Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hilal Unsal"'
Autor:
Elif Soyak Aytekin, Umit M. Sahiner, Sevda Tuten Dal, Hilal Unsal, Ozan Hakverdi, Berna Oguz, Yasemin Ozsurekci, Bulent E. Sekerel, Ozge Soyer
Publikováno v:
Pediatric Pulmonology. 57:1668-1676
It is not clear whether asthma, the most frequent chronic disease in childhood, is a risk for severe SARS-CoV-2 infection in the pediatric population and how SARS-CoV-2 infection affects the lung functions in these patients.We aimed to investigate th
Publikováno v:
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and ImmunologyREFERENCES. 33(4)
Legumes are nutritionally valuable as an inexpensive protein source, but may cause severe allergic reactions. This study aimed to identify the characteristics of legume allergies (LAs) in Turkish children.A total of 87 children (4.9 (3.1-7.0) years)
Autor:
Emine Polat, Fatma Zehra Öztek Çelebi, Melahat Melek Oguz, Saliha Senel, Husniye Yucel, Esma Altinel Acoglu, Gürses Şahin, Hilal Unsal, Meltem Akcaboy, Eyup Sari
Publikováno v:
Pediatric Hematology and Oncology. 36:1-16
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening syndrome of excessive immune activation. Secondary HLH syndrome develops as a complication of infection, drugs, rheumatologic conditions, or malignancy. The main objectives of this work w
Publikováno v:
Journal of Biological Chemistry. 273:9510-9516
Intestinal expression of the high affinity Na+/glucose cotransporter 1 (SGLT1), which absorbs dietary glucose and galactose, exhibits both circadian periodicity in its activity and induction by dietary carbohydrate. Because the daily variation in SGL
Autor:
Michael Krainer, Kanamaru R, Kurt J. Isselbacher, Daniel A. Haber, Chikashi Ishioka, Michael G. FitzGerald, Akira Shimada, Anne M. Bowcock, Sandra Silva-Arrieta, Hilal Unsal, Dianne M. Finkelstein, Deborah J. MacDonald
Publikováno v:
New England Journal of Medicine. 336:1416-1422
Background Germ-line mutations in the BRCA1 and BRCA2 genes predispose women to breast cancer. BRCA1 mutations are found in approximately 12 percent of women with breast cancer of early onset, and the specific mutation causing a deletion of adenine a
Autor:
Daniel A. Haber, Kathleen A. Mayzel, Peggy Beer-Romero, Dianne M. Finkelstein, Erin O'Neil, Michael Krainer, Kurt J. Isselbacher, Jerry Younger, Stephen H. Friend, Christoph Englert, Hilal Unsal, Dennis C. Sgroi, Rosemary B. Duda, Barbara L. Smith, Michael G. FitzGerald, Deborah J. MacDonald, Ingrid Hoover, Sandra Silva-Arrieto, Judy Garber
Publikováno v:
New England Journal of Medicine. 334:143-149
Background Mutations in a germ-line allele of the BRCA1 gene contribute to the familial breast cancer syndrome. However, the prevalence of these mutations is unknown in women with breast cancer who do not have the features of this familial syndrome.
Autor:
Christophe Marcais, Hans Zentgraf, Hilal Unsal, Cengiz Yakicier, Kurt J. Isselbacher, Martin Volkmann, Michael Kew, Mehmet Ozturk
Publikováno v:
Proceedings of the National Academy of Sciences. 91:822-826
We studied 80 hepatocellular carcinomas from three continents for p53 gene (TP53) mutations and hepatitis B virus (HBV) sequences. p53 mutations were frequent in tumors from Mozambique but not in tumors from South Africa, China, and Germany. Independ
Autor:
Daniel A. Haber, Jonathan F. Bean, Dianne M. Finkelstein, Deborah J. MacDonald, D P Harkin, S R Hegde, Michael G. FitzGerald, Kurt J. Isselbacher, Hilal Unsal
Publikováno v:
Nature genetics. 15(3)
Ataxia telangiectasia (AT) is a recessive syndrome, including cerebellar degeneration, immunologic defects and cancer predisposition, attributed to mutations in the recently isolated ATM (ataxia telangiectasia, mutated) gene. AT is diagnosed in 1/40,