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1. The overlapping of phenotypes in Wiedemann-Steiner, Kleefstra and Coffin-Siris syndromes: a study of eleven patients.

2. Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor.

3. Growth, body composition, and endocrine-metabolic profiles of individuals with Kleefstra syndrome provide directions for clinical management and translational studies.

4. Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family.

5. Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical Reports

6. A novel 11 base pair deletion in KMT2C resulting in Kleefstra syndrome 2.

7. Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link.

8. Complete trisomy 9 detected by noninvasive prenatal testing and confirmed by amniocentesis.

9. Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis.

10. Acute myeloid leukemia with t(X;6)9p11;q23);MYB-GATA1 and female sex: GATA1 insufficiency may be insufficient for pathogenesis

11. Risk prediction for metastasis of clear cell renal cell carcinoma using digital multiplex ligation‐dependent probe amplification

12. [Genetic analysis of a case with a supernumerary marker derived from chromosome 9]

13. 9p24.1 alterations and programmed cell death 1 ligand 1 expression in early stage unfavourable classical Hodgkin lymphoma: an analysis from the German Hodgkin Study Group NIVAHL trial

14. Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY): Molecular Profiling Confirms Frequent MAPK Pathway Activation

15. Loss of a Premature Stop Codon in the Rice Wall-Associated Kinase 91 ( WAK91 ) Gene Is a Candidate for Improving Leaf Sheath Blight Disease Resistance.

17. Atendimiento odontológico domiciliario en niño con trisomía 9 – en mosaico: reporte de caso

18. Myelodysplastic syndrome with t(6;9)(p22;q34.1)/DEK-NUP214 better classified as acute myeloid leukemia? A multicenter study of 107 cases

19. First episode of psychosis in Kleefstra syndrome: a case report

20. Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype

21. Genetics of symptom remission in outpatients with COVID-19

22. Congenital hydrocephalus in a trisomy 9p gained child:a case report

23. Kallmann syndrome in a patient with Weiss–Kruszka syndrome and a de novo deletion in 9q31.2

24. Loss of 9p21 Regulatory Hub Promotes Kidney Cancer Progression by Upregulating HOXB13

25. Partial Trisomy 9p with Clinical Symptoms Resembling Interferonopathies

26. Loss of SFRP1 expression is a key progression event in gastrointestinal stromal tumor pathogenesis

27. [Familial intestinal degenerative neuropathy with chronic pseudo-obstruction linked to duplication in chromosome 9]

28. Genetic variability in 13q33 and 9q34 is linked to aggressiveness patterns and a higher risk of progression of non‐muscle‐invasive bladder cancer at the time of diagnosis

29. 9p21.3 Coronary Artery Disease Locus Identifies Patients With Treatment Benefit From Bariatric Surgery in the Nonrandomized Prospective Controlled Swedish Obese Subjects Study

30. Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia

31. Allogeneic stem cell transplantation in AML with t(6;9)(p23;q34);DEK-NUP214 shows a favourable outcome when performed in first complete remission

32. Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma

33. Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population

34. The Single Nucleotide Polymorphisms of Chromosome 9p21 and CD147 Were Relevant with the Carotid Plaque Risk in Acute Cerebral Infarction Patients Among Chinese Han Population

35. Case–Control Study on the Interaction Effects of rs10757278 Polymorphisms at 9p21 Locus and Traditional Risk Factors on Coronary Heart Disease in Xinjiang, China

36. Chronic myeloid leukemia: 2020 update on diagnosis, therapy and monitoring

37. Partial trisomy 9p and 14q microduplication in a patient with growth retardation: a case report and review of the literature

38. Hemizygous loss of NF2 detected by fluorescence in situ hybridization is useful for the diagnosis of malignant pleural mesothelioma

39. A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report

40. [Clinical and genetic analysis of three children patients with Kleefstra syndrome]

41. Exploiting the passenger ACO1-deficiency arising from 9p21 deletions to kill T-cell lymphoblastic neoplasia cells

42. Pericentric inversion (Inv) 9 variant—reproductive risk factor or benign finding?

43. CDKN2B gene expression is affected by 9p21.3 rs10757278 in CAD patients, six months after the MI

44. Clinicopathological and molecular genomic features of monomorphic epitheliotropic intestinal T-cell lymphoma in the Chinese population: a study of 20 cases

45. Genetic variants of PON1, GSTM1, GSTT1, and locus 9p21.3, and the risk for premature coronary artery disease in Yucatan, Mexico

46. [Genetic analysis of a family with 9q34.3 microdeletion and microduplication caused by abnormal chromosome balance structure]

47. Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: A large-scale genetic association study

48. Genetic Variants and Somatic Alterations Associated with MITF-E318K Germline Mutation in Melanoma Patients

49. CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency

50. Polymorphic Rearrangements of Human Chromosome 9 and Male Infertility: New Evidence and Impact on Spermatogenesis.

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