Results 181 to 190 of about 37,180 (356)

Cardiovascular defects associated with abnormalities in midline development in the Loop-tail mouse mutant [PDF]

, 2001
Anderson, RH, Conway, SJ, Copp, AJ, Gerrelli, D, Greene, NDE, Henderson, DJ, Murdoch, JN   +6 more
core   +1 more source

Evaluation of Keratinized Tissue Augmentation Using Amnion/Chorion Allograft vs. Autogenous Connective Tissue in Implant Therapy: A Retrospective Study [PDF]

Nicola De Angelis, Paolo Pesce, Zethy Hanum Mohamed Kassim, Catherine Yumang, Domenico Baldi, María Menini   +5 more
openalex   +1 more source

Diagnostic Value of Exome Sequencing in Isolated Polyhydramnios

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield of exome sequencing (ES) in isolated polyhydramnios. Methods This retrospective study included 40 cases of isolated polyhydramnios. All patients underwent screening for gestational diabetes mellitus (GDM) and chromosomal microarray analysis (CMA).
Vered Offen Glassner, Adi Botvinik, Adi Mory, Adi Reches, Karina Krajden Haratz, Britannia Morgan Fleming, Hagit Baris Feldman, Lena Sagi‐Dain, Mordechai Shohat, Rayna Joy Goldstein, Yuval Yaron, Michal Levy   +11 more
wiley   +1 more source

TFAP2A+ Embryonic Progenitor Cells Undergo Fate Diversification to Give Rise to Human Amnion, Germline, and Mesoderm

Auriana Arabpour, Jonathan DiRusso, Qiuya Wu, Mark Larsen, Young Sun Hwang, Elsie Jacobson, Thi Xuan Ai Pham, Nicole Agranonik, Megan Sparrow, Vernon Monteiro, Zhuan Bian, Nicolás Peláez-Restrepo, A Marin, Vincent Pasque, Kathrin Plath, Amander T. Clark   +15 more
openalex   +1 more source

Comparison of reactive oxygen species metabolisms in human amnion mesenchymal stem and MG-63 cells

, 2021
Sergejs Zavadskis
openalex   +1 more source

Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal Cases

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Spinal dysraphism (SD) results from incomplete neural tube closure and encompasses a heterogeneous group of congenital anomalies with genetic and environmental etiologies. Although genetic contributions are recognized, causative variants remain insufficiently defined, and the clinical implications of extended genetic testing on ...
I. Bedei, A. Feresin, R. Zemet, D. Berner, D. Polidori, K. Fröbius, A. Skakkebæk, R. Axt‐Fliedner, M. Shoukier, C. Keil   +9 more
wiley   +1 more source

Biomaterials for fetal membrane repair in preterm premature rupture of membranes: advances in tissue engineering strategies. [PDF]

J Biol Eng
Fan L, Liu Z, Li X, Ji Y, Li H.
europepmc   +1 more source

Oxidative stress-induced TGF-beta/TAB1-mediated p38MAPK activation in human amnion epithelial cells† [PDF]

, 2018
Lauren Richardson, Christopher Luke Dixon, Leopoldo Aguilera-Aguirre, Ramkumar Menon   +3 more
openalex   +1 more source

Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective We aimed to characterize the fetal features across gestation and describe genotype‐phenotype correlations for pregnancies with fetal RASopathies that were more severely affected as they presented with at least one abnormal fluid collection.
Natalie B. Gulrajani, John Boscardin, Billie R. Lianoglou, Katie Tick, Carmen M. A. Santoli, Kristen A. Miller, Angie C. Jelin, Lorraine Dugoff, Rose Giardine, Cori Feist, Rachel Pilliod, Stephanie Dukhovny, Kelly Gilmore, Neeta L. Vora, Aisling Murphy, Peter N. Robinson, Mary E. Norton, Teresa N. Sparks   +17 more
wiley   +1 more source

Osteomyelitis as a Rare Complication in an 8-Year-Old Boy With Beta Thalassemia: A Case Report. [PDF]

Clin Case Rep
Soleja FK, Mujtaba A, Imran A, Mirza MO, Anan M.   +4 more
europepmc   +1 more source