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  1. 221
    “…These transcripts are named TcKnk3-Full Length (TcKnk3-FL), TcKnk3-5′ and TcKnk3-3′. All three Knk-family genes appear to have essential and non-redundant functions. …”
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    Functional Specialization Among Members Of Knickkopf Family Of Proteins In Insect Cuticle Organization
  2. 222
    “…High levels of expression of all three PIM family members were observed in both noninvasive and invasive urothelial carcinomas. …”
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    A Small-Molecule Inhibitor of PIM Kinases as a Potential Treatment for Urothelial Carcinomas()()
  3. 223
    “…Sequencing with gene-specific primers confirmed that the changes—rs2330991, c.433 C>T (p.R145W); rs2330992, c.440A>G (p.Q147R); and rs4049504, c.449C>T (p.T150M)—present in all ten affected family members are located in CRYBB2 and are not artifacts of cross-reaction with CRYBB2P1. …”
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    Congenital cataracts: de novo gene conversion event in CRYBB2
  4. 224
    “…SETTING: A tertiary centre for neuromuscular diseases in England. PATIENTS: All boys without family history diagnosed with DMD in the last 10 years (n=20). …”
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    Improving recognition of Duchenne muscular dystrophy: a retrospective case note review
  5. 225
    “…It is important that providers give a clear recommendation to screen regardless of the test ultimately selected and should advise all patients that family history and the absence of symptoms or colitis do not eliminate the value of screening. …”
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    Identifying key variables in African American adherence to colorectal cancer screening: the application of data mining
  6. 226
    por Hirsh, Vera
    Publicado 2015
    “…The activity of afatinib in both first-line and relapsed/refractory settings may reflect its ability to irreversibly inhibit all ErbB family members. Afatinib has a well-defined safety profile with characteristic gastrointestinal (diarrhea, stomatitis) and cutaneous (rash/acne) adverse events.…”
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    Next-Generation Covalent Irreversible Kinase Inhibitors in NSCLC: Focus on Afatinib
  7. 227
    “…Candidate mutations and cosegregation of the phenotype were verified by polymerase chain reaction and Sanger sequencing in all of the family members. RESULTS: We identified a novel TMC1 mutation in exon 20, c.1979C>T, p.P660L, which segregated with prelingual autosomal recessive sensorineural hearing loss. …”
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    Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss
  8. 228
    “…Genetic analysis of the index patient’s pedigree revealed that the mutation was present in all seven affected family members available, but absent in the 13 unaffected family members examined. …”
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    A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis
  9. 229
    “…Further investigation showed that expression divergence played important roles in gene survival after expansion. All of these family genes were expressed in most of developmental stages and tissues in rice plants. …”
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    Expansion Mechanisms and Evolutionary History on Genes Encoding DNA Glycosylases and Their Involvement in Stress and Hormone Signaling
  10. 230
    “…Through analysis of tumor methylomes, we discovered TET1 as a methylated target, and further confirmed its frequent downregulation/methylation in cell lines and primary tumors of multiple carcinomas and lymphomas, including nasopharyngeal, esophageal, gastric, colorectal, renal, breast and cervical carcinomas, as well as non-Hodgkin, Hodgkin and nasal natural killer/T-cell lymphomas, although all three TET family genes are ubiquitously expressed in normal tissues. …”
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    Epigenetic inactivation of the CpG demethylase TET1 as a DNA methylation feedback loop in human cancers
  11. 231
    “…CONCLUSION: Relationships with health providers, informational support, and continuity in case management all influence the family caregiving experience and ultimately the quality of care for the stroke survivor, during the transition home from a rehabilitation facility. …”
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    Using a complex adaptive system lens to understand family caregiving experiences navigating the stroke rehabilitation system
  12. 232
    “…In the family with the DCTN2 variant, exome sequencing was then carried out on all available eight family members to rule out the presence of more potential variants. …”
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    Variants in the genes DCTN2,DNAH10,LRIG3, and MYO1A are associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family
  13. 233
    “…CASE PRESENTATION: We reported an isolated PJS patient who died of colon cancer, whose blood sample was collected together with all the available family members’. The entire coding region of the STK11 gene was amplified by PCR and analyzed by Sanger sequencing, through which, a novel mutation, c.962_963delCC in exon 8 was identified in this patient. …”
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    Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient
  14. 234
    “…Compared to other professional groups, psychiatric nurses reported lower scores on almost all aspects of family-focused practice except supporting clients in their parenting role within the context of their mental illness. …”
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    Mental health professionals’ family-focused practice with families with dependent children: a survey study
  15. 235
    “…The monophyly of Pleuronectoidei, which comprises all but one family of flatfishes, is broadly supported. …”
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    Flatfish monophyly refereed by the relationship of Psettodes in Carangimorphariae
  16. 236
    “…Next generation sequencing (NGS) with a multiple gene panel including MMR genes showed a germline mutation in MLH1 (c.1852_1854delAAG, p.K618del) in all 3 affected family members and confirmed the diagnosis of Lynch syndrome. …”
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    A Chinese family affected by lynch syndrome caused by MLH1 mutation
  17. 237
    “…The redundancy encourages inhibition of more than one cytokine or one of the shared receptors. All IL-20 family members utilize the Janus kinase signaling pathway and are therefore potentially inhibited by drugs targeting these enzymes. …”
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    The IL-20 Cytokine Family in Rheumatoid Arthritis and Spondyloarthritis
  18. 238
    “…We then examined the effects of deleting all ARI1 family members in the nematode Caenorhabditis elegans, which to our knowledge represents the first complete knockout of ARI1 function in a metazoan. …”
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    Regulation of germ cell development by ARI1 family ubiquitin ligases in C. elegans
  19. 239
    “…PURPOSE: Herein, we assessed the expression of all SLIT–ROBO family in bone marrow (BM) biopsy of AML patients and control group on both protein and RNA levels. …”
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    The Expression of the SLIT–ROBO Family in Adult Patients with Acute Myeloid Leukemia
  20. 240
    “…Saudi Arabia as suggested by various studies put more of its attention at all levels to family medicine in order to produce an adequate number of family physicians and improve both the academic aspects and the services provided by family medicine in the country. …”
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    Family Medicine Research Productivity in Saudi Arabia for 15 Years: An Urgent Call for Action
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