Results 101 to 110 of about 78,165 (161)

Genetic Analysis of Pitt-Hopkins Syndrome Caused by a Novel Splicing Variant (c.1146+3A>T) in the TCF4 Gene. [PDF]

Mol Genet Genomic Med
Shen W, Zhang Y, Wu J, Zhao J, Lv Y, Tang X.   +5 more
europepmc   +1 more source

Intra-amniotic transplantation of APOM-modified BMSCs facilitates neural repair in spina bifida by improving vascular endothelial integrity. [PDF]

Cell Commun Signal
Liu Y, Zhao Z, Chen L, Wei X, Ding D, Cao S, Gu H, Liu D, Chen L, Jia S, Luo W, Cai Z, Wu Q, Huang T, Huang W, He Y, Xue J, Yuan Z, Ma W.   +18 more
europepmc   +1 more source

Derivation and Pluripotency Validation of Six iPSC Lines From Amniotic Fluid Carrying Intermediate α-Thalassemia Genotypes (--^3.7/α^SEA and --^4.2/α^SEA). [PDF]

Stem Cells Int
Chen Q, Jiang X, Xue X, Zhou Y, Huang Y, Sun F, Ma Y.   +6 more
europepmc   +1 more source

Body stalk anomalies and their relationship to amniotic band disruption complex in six cats. [PDF]

J Feline Med Surg
Martín-Alguacil N, Cozar JM, Avedillo L.   +2 more
europepmc   +1 more source

RAGE phosphorylation by CK2 in human epithelial cell model: Modulation of connexin 43 expression. [PDF]

iScience
Coste K, Hesse AM, Marceau G, Filhol O, Cochet C, Freton C, Blanchon L, Sapin V, Belville C.   +8 more
europepmc   +1 more source

Pseudoamniotic Band Sequence Risk Factors following Fetoscopic Laser for Twin-Twin Transfusion Syndrome.

Fetal Diagn Ther
Lemoine FV, Backley S, Vilchez-Lagos G, Espinoza J, Hernandez-Andrade E, Johnson A, Papanna R, Bergh E.   +7 more
europepmc   +1 more source

Evaluation and management of DMD gene copy number variations detected by prenatal SNP-array testing. [PDF]

BMC Med Genomics
Hu J, Pang J, Hu R, Zhou L, Yu W, Xi H, Luo Y, Yang S, Tang W, Hu A, Chen J, Peng Y.   +11 more
europepmc   +1 more source

Exploring Upper Limb Malformation Associated With Cornelia De Lange Syndrome: A Clinical Case Report. [PDF]

Case Rep Obstet Gynecol
Kurniawan AP, Abdurrazak G, Muthalib AA, Hasani RDK.   +3 more
europepmc   +1 more source

11β-HSD2 buffers fetal glucocorticoid exposure inducing <i>Per1</i> expression under maternal stress. [PDF]

PNAS Nexus
Yabumoto K, Umemura Y, Watanabe H, Endo Y, Koike N, Kakibuchi A, Sugimoto A, Mori T, Kondoh G, Yagita K.   +9 more
europepmc   +1 more source

Using SNP microarray to distinguish mosaicism from chimerism in a phenotypically normal male newborn with prenatal 46,XX/46,XY karyotype. [PDF]

Mol Cytogenet
Chen JC, Su PH, Jong YJ, Huang PC, Cheng SY, Lin YH.   +5 more
europepmc   +1 more source