Back to search

Rhmod Syndrome: A Family Study of the Translation-Initiator Mutation in the Rh50 Glycoprotein Gene

Data up to Jan 2025

Published1999
Citations33
References47

Total Citations Per Year

Abstract

References (47)

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

1979 • 54,907 citations

Short-Term Effects of Nose-Only Cigarette Smoke Exposure on Glutathione Redox Homeostasis, Cytochrome P450 1A1/2 and Respiratory Enzyme Activities in Mice Tissues

2013 • 47,043 citations

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1987 • 5,139 citations

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer.

1988 • 4,669 citations

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1990 • 1,756 citations

Blood groups in man

1962 • 1,174 citations

共やくエクイン・エストロゲン(Premarin)服用閉経婦人の血清エクイリン,エストロン,エストラジオール値

1980 • 725 citations

Decreased Resistance to Bacterial Infection and Granulocyte Defects in IAP-Deficient Mice

1996 • 599 citations

[49] DNA analysis in the diagnosis of hemoglobin disorders

1981 • 338 citations

Molecular cloning and protein structure of a human blood group Rh polypeptide.

1990 • 317 citations

Molecular cloning and primary structure of the human blood group RhD polypeptide.

1992 • 312 citations

The Structure and Insertion of Integral Proteins in Membranes

1990 • 304 citations

cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression

1990 • 275 citations

Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing.

1995 • 243 citations

Molecular cloning of RhD cDNA derived from a gene present in RhD- positive, but not RhD-negative individuals

1993 • 205 citations

Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency

1996 • 158 citations

Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression

1992 • 137 citations

Topology and organization of human Rh (rhesus) blood group-related polypeptides.

1994 • 129 citations

Molecular biology of the Rh antigens

1991 • 126 citations

A SAMPLE OF BLOOD WITH NO DETECTABLE Rh ANTIGENS

1961 • 116 citations

Molecular insights into the Rh protein family and associated antigens

1997 • 114 citations

Molecular biology of the Rh antigens

1991 • 110 citations

4 Biochemical aspects of the blood group Rh (Rhesus) antigens

1993 • 100 citations

Evolution of the Human RH (Rhesus) Blood Group Genes: A 50 Year Old Prediction (Partially) Fulfilled

1997 • 94 citations

The Human Rh50 Glycoprotein Gene

1998 • 81 citations

The β- and δ-Thalassemia Repository (Eighth Edition)

1995 • 80 citations

Alteration of RH gene structure and expression in human dCCee and DCW- red blood cells: phenotypic homozygosity versus genotypic heterozygosity

1996 • 80 citations

Molecular Defects of the RHCE Gene in Rh-Deficient Individuals of the Amorph Type

1998 • 62 citations

Hematological aspect of Rh deficiency syndrome: A case report and a review of the literature

1987 • 61 citations

Murine monoclonal antibody MB‐2D10 recognizes Rh‐related glycoproteins in the human red cell membrane

1990 • 60 citations

Rhnull Disease: The Amorph Type Results From a Novel Double Mutation in RhCe Gene on D-Negative Background

1998 • 59 citations

Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene.

1992 • 51 citations

A Novel Single Missense Mutation Identified Along the RH50 Gene in a Composite Heterozygous Rhnull Blood Donor of the Regulator Type

1998 • 47 citations

An unlinked modifier of Rh blood groups: effects when heterozygous and when homozygous.

1972 • 42 citations

A human monoclonal anti‐D antibody which detects a nonconformation‐dependent epitope on the RhD protein by immunoblot

1997 • 40 citations

Characterization of the gene encoding the human LW blood group protein in LW+ and LW- phenotypes

1996 • 38 citations

Regulator Genes Affecting Red Cell Antigens

1990 • 35 citations

Molecular definition of red cell Rh haplotypes by tightly linked SphI RFLPs.

1996 • 34 citations

Rh50 Glycoprotein Gene and Rhnull Disease: A Silent Splice Donor Is trans to a Gly279→Glu Missense Mutation in the Conserved Transmembrane Segment

1998 • 32 citations

Rhmod, a Second Kindred (Craig)1

1976 • 23 citations

A splicing mutation of the RHAG gene associated with the Rhnull phenotype

1998 • 21 citations

RH Blood Groups and Rh-Deficiency Syndrome

1995 • 21 citations

Identification of 5′ Flanking Sequence ofRH50Gene and the Core Region for Erythroid-Specific Expression

1998 • 19 citations

Strength of translation initiation signal sequence of mRNA as studied by quantification method: effect of nucleotide substitutions upon translation efficiency in rat preproinsulin mRNA

1996 • 18 citations

β-Spectrin Promissão: A Translation Initiation Codon Mutation of the β-Spectrin Gene (ATG → GTG) Associated With Hereditary Spherocytosis and Spectrin Deficiency in a Brazilian Family

1998 • 15 citations

β-Spectrin Promissão: A Translation Initiation Codon Mutation of the β-Spectrin Gene (ATG → GTG) Associated With Hereditary Spherocytosis and Spectrin Deficiency in a Brazilian Family

1998 • 14 citations

1 Biochemistry and molecular genetics of Rh antigens

1991 • 8 citations

Cited By (0)

Loading...
Rhmod Syndrome: A Family Study of the Translation-Initiator Mutation in the Rh50… (1999) – The American Journal of Human Genetics | Metascience Observatory Explorer