848 results on '"P. Propping"'
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2. Correction to: Differences in clinical presentation and management between pre- and postsurgical diagnoses of urinary bladder paraganglioma: is there clinical relevance? A systematic review
3. Contractile responses in intact and mucosa-denuded human ureter—a comparison with urinary bladder detrusor preparations
4. Level of education and mortality after radical prostatectomy
5. Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1
6. Diagnostic and prognostic value of bladder cancer-related transcript markers in urine
7. Lee mortality index as comorbidity measure in patients undergoing radical cystectomy
8. Risk stratification for locoregional recurrence after radical cystectomy for urothelial carcinoma of the bladder
9. Brief Report: No Association between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin
10. A similarity-based method for genome-wide prediction of disease-relevant human genes.
11. Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
12. Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder
13. Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
14. Ziele und Grenzen der Quantifizierung genetischer Risiken
15. Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies
16. The muscarinic receptor antagonist propiverine exhibits α1-adrenoceptor antagonism in human prostate and porcine trigonum
17. Genetische Krebsdiagnostik: Fluch oder Segen für die Patienten?
18. Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder
19. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2
20. Brief Report: No Association Between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin
21. Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder
22. A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
23. Familiärer Darmkrebs
24. Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14
25. Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants
26. Linkage analyses of chromosomal region 18p11-q12 in dyslexia
27. Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin.
28. Systematic investigation of genetic variability in 111 human genes—implications for studying variable drug response
29. Die genetische Revolution: Bedeutung für Therapie und Prävention
30. Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
31. Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers
32. Genetik bipolar affektiver Störungen Gegenwärtiger Stand der Arbeiten zur Identifikation von Dispositionsgenen: Gegenwärtiger Stand der Arbeiten zur Identifikation von Dispositionsgenen
33. A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26
34. Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)
35. Erbliches kolorektales Karzinom: Was kann die molekulargenetische Diagnostik leisten?
36. Dopamine D3 receptor variant and tardive dyskinesia
37. DRD4 exon III VNTR polymorphism—susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach
38. Die genetischen Grundlagen erblicher Tumorkrankheiten des Menschen
39. Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
40. Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers
41. Erblich bedingte gastrointestinale Tumorerkrankungen
42. Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families
43. Gerd Utermann: Ordinarius in Innsbruck 1984–2008
44. Hautkrankheiten und genetische Instabilität Teil II: Genodermatosen mit genetischer Instabilität: Teil II: Genodermatosen mit genetischer Instabilität
45. Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease
46. Hautkrankheiten und genetische Instabilität Teil I: Grundlagen genetischer Instabilität: Teil I: Grundlagen genetischer Instabilität
47. Friedrich Vogel 1925–2006
48. Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia
49. Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
50. Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia
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