Zobrazeno 1 - 10
of 19
pro vyhledávání: '"D J, Zand"'
Publikováno v:
Clinical genetics. 88(6)
Noonan syndrome (NS) and related disorders, such as NS with multiple lentigines (formerly called LEOPARD syndrome), cardiofaciocutaneous syndrome, and Costello syndrome, constitute an important group of developmental malformation syndromes with varia
Publikováno v:
Molecular and Cellular Biology. 9:3166-3173
Hemin-induced differentiation of the human erythroleukemia cell line K562 results in the expression and accumulation of erythroid-specific gene products such as embryonic and fetal hemoglobins and the elevated synthesis of the major heat shock protei
Autor:
Ekbote, Archana P.1 (AUTHOR) ekbotearchana@yahoo.com, Ratnaparkhe, Varsha R.2 (AUTHOR) patwadkarvasha@gmail.com
Publikováno v:
IETE Journal of Research. Jan/Feb2022, Vol. 68 Issue 1, p638-644. 7p.
Autor:
Sabahi, Mohammadmahdi, Ahmadi, Sara Ami, Kazemi, Azin, Mehrpooya, Maryam, Khazaei, Mojtaba, Ranjbar, Akram, Mowla, Ashkan
Publikováno v:
Oxidative Medicine & Cellular Longevity; 9/8/2022, p1-11, 11p
Autor:
V. K., Vincy Devi, R., Rajesh
Publikováno v:
International Journal of Electrical & Computer Engineering (2088-8708); Oct2021, Vol. 11 Issue 5, p4281-4288, 8p
Autor:
Kane, Jennifer1, Berrebi, Kristen1, McLean, Riley1, Petkiewicz, Stephanie1,2, Hay, Beverly3, Martin, Madelena3, Wiss, Karen1,3 Karen.Wiss@umassmemorial.org
Publikováno v:
Clinical Case Reports. Jul2017, Vol. 5 Issue 7, p1152-1154. 3p.
Autor:
Gonzalez-Garcia, Juan, Telleria-Orriols, Carlos, Estupinan-Romero, Francisco, Bernal-Delgado, Enrique
Publikováno v:
IEEE Journal of Biomedical & Health Informatics; Sep2020, Vol. 24 Issue 9, p2671-2680, 10p
Autor:
Timmons, Andrew, Fray, Emily, Kumar, Mithra, Fengting Wu, Weiwei Dai, Bullen, Cynthia Korin, Peggy Kim, Hetzel, Carrie, Chao Yang, Subul Beg, Jun Lai, Pomerantz, Joel L., Yukl, Steven A., Siliciano, Janet D., Siliciano, Robert F.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 7/7/2020, Vol. 117 Issue 27, p15763-15771, 9p
Autor:
Thennavan, Aatish1, Narayanaswamy, Venkadasalapathi2, Niazi, Thanvir Mohammed3, Rao, Lakshmi4, Radhakrishnan, Raghu1 raghu.radhakrishnan@gmail.com
Publikováno v:
Case Reports in Pediatrics. 2012, p1-5. 5p.
Autor:
Couser, Natario L., Keelean‐Fuller, Debra, Davenport, Marsha L., Haverfield, Eden, Masood, Maheer M., Henin, Mark, Aylsworth, Arthur S.
Publikováno v:
American Journal of Medical Genetics. Part A; Sep2018, Vol. 176 Issue 9, p2024-2027, 2027p