide Polymorphisms Associated with Pectus Excavatum. [PDF]

J Multidiscip Healthc
Barman S, Momin L, Islam R, Shing MS, Ranjan R, Waterhouse B, Dunning J.   +6 more
europepmc   +1 more source

Comprehensive assessment of the genomic stability of human induced pluripotent stem cells for clinical applications. [PDF]

Stem Cell Res Ther
Zhang K, Na T, Jia C, Yuan X, Guo M, Yang X, Li M, Jia W, Bai Z, Lu J, Liu Z, Meng S.   +11 more
europepmc   +1 more source