Cargando…

First report of inherited protein S deficiency caused by paternal PROS1 mosaicism

Detalles Bibliográficos
Autores principales:	Nagaya, Satomi, Maruyama, Keiko, Watanabe, Atsushi, Meguro-Horike, Makiko, Imai, Yuta, Hiroshima, Yuki, Horike, Shin-Ichi, Kokame, Koichi, Morishita, Eriko
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Fondazione Ferrata Storti 2021
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719071/ https://www.ncbi.nlm.nih.gov/pubmed/34647440 http://dx.doi.org/10.3324/haematol.2021.278527

Ejemplares similares

Topical estrogen application promotes cutaneous wound healing in db/db female mice with type 2 diabetes
por: Mukai, Kanae, et al.
Publicado: (2022)

Bromodomain protein BRD4 inhibitor JQ1 regulates potential prognostic molecules in advanced renal cell carcinoma
por: Sakaguchi, Takashi, et al.
Publicado: (2018)

MUSASHI‐2 confers resistance to third‐generation EGFR‐tyrosine kinase inhibitor osimertinib in lung adenocarcinoma
por: Yiming, Reheman, et al.
Publicado: (2021)

Epigenetic Regulation of Aldosterone Synthase Gene by Sodium and Angiotensin II
por: Takeda, Yoshimichi, et al.
Publicado: (2018)

ELISA-Based Detection System for Protein S K196E Mutation, a Genetic Risk Factor for Venous Thromboembolism
por: Maruyama, Keiko, et al.
Publicado: (2015)

Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism
por: Tung, Joanna Yuet-ling, et al.
Publicado: (2020)

UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons
por: Lopez, S. Jesse, et al.
Publicado: (2017)

Aging-associated impairment in metabolic compensation by subcutaneous adipose tissue promotes diet-induced fatty liver disease in mice
por: Taketani, Hiroyoshi, et al.
Publicado: (2019)

Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis Deformation
por: Guo, Long, et al.
Publicado: (2016)

Potential therapeutic target secretogranin II might cooperate with hypoxia‐inducible factor 1α in sunitinib‐resistant renal cell carcinoma
por: Fukumoto, Wataru, et al.
Publicado: (2023)

A maternal high-fat diet induces fetal origins of NASH-HCC in mice
por: Takiyama, Takao, et al.
Publicado: (2022)

Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments
por: Maruyama, Keiko, et al.
Publicado: (2020)

Cancer stem-like properties and gefitinib resistance are dependent on purine synthetic metabolism mediated by the mitochondrial enzyme MTHFD2
por: Nishimura, Tatsunori, et al.
Publicado: (2018)

Cannabis and Paternal Epigenetic Inheritance
por: Mazzeo, Filomena, et al.
Publicado: (2023)

Targeting cis-regulatory elements of FOXO family is a novel therapeutic strategy for induction of leukemia cell differentiation
por: Kurayoshi, Kenta, et al.
Publicado: (2023)

Alpha‐HIT assay: A new assay for heparin‐induced thrombocytopenia antibody detection using FcγRIIa‐coated beads and Alpha technology
por: Maruyama, Keiko, et al.
Publicado: (2022)

A Case of Treatment With Dabigatran for Cerebral Venous Thrombosis Caused by Hereditary Protein C Deficiency
por: Fukushima, Taiki, et al.
Publicado: (2021)

Protein C Gene Mutation in an Older Adult Patient with Clostridium perfringens Septicemia-Related Visceral Vein Thrombosis
por: Kanosue, Kiyoko, et al.
Publicado: (2021)

An uncommon inheritance pattern in Niemann-Pick disease type C: identification of probable paternal germline mosaicism in a Mexican family
por: Cervera-Gaviria, Marivi, et al.
Publicado: (2016)

Baf53a is involved in survival of mouse ES cells, which can be compensated by Baf53b
por: Zhu, Bo, et al.
Publicado: (2017)

Proton-conductive coordination polymer glass for solid-state anhydrous proton batteries
por: Ma, Nattapol, et al.
Publicado: (2021)

Active K‐RAS induces the coherent rotation of epithelial cells: A model for collective cell invasion in vitro
por: Hirata, Eishu, et al.
Publicado: (2018)

Protein S K196E mutation reduces its cofactor activity for APC but not for TFPI
por: Maruyama, Keiko, et al.
Publicado: (2018)

Occasional paternal inheritance of the germline-restricted chromosome in songbirds
por: Pei, Yifan, et al.
Publicado: (2022)

DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex
por: Miyano, Masaru, et al.
Publicado: (2008)

Paternal inheritance of growth in fish pursuing alternative reproductive tactics
por: Wirtz-Ocaňa, Sabine, et al.
Publicado: (2013)

Consequences of paternally inherited effects on the genetic evaluation of maternal effects
por: Varona, Luis, et al.
Publicado: (2015)

Paternal chronic colitis causes epigenetic inheritance of susceptibility to colitis
por: Tschurtschenthaler, Markus, et al.
Publicado: (2016)

Inheritance of paternal DNA damage by histone-mediated repair restriction
por: Wang, Siyao, et al.
Publicado: (2022)

Paternal Low-Level Mosaicism-Caused SATB2-Associated Syndrome
por: Qian, Yeqing, et al.
Publicado: (2019)

Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism
por: Chandran, Suresh, et al.
Publicado: (2013)

Diet and Transgenerational Epigenetic Inheritance of Breast Cancer: The Role of the Paternal Germline
por: da Cruz, Raquel Santana, et al.
Publicado: (2020)

Paternal leakage of mitochondrial DNA and maternal inheritance of heteroplasmy in Drosophila hybrids
por: Polovina, Eirini-Slavka, et al.
Publicado: (2020)

Paternal Inheritance of Bisphenol A Cardiotoxic Effects: The Implications of Sperm Epigenome
por: Lombó, Marta, et al.
Publicado: (2021)

A systematic scientometric review of paternal inheritance of acquired metabolic traits
por: Crisóstomo, Luís, et al.
Publicado: (2023)

Effect on Plasma Protein S Activity in Patients Receiving the Factor Xa Inhibitors
por: Terakami, Takako, et al.
Publicado: (2022)

Inheritance of Pigeonpea Sterility Mosaic Disease Resistance in Pigeonpea
por: Daspute, Abhijit, et al.
Publicado: (2014)

Identification of paternal germline mosaicism by MicroSeq and targeted next‐generation sequencing
por: Dai, Congling, et al.
Publicado: (2020)

Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation
por: Tüngler, Victoria, et al.
Publicado: (2019)

MED13L-related intellectual disability due to paternal germinal mosaicism
por: Bessenyei, Beáta, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_j71oi938tat1m25k43goq170rl