Results 171 to 180 of about 578,006 (359)
Maternal Cigarette Smoke Exposure Exaggerates the Behavioral Defects and Neuronal Loss Caused by Hypoxic-Ischemic Brain Injury in Female Offspring [PDF]
Taida Huang +13 more
openalex +1 more source
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen +5 more
wiley +1 more source
What can challenging reproductive contexts tell us about the rat's maternal behavior? [PDF]
Agrati D, Uriarte N.
europepmc +1 more source
Maternal Programming of Reproductive Function and Behavior in the Female Rat [PDF]
Nicole M. Cameron
openalex +1 more source
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle +10 more
wiley +1 more source
Maternal Behavior in Beef Cattle: The Physiology, Assessment and Future Directions-A Review. [PDF]
Nevard RP +4 more
europepmc +1 more source
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide +10 more
wiley +1 more source
Abnormal maternal behavior in mice lacking phospholipase Cβ1. [PDF]
Kim HJ, Jang J, Koh HY.
europepmc +1 more source
ABSTRACT Autosomal recessive loss‐of‐function variants in PPP1R13L cause an ultra‐rare cardiocutaneous syndrome characterized by rapidly progressive arrhythmogenic cardiomyopathy (ACM). PPP1R13L encodes iASPP, which has two potentially overlapping mechanisms driving ACM as both a regulator of NFκB‐mediated inflammation and a binding partner within the ...
Aaron Renberg +9 more
wiley +1 more source
Differential associations of maternal behavior to preschool boys' and girls' executive function. [PDF]
Vrantsidis DM +3 more
europepmc +1 more source

