These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

142 related items for PubMed ID: 22048715

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Common polymorphism rs11191548 near the CYP17A1 gene is associated with hypertension and systolic blood pressure in the Han Chinese population.
    Li X, Ling Y, Lu D, Lu Z, Liu Y, Chen H, Gao X.
    Am J Hypertens; 2013 Apr; 26(4):465-72. PubMed ID: 23467202
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Association of common variants in/near six genes (ATP2B1, CSK, MTHFR, CYP17A1, STK39 and FGF5) with blood pressure/hypertension risk in Chinese children.
    Xi B, Shen Y, Zhao X, Chandak GR, Cheng H, Hou D, Li Y, Ott J, Zhang Y, Wang X, Mi J.
    J Hum Hypertens; 2014 Jan; 28(1):32-6. PubMed ID: 23759979
    [Abstract] [Full Text] [Related]

  • 6. Common variant rs11191548 near the CYP17A1 gene is associated with hypertension and the serum 25(OH) D levels in Han Chinese.
    Zhang N, Jia J, Ding Q, Chen H, Ye X, Ding H, Zhan Y.
    J Hum Genet; 2018 Jun; 63(6):731-737. PubMed ID: 29556032
    [Abstract] [Full Text] [Related]

  • 7. A Single Nucleotide Polymorphism near the CYP17A1 Gene Is Associated with Left Ventricular Mass in Hypertensive Patients under Pharmacotherapy.
    Huber M, Lezius S, Reibis R, Treszl A, Kujawinska D, Jakob S, Wegscheider K, Völler H, Kreutz R.
    Int J Mol Sci; 2015 Jul 30; 16(8):17456-68. PubMed ID: 26263970
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women.
    Hotta K, Kitamoto A, Kitamoto T, Mizusawa S, Teranishi H, Matsuo T, Nakata Y, Hyogo H, Ochi H, Nakamura T, Kamohara S, Miyatake N, Kotani K, Komatsu R, Itoh N, Mineo I, Wada J, Yoneda M, Nakajima A, Funahashi T, Miyazaki S, Tokunaga K, Masuzaki H, Ueno T, Chayama K, Hamaguchi K, Yamada K, Hanafusa T, Oikawa S, Yoshimatsu H, Sakata T, Tanaka K, Matsuzawa Y, Nakao K, Sekine A.
    J Hum Genet; 2012 Jan 30; 57(1):46-51. PubMed ID: 22071413
    [Abstract] [Full Text] [Related]

  • 13. Relationship between CYP17A1 genetic polymorphism and coronary artery disease in a Chinese Han population.
    Dai CF, Xie X, Yang YN, Li XM, Zheng YY, Fu ZY, Liu F, Chen BD, Gai MT, Ma YT.
    Lipids Health Dis; 2015 Mar 07; 14():16. PubMed ID: 25889125
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
    Robiou-du-Pont S, Anand SS, Morrison KM, McDonald SD, Atkinson SA, Teo KK, Meyre D.
    PLoS One; 2017 Mar 07; 12(10):e0186218. PubMed ID: 29045471
    [Abstract] [Full Text] [Related]

  • 16. A new risk locus in CHCHD5 for hypertension and obesity in a Chinese child population: a cohort study.
    Wu L, Gao L, Zhao X, Zhang M, Wu J, Mi J.
    BMJ Open; 2017 Sep 11; 7(9):e016241. PubMed ID: 28893745
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.