Results 161 to 170 of about 36,508 (354)

Prenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia

Prenatal Diagnosis, EarlyView.
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear, Billie Lianoglou, Ugur Hodoglugil, W. Patrick Devine, Ashutosh Lal, Juan Gonzalez, Teresa N. Sparks   +6 more
wiley   +1 more source

METAMORPHOSIS OF HUMAN AMNION CELLS INDUCED BY PREPARATIONS OF INTERFERON

, 1961
Ion Gresser
openalex   +1 more source

Hemophilia A: An Ideal Disease for Prenatal Therapy

Prenatal Diagnosis, EarlyView.
ABSTRACT Hemophilia A (HA) is the most common inherited coagulation defect. Current state‐of‐the‐art treatment consists of frequent administration of prophylactic infusions of coagulation factor VIII (FVIII) protein or bispecific antibodies that replace the cofactor function of FVIIIa to maintain hemostasis. However, these treatments are far from ideal,
Christopher D. Porada, Anthony Atala, Graça Almeida‐Porada   +2 more
wiley   +1 more source

Cell Type-Specific Regulation of Fetal Fibronectin Expression in Amnion: Conservation of Glucocorticoid Responsiveness in Human and Nonhuman Primates1 [PDF]

, 2000
Yuehong Ma, Charles J. Lockwood, Ari L. Bunim, Dino A. Giussani, Peter W. Nathanielsz, Seth Guller   +5 more
openalex   +1 more source

A Prospective Evaluation of the Diagnostic Utility for Low‐Coverage Genome Sequencing in Prenatal Samples: A Comparison With Chromosomal Microarray Analysis

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective The present study aimed to evaluate the efficacy of LC‐GS in detecting clinically relevant chromosomal abnormalities in comparison with conventional CMA within a prenatal context. Methods We conducted a prospective study involving 200 amniotic fluid samples.
Yan Yin, Yuxia He, Chun Chen, Yanyan He, Jin Wang, Shengfang Qin, Hongna Wang, Kun Ma, Dahui Hu, Rui Xiao, Gang Wang, Xueyan Wang   +11 more
wiley   +1 more source

Observations on the Fine Structure and Replication of Varicella Virus in Cultivated Human Amnion Cells

, 1968
B. G. Achong, E.V. Meurisse
openalex   +1 more source

Benefits of maternal corticosteroid therapy in infants weighing ≤1000 grams at birth after preterm rupture of the amnion [PDF]

, 2000
Jeffrey M. Perlman
openalex   +1 more source

Global Delivery of Foetal Sequencing: Do We Need Some Standardisation?

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective The development of sequencing technologies has resulted in rapid expansion in the testing available for foetuses with structural anomalies to diagnose monogenic disorders. To understand the variability in how foetal sequencing services are delivered, we developed a survey that focussed on the scope of testing, any parallel testing ...
Natalie J. Chandler, Zandra C. Deans
wiley   +1 more source

Morphological Changes And Resistance To Vaccinia Virus Induced In Human Amnion Cells By Yeast Extract

, 1971
Atonu Chakrabortty, T. S. L. Beswick
openalex   +1 more source

Enhanced dehydroepiandrosterone synthesis by amnion compared to chorion: A comparative study using the reverse-isotope dilution technique [PDF]

, 2001
A. Loganath, K. L. Peh, Y. C. Wong, S. C. Ng   +3 more
openalex   +1 more source