- Established Type 2 Diabetes-Susceptibility Genetic Variants in Saudi ethnicity: A Mini-Systematic Review
Khalid Siddiqui, Mohthash Musambil, Adnan Mahmood Usmani
JBCGenetics. 2018; 1(2): 57-65
» Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1540811228
- Morphometry and expression of immunoglobulins-containing plasma cells in the Harderian glands of Birds
Mir Rubayet Jahan, Md Nabiul Islam, Md Zahirul Islam Khan, Akie Yanai, Koh Shinoda
J Adv Biotechnol Exp Ther. 2018; 1(2): 55-60
» Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d10
- Dysmorphic features as an early presentation of rare sex chromosome aneuploidies
Salma Hussain Almohammed, Abdul azeem Al-Ibraheem, Yassin Mahmoud Alsaleh, Majed Jawad Al-Buali
JBCGenetics. 2018; 1(2): 53-56
» Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1542546893
- Genomics in Saudi Arabia Call for Data-Sharing Policy
Ahmed Alfares,
JBCGenetics. 2018; 1(2): 51-52
» Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1546945268
- Antibacterial and cytotoxic activity of seeds of white hyacinth bean ( Lablab purpureus L. sweet white )
Sheikh Ashikur Rahman, Md Shamim Akhter
J Adv Biotechnol Exp Ther. 2018; 1(2): 49-54
» Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d9
- Expression patterns of the phosphoproteins and total proteins in TLQP-21 (a VGF derived peptide) treated SH-SY5Y cells
Md Shamim Akhter, Jesus Rodriguez Requena
J Adv Biotechnol Exp Ther. 2018; 1(2): 43-48
» Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d8
- Isolation of stem cell populations from whartons jelly sections of umbilical cord and comparison analysis with cord blood stem cells
Mahaboob Vali Shaik , Hymavathi K, Subrahmanyam G
J Adv Biotechnol Exp Ther. 2018; 1(2): 36-42
» Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d7
- Long term administration of gentamicin affects hemato-biochemical parameters and liver architecture of Swiss albino mice
Nure Jannat, Tanjina Amin, Nasrin Sultana, Mir Rubayet Jahan, Md Rafiqul Islam
J Adv Biotechnol Exp Ther. 2018; 1(2): 29-34
» Abstract » Full-text PDF » doi: 10.5455/jabet.2018.d6
- Epileptic encephalopathy caused by biallelic mutation in PPM1D: a case report
Hind AlMaghthawi, Marwan Nashabat, Majid Alfadhel
JBCGenetics. 2018; 1(1): 47-50
» Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1532438227
- An atypical presentation of severe congenital contractures and lack of cerebellar involvement in a patient with a novel LAMA1 mutation
Ameur Ammari, Amal Alhashem, Hanen Abdelraouf, Fatma Alzahrani, Fowzan Sami Alkuraya, Brahim Tabarki
JBCGenetics. 2018; 1(1): 43-46
» Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1531458597
- An Anxious Day
Amber Zohaib Jafferi
SAJEM. 2018; 1(1): 43-43
» Abstract » Full-text PDF
- The S1Q3T3 Pattern
Madiha Ghazanfar
SAJEM. 2018; 1(1): 42-42
» Abstract » Full-text PDF
- Unusual Epiphyseal Fracture
Shazia Naqvi
SAJEM. 2018; 1(1): 41-41
» Abstract » Full-text PDF
- Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
Maram Alojair, Abdulaziz Alghamdi, Kalthoum Tlili, Sateesh Maddirevula, Fowzan Sami Alkuraya, Brahim Tabarki
JBCGenetics. 2018; 1(1): 40-42
» Abstract » Full-text PDF » doi: 10.24911/JBCGenetics/183-1531469195
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