Copertina

Identification of two novel c.11_15dup; c.17G>A variations in the ABO*B.01 allele giving rise to a weak B phenotype

Fuente: Wiley Open Access

Salvato in:

Dettagli Bibliografici
Autori principali:	Hongbo Liu, Hongmei Liu, Rong Gui, Rong Huang, Xing Chen, Xiaohui Dai, Shiqiao Zhou, Xiaohong Xiao, Wei Chen
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2024
Soggetti:	Transfusion
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

Identification of a novel B allele with a c.140_143del on the ABO*B.01 allele
di: Shuang Liang, et al.
Pubblicazione: (2025)

Identification of a novel B allele with c.155+5G>T in the ABO gene associated with Bweak phenotype
di: Yu Zhang, et al.
Pubblicazione: (2025)

Identification of a novel nonsense variant ( c.184C>T ) in ABO*B.01 allele
di: Xiaoyun Bu, et al.
Pubblicazione: (2026)

Identification of a novel A allele with a c. 610G >A variation on the ABO*A1.02 allele
di: Qian Chen, et al.
Pubblicazione: (2026)

Identification of a novel c.77T>G mutation on the ABO*B.01 allele associated with a B subtype
di: Xiao Hao, et al.
Pubblicazione: (2024)

Novel ABO*B allele (c. 701C >T) on ABO*B.01 in a Chinese B(A) phenotype individual
di: Lina Shi, et al.
Pubblicazione: (2026)

A novel variant c.505C>T based on the ABO*B.01 allele associated with a Bel phenotype
di: Hua Wang, et al.
Pubblicazione: (2024)

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype
di: Haixiao Zheng, et al.
Pubblicazione: (2024)

Identification of a novel null allele A4GALT*02: c.457_463dup in one Chinese pedigree with the rare p phenotype and anti‐ PP1P k
di: Yuelin Jin, et al.
Pubblicazione: (2025)

A novel B group allele with a c. 745C >T substitution previously found in ABO*A3.07 subgroup allele
di: Ying Liu, et al.
Pubblicazione: (2025)

Identification of a novel RHAG allele with a c.500A>G variation associated with Rhmod phenotype
di: Xiaozhen Hong, et al.
Pubblicazione: (2025)

Identification of five novel ABO blood group alleles
di: Rahel Kräuchi, et al.
Pubblicazione: (2025)

Characterization of a novel ABO allele with variant c. 575T >C on an A1 .01.02 background
di: Hongli Guan, et al.
Pubblicazione: (2025)

Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)
di: Jue Hou, et al.
Pubblicazione: (2026)

Identification of a novel c.506A>C variant on the ABO*A1.02 allele in a Chinese individual
di: Yongkui Kong, et al.
Pubblicazione: (2024)

A novel c.29‐3C>G variant on the B allele forms the Bel phenotype
di: Yongkui Kong, et al.
Pubblicazione: (2024)

Identification of a novel RHD*01W allele with c.175G>T on the RHD*weak partial 15 allele background
di: Xu Zhang, et al.
Pubblicazione: (2026)

Four novel ABO*B alleles associated with reduced B antigen expression
di: Yan Li, et al.
Pubblicazione: (2024)

Identification of a novel Bw allele with c.810C > G missense variation in a Cambodian‐origin family
di: Shaoyun Wu, et al.
Pubblicazione: (2025)

A novel intronic variant ABO * AW allele resulting in weak A expression
di: Yujung Jung, et al.
Pubblicazione: (2026)

Serological and genetic analysis of a B3 phenotype caused by c.259G > T in the ABO gene
di: Min Zhang, et al.
Pubblicazione: (2025)

A rare ABO allele confers cisAB phenotype
di: Yuli Zhu, et al.
Pubblicazione: (2026)

ABO*cisAB allele with unusual phenotype in a Brazilian family
di: Marcos Paulo Miola, et al.
Pubblicazione: (2024)

Identification of a novel nonfunctional variant, c. 931G >C, on the FUT1*01.02 allele in a Chinese para‐Bombay phenotype individual
di: Qian Su, et al.
Pubblicazione: (2025)

Identification of a novel DEL allele with c.411G>C on the RHD*01EL.01 allele background
di: Lin‐Nan Shao, et al.
Pubblicazione: (2024)

PacBio third‐generation sequencing detects a new variant, c.27delC, in exon 1 of the ABO gene resulting in a weak B phenotype
di: L. Shao, et al.
Pubblicazione: (2024)

A novel RHD allele combining partial D (c. 455A >C) and weak D (c. 1154G >C) variants
di: Glenn Ramsey, et al.
Pubblicazione: (2025)

A novel RHD allele caused by the c.1142G>A mutation identified in a serologic Del phenotype in a Chinese Han male donor
di: Xiao Hao, et al.
Pubblicazione: (2025)

A serologic weak D caused by a novel RHD allele with single nucleotide c. 209G >C variation predicted to encode p. Arg70Pro
di: Evelyne Heng, et al.
Pubblicazione: (2025)

Identification of a novel RHD*404T allele in a Chinese individual with variant D phenotype
di: Yuanyuan Luo, et al.
Pubblicazione: (2025)

Identification of a novel nonfunctional FUT1 allele with 358delC in a Chinese para‐Bombay phenotype individual
di: Xiaobi Tang, et al.
Pubblicazione: (2025)

Identification of two novel variants, c.–35A>T and c.[–35A>T, 725T>G], in the FUT1 gene in a patient exhibiting the para‐Bombay phenotype
di: Kamphon Intharanut, et al.
Pubblicazione: (2024)

Two novel mutations ( c.878T>C and c.1316delA ) in CD36 alleles lead to CD36 antigen deficiency
di: Honghong He, et al.
Pubblicazione: (2025)

New RHCE * cE allele with c. 872C >G and variable RH3 and RH4 phenotypes, predicted to encode p. Pro291Arg
di: Evelyne Heng, et al.
Pubblicazione: (2026)

Identification of a novel A allele with a c.374 + 3_374 + 6delAAGT splicing variant in a Chinese individual
di: Meifang Lan, et al.
Pubblicazione: (2026)

A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual
di: Hongjuan Lyu, et al.
Pubblicazione: (2024)

Novel RHCE * cE ( 341A ) allele
di: Rébecca Voreux, et al.
Pubblicazione: (2026)

Two novel variant allele of the RHD gene detected in two Chinese blood donors with the RHD negative phenotype
di: Qiuhong Mo, et al.
Pubblicazione: (2025)

Identification and analysis of a novel FUT1 allele in Chinese voluntary blood donor
di: Jian‐Cheng Liu, et al.
Pubblicazione: (2026)

Identification of a novel variant (c.1‐111A>G) located in GATA‐1 motif of RHCE proximal promoter in two Chinese patients with the rare D‐‐ phenotype
di: Ran Zhang, et al.
Pubblicazione: (2025)