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KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
Author:
Neubauer, B. A.
;
Waldegger, S.
;
Heinzinger, J.
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 03 (Jul. 2008)
, page 177-183
Lymphocyte gene expression in subjects fed a low-choline diet differs between those who develop organ dysfunction and those who do not
Author:
Niculescu, Mihai D.
;
Kerry-Ann da Costa
;
Fischer, Leslie M
;
Zeisel, Steven H.
Artikel dari
The American Journal of Clinical Nutrition vol. 86 no. 01 (Jul. 2007)
, page 230
Markedly elevated plasma myeloperoxidase protein in patients with pelvic inflammatory disease who have A allele myeloperoxidase gene polymorphism
Author:
Shun-An, Lee
;
Po-Hui, Wang
;
Hui-Ling, Chiou
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 93 no. 04 (Mar. 2010)
, page 1260-1266,
No association of the Arg51Gln and Leu72Met polymorphisms of the ghrelin gene and polycystic ovary syndrome
Author:
Kehua, Wang
;
Leiguang, Wang
;
Yueran, Zhao
;
Yuhua, Shi
;
Laicheng, Wang
;
Zi-Jiang Chen
Artikel dari
Human Reproduction vol. 24 no. 02 (Feb. 2009)
, page 485
No evidence of somatic DNA copy number alterations in eutopic and ectopic endometrial tissue in endometriosis
Author:
Saare, M.
;
Soritsa, D.
;
Vaidla, K.
;
Palta, P.
Artikel dari
Human Reproduction vol. 27 no. 06 (Jun. 2012)
, page 1857-1864
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
Author:
Lin C.H.
;
Tan, E.K.
;
Chen, M.L.
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 21 (Nov. 2008)
, page 1727-1732
Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1
Author:
Stamm, D. S.
;
Powell, C. M.
;
Stajich, J. M.
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 22 (Nov. 2008)
, page 1764-1769
Ovarian cancer-associated polymorphisms in the BNC2 gene among women with endometriosis
Author:
Sundqvist, J.
;
Falconer, H.
;
Seddighzadeh, M.
;
Vodolazkaia, A.
;
Fassbender, A.
;
Kyama, C. M.
;
Bokor, A.
;
Stephansson, O.
;
Gemzell-Danielsson, K.
;
D'Hooghe, T.M.
Artikel dari
Human Reproduction vol. 26 no. 08 (Aug. 2011)
, page 2253-2257
Platelet aggregation abnormalities in patients with fetal losses: the GP6 gene polymorphism
Author:
Sokol, Juraj
;
Biringer, Kamil
;
Skerenova, Maria
;
Hasko, Miroslav
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 98 no. 05 (Nov. 2012)
, page 1170-1174
Premutation allele pool in myotonic dystrophy type 2
Author:
Bachinski, L. L.
;
Czernuszewicz, T.
;
Ramagli, L. S.
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 72 no. 06 (Feb. 2009)
, page 490-497
Quantitative trait analysis suggests polymorphisms of estrogen-related genes regulate human sperm concentrations and motility
Author:
I.-Wen, Lee
;
Po-Hsiu, Kuo
;
Mei-Tsz, Su
;
Long-Ching, Kuan
;
Chao-Chin, Hsu
;
Pao-Lin, Kuo
Artikel dari
Human Reproduction vol. 26 no. 06 (Jun. 2011)
, page 1585-1596
Replication of endometriosis-associated single-nucleotide polymorphisms from genome-wide association studies in a Caucasian population
Author:
Sundqvist, J.
;
Xu, H.
;
Vodolazkaia, A.
;
Fassbender, A.
;
Kyama, C.M.
;
Bokor, A.
Artikel dari
Human Reproduction vol. 28 no. 03 (Mar. 2013)
, page 835-839
Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study
Author:
Carty, C.L.
;
Spencer, K.L.
;
Setiawan, V.W.
;
Fernandez-Rhodes, L.
;
Malinowski, J.
Artikel dari
Human Reproduction vol. 28 no. 06 (Jun. 2013)
, page 1695-1706
Risk alleles for multiple sclerosis in multiplex families
Author:
D’Netto, M. J.
;
Ward, H.
;
Morrison, K. M.
Artikel dari
Neurology (Official Journal of The American Academy of Neurology) vol. 72 no. 23 (Jun. 2009)
, page 1984-1988
rs189037, a functional variant in ATM gene promoter, is associated with idiopathic nonobstructive azoospermia
Author:
Li, Zhongxiang
;
Yu, Jianmin
;
Tao Zhang
;
Li, Hongchao
;
Ni, Ya
Artikel dari
Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 100 no. 06 (Dec. 2013)
, page 1536-1541
Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers
Author:
Tan, Y.-Q.
;
Tan, K.
;
Zhang, S.-P.
;
Gong, F.
;
Cheng, D.-H.
Artikel dari
Human Reproduction vol. 28 no. 09 (Sep. 2013)
, page 2581-2592
Testing Multiple Levels of Influence in the Intergenerational Transmission of Alcohol Disorders From a Developmental Perspective: The Example of Alcohol Use Promoting Peers and µ-opioid Receptor M1 Variation
Author:
Chassin, Laurie
;
Lee, Matthew R.
;
Cho, Young Il
;
Wang, Frances L.
;
Agrawal, Arpana
;
Sher, Kenneth J.
;
Lynskey, Michael T.
Artikel dari
Development and Psychopathology vol. 24 no. 3 (Aug. 2012)
, page 953-967
The CETP TaqIB Polymorphism Is Associated With the Risk of Sudden Death in Type 2 Diabetic Patients
Author:
Porchay-Balderelli, Isabelle
;
Pean, Franck
;
Bellili, Naima
;
Jaziri, Riphed
;
and Others
Artikel dari
Diabetes Care vol. 30 no. 11 (Nov. 2007)
, page 2863
Variation of the Transcription Factor 7-Like 2 (TCF7L2) Gene Predicts Impaired Fasting Glucose in Healthy Young Adults
Author:
Raitakari, Olli T.
;
Ronnemma, Tapani
;
Huupponen, Risto
;
Viikari, Liisa
;
Meng, Fan
;
and Others
Artikel dari
Diabetes Care vol. 30 no. 09 (Sep. 2007)
, page 2299
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