Keyword Connections

mutations

Journals

16

1 PloS one

2 International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

3 BioMed research international

4 Journal of global antimicrobial resistance

5 Frontiers in bioengineering and biotechnology

6 virus research

7 Journal of computational biology : a journal of computational molecular cell biology

8 best practice & research clinical obstetrics & gynaecology

9 molecular vision

10 clinical and experimental dermatology

11 journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

12 global health, science and practice

13 journal of pediatric endocrinology & metabolism : jpem

14 antiviral chemistry & chemotherapy

15 international journal of hematology

16 blood cancer journal

Research Groups

0

No Research Group Connected

Bibliographies

331

1 Mutational profiling in myelofibrosis: implications for management.

2 Myelofibrosis in 2019: moving beyond JAK2 inhibition.

3 Latent TB Infection (LTBI) - Mycobacterium tuberculosis pathogenesis and the dynamics of the granuloma battleground.

4 Extra-pulmonary tuberculosis: A retrospective study of patients in Accra, Ghana.

5 Incidence of CXCR4 tropism and CCR5-tropic resistance in treatment-experienced participants receiving maraviroc in the 48-week MOTIVATE 1 and 2 trials.

6 Relevance of Ebola virus VP35 homo-dimerization on the type I interferon cascade inhibition.

7 Disease severity of respiratory syncytial virus (RSV) infection correlate to a novel set of five amino acid substitutions in the RSV attachment glycoprotein (G) in China.

8 Structural Dynamics Behind Clinical Mutants of PncA-Asp12Ala, Pro54Leu, and His57Pro of Associated With Pyrazinamide Resistance.

9 Effects of a Peer-Led Intervention on HIV Care Continuum Outcomes Among Contacts of Children, Adolescents, and Young Adults Living With HIV in Zimbabwe.

10 multiple tumor induction after treatment of temporal arteritis with prednisone

11 merokok dan oksidasi dna

12 alterações moleculares associadas à hemocromatose hereditária molecular changes associated with hereditary hemochromatosis

13 new challenges in targeting signaling pathways in acute lymphoblastic leukemia by ngs approaches: an update

14 editorial: physiology and pathophysiology of the extracellular calcium-sensing receptor

15 met and small-cell lung cancer

16 mutations in the quinolone resistance-determining regions of gyra and parc in enterobacteriaceae isolates from brazil

17 genetic testing for cystic fibrosis in adult patients

18 testicular germ cell tumors: molecular genetic and clinicomorphological aspects

19 origin of cancer: an information, energy and matter disease

20 human immunodeficiency virus type-2-a milder, kinder virus: an update

21 ethyl methane sulfonate induced mutations in m2 generation and physiological variations in m1 generation of peppers (capsicum annuum l.)

22 insights of crosstalk between p53 protein and the mkk3/mkk6/p38 mapk signaling pathway in cancer

23 Molecular modeling studies demonstrate key mutations that could affect the ligand recognition by influenza AH1N1 neuraminidase

24 Evaluation of genetic mutations associated with phenotypic resistance to Fluoroquinolones, Bedaquiline, and Linezolid in clinical Mycobacterium tuberculosis: A systematic review and meta-analysis.

25 Novel mutations associated with inherited human calcium-sensing receptor disorders: a clinical genetic study.

26 PRISMOID: a comprehensive 3D structure database for post-translational modifications and mutations with functional impact.

27 Varying inocula permutations (Aspergillus oryzae and bacillus amyloliquefaciens) affect enzyme activities and metabolite levels in koji

28 The creation and selection of mutations resistant to a gene drive over multiple generations in the malaria mosquito.

29 Frequent mutations in EGFR, KRAS and TP53 genes in human lung cancer tumors detected by ion torrent DNA sequencing.

30 Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.

31 Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

32 Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

33 Mutations in gyrB play an important role in ciprofloxacin-resistant Pseudomonas aeruginosa

34 Characterization of hepatitis C virus resistance to grazoprevir reveals complex patterns of mutations following on-treatment breakthrough that are not observed at relapse

35 Patterns of emergent resistance-associated mutations after initiation of non-nucleoside reverse-transcriptase inhibitor-containing antiretroviral regimens in Taiwan: a multicenter cohort study

36 The clinical significance of silent mutations with respect to ciprofloxacin resistance in MRSA

37 Interaction between rpsL and gyrA mutations affects the fitness and dual resistance of Mycobacterium tuberculosis clinical isolates against streptomycin and fluoroquinolones

38 Mutations in the gyrA, parC, and mexR genes provide functional insights into the fluoroquinolone-resistant Pseudomonas aeruginosa isolated in Vietnam

39 Enriched whole genome sequencing identified compensatory mutations in the RNA polymerase gene of rifampicin-resistant Mycobacterium leprae strains

40 Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

41 Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study

42 Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B

43 Mycoplasma genitalium infection: current treatment options, therapeutic failure, and resistance-associated mutations

44 Acute Myeloid Leukemia with Concomitant BCR-ABL and NPM1 Mutations

45 Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

46 Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

47 Mutations in gyrB play an important role in ciprofloxacin-resistant Pseudomonas aeruginosa

48 Characterization of hepatitis C virus resistance to grazoprevir reveals complex patterns of mutations following on-treatment breakthrough that are not observed at relapse

49 Patterns of emergent resistance-associated mutations after initiation of non-nucleoside reverse-transcriptase inhibitor-containing antiretroviral regimens in Taiwan: a multicenter cohort study

50 The clinical significance of silent mutations with respect to ciprofloxacin resistance in MRSA

51 Interaction between rpsL and gyrA mutations affects the fitness and dual resistance of Mycobacterium tuberculosis clinical isolates against streptomycin and fluoroquinolones

52 Mutations in the gyrA, parC, and mexR genes provide functional insights into the fluoroquinolone-resistant Pseudomonas aeruginosa isolated in Vietnam

53 Enriched whole genome sequencing identified compensatory mutations in the RNA polymerase gene of rifampicin-resistant Mycobacterium leprae strains

54 Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

55 Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study

56 Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B

57 Mycoplasma genitalium infection: current treatment options, therapeutic failure, and resistance-associated mutations

58 Proof of Principle that Molecular Modeling Followed by a Biophysical Experiment Can Develop Small Molecules that Restore Function to the Cardiac Thin Filament in the Presence of Cardiomyopathic Mutations.

59 Detection of genetic mutations associated with macrolide resistance of Mycoplasma pneumoniae

60 Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

61 Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

62 Where phonology meets morphology in the context of rapid language change and universal bilingualism: Irish initial mutations in child language

63 Conformational Dynamics and Allosteric Regulation Landscapes of Germline PTEN Mutations Associated with Autism Compared to Those Associated with Cancer

64 Single amino acid mutations in the S. cerevisiae rhomboid peptidase, Pcp1p, alter mitochondrial morphology.

65 Osteopetrotic induced pluripotent stem cells derived from patients with different disease-associated mutations by non-integrating reprogramming methods.

66 Human Hyperekplexic Mutations in Glycine Receptors Disinhibit the Brainstem by Hijacking GABA Receptors.

67 Novel high-capacity robust and imperceptible image steganography scheme using multi-flipped permutations and frequency entropy matching method

68 Novel mutations of the POLR3A gene caused POLR3-related leukodystrophy in a Chinese family: a case report.

69 Novel ALMS1 mutations in Chinese patients with Alström syndrome.

70 [Research progression of LDLR mutations in Chinese Familial hypercholesterolemia].

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

72 Long-Term Follow-Up of Retinal Degenerations Associated With Mutations and Their Comparability to Phenotypes Associated With Mutations.

73 Mutations in Coagulation Factor VIII Are Associated with More Favorable Outcome in Patients with Cutaneous Melanoma

74 Development of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion Mutations

75 Mutations in sigma 70 transcription factor improves expression of functional eukaryotic membrane proteins in Escherichia coli

76 Frequency and patterns of second-line resistance conferring mutations among MDR-TB isolates resistant to a second-line drug from eSwatini, Somalia and Uganda (2014-2016).

77 Allele specific repair of splicing mutations in cystic fibrosis through AsCas12a genome editing

78 Mycobacterium tuberculosis whole genome sequencing provides insights into the Manila strain and drug-resistance mutations in the Philippines.

79 Spontaneous mutations of the Zpld1 gene in mice cause semicircular canal dysfunction but do not impair gravity receptor or hearing functions.

80 Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

81 Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

82 Expanding the clinical spectrum of mutations.

83 Improvement in detecting cytomegalovirus drug resistance mutations in solid organ transplant recipients with suspected resistance using next generation sequencing.

84 Glaucoma-Associated Mutations in the Optineurin Gene Have Limited Impact on Parkin-Dependent Mitophagy.

85 Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome.

86 An unprecedented COPA gene mutation in two patients in the same family: comparative clinical analysis of newly reported patients with other known COPA gene mutations.

87 Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2

88 Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

89 Transhumance et gestion des ressources naturelles au Sahel : contraintes et perspectives face aux mutations des systèmes de productions pastorales

90 A Multi-Center Study of and Germline Mutations in Mexican-Mestizo Breast Cancer Families Reveals Mutations Unreported in Latin American Population.

91 Mutations in the dimer interfaces of the dengue virus capsid protein affect structural stability and impair RNA-capsid interaction

92 Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3.

93 Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome.

94 Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3

95 FORMAL AND SIGNIFICANT MUTATIONS OF TRADITIONAL DIPLOMACY

96 Clinical and genetic spectrum of interstitial lung disease in Chinese children associated with surfactant protein C mutations.

97 Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand.

98 Genetics of hereditary hearing loss in east Iran population: A systematic review of mutations.

99 [Concurrent CALR and SF3B1 gene mutations in a patient with myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis].

100 ENAM mutations and digenic inheritance.

101 Dimerization defective MODY mutations of hepatocyte nuclear factor 4α.