9 The search for plasmodium falciparum histidine-rich protein 2/3 deletions in Zambia and implications for plasmodium falciparum histidine-rich protein 2-based rapid diagnostic tests

10 Identification and Mapping of a 2,009-bp DNA Deletion in SERPING1 of a Hereditary Angioedema Patient

11 SHOX Duplication and Tall Stature in a Patient with Xq Deletion and Vascular Disease

12 Advanced imaging parameters improve the prediction of diffuse lower-grade gliomas subtype, IDH mutant with no 1p19q codeletion: added value to the T2/FLAIR mismatch sign.

13 Xq22 deletions and correlation with distinct neurological disease traits in females: further evidence for a contiguous gene syndrome.

14 CB2 receptor deletion on myeloid cells enhanced mechanical allodynia in a mouse model of neuropathic pain

15 Corpus evidence of anti-deletion in Black South African english noun phrases

16 Anti-deletions in an L2 grammar: A study of black south african english mesolect

17 Detection of a novel large deletion causing α-thalassemia in South China.

18 High-resolution melting analysis of the three common nondeletional α-thalassemia mutations in the Chinese population: Hbs Constant Spring, Quong Sze and Westmead.

19 Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.

20 Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting

21 Correction to: New traits in crops produced by genome editing techniques based on deletions (Plant Biotechnology Reports, (2017), 11, 1, (1-8), 10.1007/s11816-017-0425-z)

22 Identifying the Impact of Inframe Insertions and Deletions on Protein Function in Cancer.

23 Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions.

24 Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.

25 Deletion detection method using the distribution of insert size and a precise alignment strategy.

26 Deletion of Runx2 in condylar chondrocytes disrupts TMJ tissue homeostasis

27 Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion

28 A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature.

29 CRISPR/Cas9-mediated simultaneous knockout of Dmrt1 and Dmrt3 does not recapitulate the 46,XY gonadal dysgenesis observed in 9p24.3 deletion patients.

30 High Frequency Spontaneous Deletions within the IcaADBC Operon of Clinical Staphylococcus epidermidis Isolates.

31 Efficiently Hiding Sensitive Itemsets with Transaction Deletion Based on Genetic Algorithms

32 Impact of leptin deficiency compared to neuronal specific leptin receptor deletion on cardiometabolic regulation.

33 Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion.

34 Systems Network Genomic Analysis Reveals Cardioprotective Effect of MURC/Cavin-4 Deletion Against Ischemia/Reperfusion Injury.

35 Structural characterization of EGFR exon 19 deletion mutation using molecular dynamics simulation.

36 Predicting the 1p/19q co-deletion status of presumed low grade glioma with an externally validated machine learning algorithm.

37 Unusual Form of Obstructive Hydrocephalus in Association with 6q Terminal Deletion Syndrome: A Case Report and Literature Review.

38 Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations

39 Break-induced replication plays a prominent role in long-range repeat-mediated deletion.

40 Frequency of heterozygous TET2 deletions in myeloproliferative neoplasms

41 Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss.

42 The impact of concomitant cytogenetic abnormalities on acute myeloid leukemia with monosomy 7 or deletion 7q after HLA-matched allogeneic stem cell transplantation.

43 Primary ciliary dyskinesia caused by a large homozygous deletion including exons 1-4 of DRC1 in Japanese patients with recurrent sinopulmonary infection.

44 68 CCR2 Deletion Ameloriates Ileal Inflammation, Limits Dysbiosis, and Prevents Invasion by Adherent and Invasive E. coli (AIEC) in Toxoplasma gondii Infected Mice

45 Mapping the Fungal Battlefield: Using Chemistry and Deletion Mutants to Monitor Interspecific Chemical Interactions Between Fungi.

46 Assessing the developmental trajectory of mouse models of neurodevelopmental disorders: Social and communication deficits in mice with Neurexin 1α deletion.

47 Selective deletion of ENTPD1/CD39 in macrophages exacerbates biliary fibrosis in a mouse model of sclerosing cholangitis

48 Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

49 Tricellulin expression and its deletion effects in the endolymphatic sac

50 Deletion of Tricellulin Causes Progressive Hearing Loss Associated with Degeneration of Cochlear Hair Cells

51 Combined deletions of and cause chondrodystrophy and embryonic lethality in the Creeper chicken.

52 Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion.

53 Attenuated SARS-CoV-2 variants with deletions at the S1/S2 junction

54 Connexin 43 deletion in astrocytes promotes CNS remyelination by modulating local inflammation.

55 QualitySNP: a pipeline for detecting single nucleotide polymorphisms and insertions/deletions in EST data from diploid and polyploid species

56 DMD genomic deletions characterize a subset of progressive/higher-grade meningiomas with poor outcome

57 Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study

58 Invasive Infections with Haemophilus influenzae Serotype a Containing an IS1016-bexA Partial Deletion: Possible Association with Virulence

59 QualitySNP: a pipeline for detecting single nucleotide polymorphisms and insertions/deletions in EST data from diploid and polyploid species

60 TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions

61 ABL1 deletion without BCR/ABL1 rearrangement is originated from a large-sized 9q deletion

62 QualitySNP: a pipeline for detecting single nucleotide polymorphisms and insertions/deletions in EST data from diploid and polyploid species

63 2q37 deletion syndrome confirmed by high-resolution cytogenetic analysis

64 generation and characterization of a human induced pluripotent stem (ips) cell line derived from an acute myeloid leukemia patient evolving from primary myelofibrosis carrying the calr 52 bp deletion and the asxl1 p.r693x mutation

65 molecular and cellular pathways associated with chromosome 1p deletions during colon carcinogenesis

66 corrigendum to “first contiguous gene deletion causing biotinidase deficiency: the enzyme deficiency in three sri lankan children” [mol. genet. metab. rep. 2 (2016) 81–84]

67 na+ dependent acid-base transporters in the choroid plexus; insights from slc4 and slc9 gene deletion studies

68 pregnancy with de novo 9q34.3 microdeletion and kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result

69 the ace gene insertion/deletion polymorphism and cerebrovascular diseases in uzbek patients with arterial hypertension

70 12q14 microdeletions: additional case series with confirmation of a macrocephaly region

71 deletions of chromosome 1p and 15q are associated with aggressiveness of gastrointestinal stromal tumors

72 new insight into pathogenicity and secondary metabolism of the plant pathogen penicillium expansum through deletion of the epigenetic reader sntb

73 child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations

74 partial deletion of chromosome 8 β-defensin cluster confers sperm dysfunction and infertility in male mice.

75 construction and characterization of a glycoprotein e deletion mutant of bovine herpesvirus type 1.2 strain isolated in brazil construção e caracterização de uma amostra de bohv-1.2 isolada no brasil com uma deleção no gene da glicoproteína e

76 prenatal diagnosis of cystic hygroma related to a deletion of 16q24.1 with haploinsufficiency of foxf1 and foxc2 genes

77 somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men

78 ptpn11 deletion in cd4+ cells does not affect t cell development and functions but causes cartilage tumors in a t cell-independent manner

79 universal insertion/deletion-enrich pcr

80 stress and final /n/ deletion in catalan: combining strict cv and ot

81 mirna-mediated risk for schizophrenia in 22q11.2 deletion syndrome

82 impaired glucose metabolism and exercise capacity with muscle-specific glycogen synthase 1 (gys1) deletion in adult mice

83 gap-pcr screening for common large deletional mutations of β-globin gene cluster revealed a higher prevalence of the turkish inversion/deletion (δβ)0 mutation in antalya

84 a mammary-specific, long-range deletion on mouse chromosome 11 accelerates brca1-associated mammary tumorigenesis

85 the deletion polymorphism in exon 8 of uncoupling protein 2 is associated with severe obesity in a saudi arabian case–control study

86 patients with high-grade gliomas harboring deletions of chromosomes 9p and 10q benefit from temozolomide treatment

87 detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with wolf–hirschhorn syndrome

88 complex iii deficiency due to an in-frame mt-cyb deletion presenting as ketotic hypoglycemia and lactic acidosis

89 deletion of histone deacetylase 3 in adult beta cells improves glucose tolerance via increased insulin secretion

90 deletion of aif1 but not of yca1/mca1 protects saccharomyces cerevisiae and candida albicans cells from caspofungin-induced programmed cell death

91 congenital arthrogryposis: an extension of the 15q11.2 bp1-bp2 microdeletion syndrome?

92 mitochondrial ferritin deletion exacerbates β-amyloid-induced neurotoxicity in mice

93 fbxw7 deletion accelerates krasg12d-driven pancreatic tumorigenesis via yap accumulation

94 evolution of the insertion-deletion mutation rate across the tree of life

95 delineation of 2q32q35 deletion phenotypes: two apparent “proximal” and “distal” syndromes

96 mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-mb deletion of 21q21.1–q21.2 and 5-mb deletion of 21q22.3

97 high resolution melting curve method for detection of bim deletion

98 aryl hydrocarbon receptor deficiency in an exon 3 deletion mouse model promotes hematopoietic stem cell proliferation and impacts endosteal niche cells

99 a novel assay for detecting the mutation of nucleotide 1758-1777 deletion in core promoter region of hepatitis b virus

100 deletion designs

101 angiotensin converting enzyme gene insertion/deletion polymorphism in migraine patients

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