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homozygous

Synonyms

Adjective

1. homozygous

Usage
A Novel Homozygous MYH2 Variant Causing Early-Onset External Ophthalmoplegia and Proximal Myopathy in a Consanguineous Family - Cureus
Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource - Nature
Homozygous Achondroplasia With Long-Term Survival: Growth Patterns, Medical Interventions, and Practice Implications - Wiley Online Library
Genetically heterozygous - transcriptionally homozygous IRF7 deficiency underlies herpesvirus CNS infections in humans - Rockefeller University Press
Functional inactivation of MDR3 caused by a homozygous ABCB4 missense variant leading to liver failure - Frontiers
AAV gene therapy for homozygous familial hypercholesterolemia: a phase 1 trial - Nature
Insights from 173,303 Pakistan Genome Analyses - Bioengineer.org
A Novel Homozygous KIF1C Variant in 2 Cases of Spastic Ataxia Type 2 - Neurology® Journals
FDA Approves Lomitapide for Children With Homozygous Familial Hypercholesterolemia - Pharmacy Times
A novel homozygous variant in the ATP7B gene in a patient with Wilson’s disease: a case report - Frontiers
Homozygous CHD8 mutation intensifies ASD phenotypes and attenuates sex differences - Nature
Homozygous DBX1 Nonsense Variant in a Case of Atypical Congenital Central Hypoventilation - Neurology® Journals
A Novel Homozygous SCNN1B Variant Causing Severe Systemic Pseudohypoaldosteronism Type 1B in a Saudi Infant: A Case Report - Cureus
Case Report: Two siblings with a novel homozygous SLC18A2 variant causing parkinsonism-dystonia-2: a case series from Saudi Arabia - Frontiers
A novel homozygous splicing variant in FRA10AC1 : further delineation of the phenotype - Nature
Myocardial Infarction in a Patient With Homozygous Plasminogen Activator Inhibitor-1 (PAI-1) 4G/4G Mutation: A Case Report - Cureus
50 years of apheresis for homozygous familial hypercholesterolemia - Nature
Differential phenotypes in mice with smooth muscle-specific heterozygous versus homozygous deletion of Stk11 - Nature
Juvenile/adult-type galactosialidosis with a homozygous CTSA variant without consanguinity - Nature
Whisking Behaviour Reveals Stronger Evidence of Habituation in Homozygous Reeler Mice Compared to Controls - Wiley Online Library
FDA Expands Indication for Lomitapide to Include Pediatric Patients With Homozygous Familial Hypercholesterolemia - Drug Topics
Functional Analysis of a Homozygous MYBPC3 Null Allele in Human Pediatric Patients - American Heart Association Journals
Risk of Systemic Manifestations in Homozygous Carriers of the Transthyretin V142I Variant: A Million Veteran Program Analysis - American Heart Association Journals
Uneventful pregnancies with homozygous KISS1 frameshift mutation - The Lancet
Infantile-Onset Vanishing White Matter Disease in an Azerbaijani Infant With a Homozygous EIF2B5 p.(Arg195His) Variant - Cureus
Homozygous Variant in NADSYN1 Causes Multiple Congenital Vertebral Malformation, With Neurodevelopmental Disorder - Wiley Online Library
A novel homozygous COX6A1 variant causes axonal charcot-marie-tooth disease, developmental delays and mitochondrial dysfunction - Nature
Case Report: Characterization of a RAC2 R68W Homozygous Activating Mutation Causing Combined Immune Deficiency - Frontiers
A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia - Nature
A homozygous variant in the beta-1,3-N-acetylglucosaminyltransferase 4 gene causes progressive brain atrophy and muscular dystrophy | European Journal of Human Genetics - Nature
Abnormal development of gastrointestinal system of homozygous Foxp2 (R552H)-mutated mice - Nature
Does siRNA therapy against ANGPTL3 bring new hope in homozygous familial hypercholesterolaemia? - The Lancet
Chorea-Acanthocytosis in a Patient With a Novel Homozygous Pathogenic Variant in the VPS13A Gene - Neurology® Journals
Correction to: Evinacumab for Pediatric Patients With Homozygous Familial Hypercholesterolemia | Circulation - American Heart Association Journals
Genetic rescue of Florida panthers reduced homozygosity but did not swamp ancestral genotypes - PNAS
Adult-Onset Nephrotic Syndrome due to a Homozygous TNS2 Truncating Variant: Broadening the Mutational Spectrum - Wiley Online Library
Regeneron’s Evkeeza Approved in U.S. for Young Children with Homozygous Familial Hypercholesterolemia - Pharmaceutical Executive
Adult-Onset Nephrotic Syndrome due to a Homozygous TNS2 Truncating Variant: Broadening the Mutational Spectrum - Wiley Online Library
Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors - Nature
Evinacumab for Homozygous Familial Hypercholesterolemia - National Institutes of Health (.gov)
Evinacumab for Homozygous Familial Hypercholesterolemia - NEJM
Evinacumab for Pediatric Patients With Homozygous Familial Hypercholesterolemia | Circulation - American Heart Association Journals
Neuroaxonal Dystrophy With Osteopetrosis Associated With a Novel Biallelic Nonsense Homozygous Variant in BORCS5 - Wiley Online Library
Efficacy, Safety, and Tolerability of Inclisiran in Patients With Homozygous Familial Hypercholesterolemia: Results From the ORION-5 Randomized Clinical Trial | Circulation - American Heart Association Journals
Association of Homozygous A2 allele of IL-4Gene with Mortality of Spontaneous Intracerebral Hemorrhage Patients - European Open Science
Efficacy and Safety of Inclisiran in Adolescents With Genetically Confirmed Homozygous Familial Hypercholesterolemia: Results From the Double-Blind, Placebo-Controlled Part of the ORION-13 Randomized Trial | Circulation - American Heart Association Journals
Treatment of Homozygous Familial Hypercholesterolemia: - JACC Journals
CCR5 -∆32 is deleterious in the homozygous state in humans - Nature
Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9 - Nature
Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del - NEJM
Novel homozygous ESAM variants in two families with perinatal strokes showing variable neuroradiologic and clinical findings - Nature
Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma - Nature
The homozygous LRRK2.p.N1437D point mutation mouse is a novel model of parkinsonism | npj Parkinson's Disease - Nature
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality - Nature
Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle - Nature
Taking a color photo: A homozygous 25-bp deletion in Bace2 may cause brown-and-white coat color in giant pandas - PNAS
The mutagenic chain reaction: A method for converting heterozygous to homozygous mutations - Science | AAAS
Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR - NEJM
Phenotype in an Infant with SOD1 Homozygous Truncating Mutation - NEJM
Vitamin D–Binding Protein Deficiency and Homozygous Deletion of the GC Gene - NEJM
Rapid generation of homozygous fluorescent knock-in human cells using CRISPR–Cas9 genome editing and validation by automated imaging and digital PCR screening - Nature
Evinacumab and Cardiovascular Outcome in Patients With Homozygous Familial Hypercholesterolemia - American Heart Association Journals
Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome - Nature
Outpatient monthly plasmapheresis with post-PLEX evinacumab in pediatric homozygous familial hypercholesterolemia: a case report on port access and immunoglobulin preservation - Frontiers
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder - Nature
A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis - Nature
Expanding the phenotypic spectrum of CC2D2A -related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis - Nature
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant - Nature
Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population - Nature
Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH Registry - American Heart Association Journals
Essential genes shape cancer genomes through linear limitation of homozygous deletions - Nature
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study - The Lancet
Evolocumab Treatment in Pediatric Patients With Homozygous Familial Hypercholesterolemia: Pooled Data From Three Open-Label Studies | Arteriosclerosis, Thrombosis, and Vascular Biology - American Heart Association Journals
Chromosome level genome assembly and annotation of the Swanson rainbow trout homozygous line - Nature
Efficient generation of mice carrying homozygous double-floxp alleles using the Cas9-Avidin/Biotin-donor DNA system - Nature
Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia - Nature
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene - Nature
KAT6B overexpression rescues embryonic lethality in homozygous null KAT6A mice restoring vitality and normal lifespan - Nature
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme - Nature
A homozygous variant in ARHGAP39 is associated with lethal cerebellar vermis hypoplasia in a consanguineous Saudi family - Nature
Long-term course of a case with a novel homozygous kyphoscoliosis peptidase variant - Nature
Evinacumab Approval Adds a New Option for Homozygous Familial Hypercholesterolemia With a Hefty Price Tag - American Heart Association Journals
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome - Wiley Online Library
Targeting the absence: Homozygous DNA deletions as immutable signposts for cancer therapy - PNAS
A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasia - Nature
A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizures - Nature
Homozygous Familial Hypercholesterolemia: Luck Meets Opportunity Meets Knowledge - JACC Journals
Homozygosity for R47H in TREM2 and the Risk of Alzheimer’s Disease - NEJM
Introducing Personalized Medicine Into Pediatric Homozygous Familial Hypercholesterolemia Care - American Heart Association Journals
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease - Nature
Systematic screens of a Candida albicans homozygous deletion library decouple morphogenetic switching and pathogenicity - Nature
Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families - Nature
Phase 1 Trials of PNPLA3 siRNA in I148M Homozygous Patients with MAFLD - NEJM
Supravalvular Aortic Stenosis in Homozygous Familial Hypercholesterolemia: Contemporary Management - JACC Journals
Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review - Wiley Online Library
Homozygous IL37 mutation associated with infantile inflammatory bowel disease - PNAS
Case Report: A rare homozygous patient affected by TTR systemic amyloidosis with a prominent heart involvement - Frontiers
A homozygous missense variant in the YG box domain in an individual with severe spinal muscular atrophy: a case report and variant characterization - Frontiers
Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy - Nature
Recurrent homozygous deletion of DROSHA and microduplication of PDE4DIP in pineoblastoma - Nature
Foreign Language Equivalents
Foreign Language Equivalents of 'homozygous'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
hoozygous,   homoztgous,   homozgyous,   homozygou,   homozugous,   homzoygous,   hommozygous,   hoomozygous,   gomozygous,   hoomzygous,   homozygus,   homozgous,   himozygous,   homozygosu,   homozygius,   homozyogus,   hmozygous,   homizygous,   homozyygous,   ho,ozygous,   homozyguos,   homozygoua,   hpmozygous,   homozygouss,   honozygous,   homozyhous,   hmoozygous,   ohmozygous,   homozygpus,   jomozygous,   homozygos,   homoozygous,   homozygois,   omozygous,   homozygoous,   homozygoud,   homoyzgous,   homozyggous,   homoygous,   hompzygous,   homozyfous,   homozygouus,   homoxygous,   homozzygous,   homozyous,   homzygous,   homozygoys,   hhomozygous
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
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