PubMed Central (PMC3 - NLM DTD)
Mostrando recursos 101 - 120 de 679
Cell cycle and centromere FISH studies in premature centromere division
- Corona-Rivera, Alfredo; Salamanca-Gomez, Fabio; Bobadilla-Morales, Lucina; Corona-Rivera, Jorge R; Palomino-Cueva, Cesar; Garcia-Cobian, Teresa A; Corona-Rivera, Enrique
Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD)
- Arning, Larissa; Kraus, Peter H; Saft, Carsten; Andrich, Jürgen; Epplen, Jörg T
Sequence diversity within the HA-1 gene as detected by melting temperature assay without oligonucleotide probes
- Graziano, Claudio; Giorgi, Massimo; Malentacchi, Cecilia; Mattiuz, Pier Luigi; Porfirio, Berardino
Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease
- Hoffjan, Sabine; Stemmler, Susanne; Parwez, Qumar; Petrasch-Parwez, Elisabeth; Arinir, Umut; Rohde, Gernot; Reinitz-Rademacher, Karin; Schultze-Werninghaus, Gerhard; Bufe, Albrecht; Epplen, Jörg T
Estrogen receptor alpha dinucleotide repeat polymorphism in Japanese patients with autoimmune thyroid diseases
- Ban, Yoshiyuki; Taniyama, Matsuo; Tozaki, Teruaki; Tomita, Motowo; Ban, Yoshio
Lack of association between estrogen receptor β dinucleotide repeat polymorphism and autoimmune thyroid diseases in Japanese patients
- Ban, Yoshiyuki; Tozaki, Teruaki; Taniyama, Matsuo; Tomita, Motowo; Ban, Yoshio
The vitamin D receptor polymorphism in the translation initiation codon is a risk factor for insulin resistance in glucose tolerant Caucasians
- Chiu, Ken C; Chuang, Lee-Ming; Yoon, Carol
Change of dopamine receptor mRNA expression in lymphocyte of schizophrenic patients
- Kwak, Yong T; Koo, Min-Seong; Choi, Chul-Hee; Sunwoo, IN
Polymorphisms in the Mn-SOD and EC-SOD Genes and Their Relationship to Diabetic Neuropathy in Type 1 Diabetes Mellitus
- Chistyakov, Dimitry A; Savost'anov, Kirill V; Zotova, Elena V; Nosikov, Valery V
Genetic studies of the Roma (Gypsies): a review
- Kalaydjieva, Luba; Gresham, David; Calafell, Francesc
Platelet count and Interleukin 6 Gene polymorphism in healthy subjects
- Fernandez-Real, José-Manuel; Vendrell, Joan; Richart, Cristobal; Gutierrez, Cristina; Ricart, Wifredo
Vitamin D receptor initiation codon polymorphism influences genetic susceptibility to type 1 diabetes mellitus in the Japanese population
- Ban, Yoshiyuki; Taniyama, Matsuo; Yanagawa, Tatsuo; Yamada, Satoru; Maruyama, Taro; Kasuga, Akira; Ban, Yoshio
Apolipoprotein E gene polymorphism is not a strong risk factor for diabetic nephropathy and retinopathy in Type I diabetes: case-control study
- Shcherbak, Natalia S
ApoE polymorphisms in narcolepsy
- Gencik, Martin; Dahmen, Norbert; Wieczorek, Stefan; Kasten, Meike; Gencikova, Alexandra; Epplen, Jorg T
Lamin A/C truncation in dilated cardiomyopathy with conduction disease
- MacLeod, Heather M; Culley, Mary R; Huber, Jill M; McNally, Elizabeth M
The G-308A variant of the Tumor Necrosis Factor-α (TNF-α) gene is not associated with obesity, insulin resistance and body fat distribution
- Romeo, Stefano; Sentinelli, Federica; Capici, Francesca; Arca, Marcello; Berni, Andrea; Vecci, Elio; Di Mario, Umberto; Baroni, Marco Giorgio
Multi-exon deletions of the FBN1 gene in Marfan syndrome
- Liu, Wanguo; Schrijver, Iris; Brenn, Thomas; Furthmayr, Heinz; Francke, Uta
Linkage analysis of HLA and candidate genes for celiac disease in a North American family-based study
- Neuhausen, Susan L; Feolo, Michael; Farnham, James; Book, Linda; Zone, John J
A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
- Rosch, Raphael; Klinge, Uwe; Si, Zhongyi; Junge, Karsten; Klosterhalfen, Bernd; Schumpelick, Volker
The Siblings With Ischemic Stroke Study (SWISS) Protocol
- Meschia, James F; Brown, Robert D; Brott, Thomas G; Chukwudelunzu, Felix E; Hardy, John; Rich, Stephen S
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