Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

about

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

Item

http://www.wikidata.org/entity/Q52310129

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

@en

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

@nl

type

Item

label

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

@en

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

@nl

prefLabel

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

@en

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.

@nl

P1476

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles

@en

P2093

Ao Asangla

http://www.w3.org/2001/XMLSchema#string

Bo Huang

http://www.w3.org/2001/XMLSchema#string

HanJin Yang

http://www.w3.org/2001/XMLSchema#string

JianHua Qian

http://www.w3.org/2001/XMLSchema#string

Maryam Rezaei

http://www.w3.org/2001/XMLSchema#string

Ngoc Minh Phuong Nguyen

http://www.w3.org/2001/XMLSchema#string

Qi Cheng

http://www.w3.org/2001/XMLSchema#string

XiaoFei Zhang

http://www.w3.org/2001/XMLSchema#string

YongLing Tao

http://www.w3.org/2001/XMLSchema#string

P2860

A subcortical maternal complex essential for preimplantation mouse embryogenesis

Role for PADI6 and the cytoplasmic lattices in ribosomal storage in oocytes and translational control in the early mouse embryo

Peptidylarginine deiminase (PAD) 6 is essential for oocyte cytoskeletal sheet formation and female fertility

Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest

TLE6 mutation causes the earliest known human embryonic lethality.

Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutations.

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

STR DNA genotyping of hydatidiform moles in South China.

Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.

Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.

P2888

s41431-018-0141-3

P304

1007-1013

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/S41431-018-0141-3

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Jacek Majewski

Rima Slim

P577

2018-04-25T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29693651

http://www.w3.org/2001/XMLSchema#string

P921

miscarriage

P932

6018785

http://www.w3.org/2001/XMLSchema#string