Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Expanding the genetic and phenotypic spectrum of the subcortical maternal complex genes in recurrent preimplantation embryonic arrest.

Clinical genetics - 1 Feb 2021

Zheng Wei, Hu Huiling, Dai Jing, Zhang Shuoping, Gu Yifan, Dai Can, Guo Jing, Xu Xinxin, Li Yuan, Zhang Shunji, Hu Liang, Gong Fei, Lu Guangxiu, Lin Ge

Abstract excerpt

The subcortical maternal complex (SCMC) is an oocyte-to-embryo-specific maternal functional module. Some variants of SCMC genes that contribute to preimplantation embryonic arrest have been identified. However, more novel variants should be identified to broaden the genetic and phenotypic spectrum of SCMC genes and establish their roles in embryonic development. We identified 13 novel variants in the SCMC genes,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abortion, Spontaneous
Share to Apoptosis Regulatory Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Autoantigens

Share to Blastocyst

Share to Co-Repressor Proteins

Share to Infertility, Female

Share to Multiprotein Complexes

Share to Time-Lapse Imaging

Source

Identifiers

PMID: 33020905
DOI: 10.1111/cge.13858

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Expanding the genetic and phenotypic spectrum of the subcortical maternal complex genes in recurrent preimplantation embryonic arrest.PMID 33020905Read ↗

Mutations in OOEP and NLRP5 identified in infertile patients with early embryonic arrest.Semantic proximity Read ↗

Identification of Novel SCMC Gene Variants Associated With Early Embryonic Arrest.Semantic proximity Read ↗

Variants in NLRP2 and ZFP36L2, non-core components of the human subcortical maternal complex, cause female infertility with embryonic development arrestSemantic proximity Read ↗

Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.Semantic proximity Read ↗

NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest.Semantic proximity Read ↗

Identification of a human subcortical maternal complexSemantic proximity Read ↗

Two Novel Protein-Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal Complex.Semantic proximity Read ↗

Subcortical Maternal Complex in Female Infertility: A Transition from Animal Models to Human Studies.Semantic proximity Read ↗

Novel Homozygous PADI6 Variants in Infertile Females with Early Embryonic ArrestSemantic proximity Read ↗

Genetic factors as potential molecular markers of human oocyte and embryo quality.Semantic proximity Read ↗

Novel variants in PADI6 genes cause female infertility due to early embryo arrest.Semantic proximity Read ↗

NLRPs, the subcortical maternal complex and genomic imprinting.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.