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Int J Fertil Steril. 2022 Jan;16(1):36-41.

Article

Association of rs13429458 and rs12478601 Single Nucleotide Polymorphisms of THADA Gene with Polycystic Ovary Syndrome

Leila Naserpoor, Rahil Jannatifar, Kambiz Roshanaei, Mohadeseh Khoshandam, Naser Kallhor

2022

Cell J. 2022 Apr;24(4):163-169.

Article

Methylation and Expression Status of The CpG-Island of SMG1 Promoter in Acute Myeloid Leukemia: A Follow-Up Study in Patients

Neda Karami, Mohammad Hossein Ahmadi, Saeed Mohammadi, Amirhosein Maali, Ahad Alizadeh, S Haghayegh Pishkhan Dibazar, Mehdi Azad

2022

Acta Parasitol. 2022 Mar;67(1):72-78.

Article

Molecular Evidence and Hematological Profile of Bovines Naturally Infected with Ehrlichiosis in Southern Punjab, Pakistan

Muhammad Abdul Basit, Muhammad Ijaz, Jawaria Ali Khan, Kamran Ashraf, Rao Zahid Abbas

2022

J Cell Mol Med. 2021 Oct;25(20):9627-9633.

Article

The association between fat mass and obesity-associated (FTO) genotype and serum vitamin D level in breast cancer patients

Maryam Gholamalizadeh, Zohreh Mokhtari, Saeid Doaei, Vahideh Jalili, Sayed Hossein Davoodi, Mona Jonoush, Mohammad Esmail Akbari, Azadeh Hajipour, Bojlul Bahar, Ghasem Azizi Tabesh, Saeed Omidi, Seyed Alireza Mosavi Jarrahi

2021

Clin Nutr. 2021 Feb;40(2):488-495.

Study

The interaction between the dietary inflammatory index and MC4R gene variants on cardiovascular risk factors

Habib Yarizadeh, Atieh Mirzababaei, Nasim Ghodoosi, Sara Pooyan, Kurosh Djafarian, Cain C T Clark, Khadijeh Mirzaei

2021

J Hum Genet. 2021 Oct;66(10):973-981.

Article

Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature

Mehdi Khorrami, Mohammad Amin Tabatabaiefar, Erfan Khorram, Omid Yaghini, Mojgan Rezaei, Arash Hejazifar, Maryam Riahinezhad, Majid Kheirollahi

2021

Front Physiol. 2021 Feb 26:12:637306.

Article

Identification of Copy Number Variation Among Nonsyndromic Cleft Lip and or Without Cleft Palate With Hypodontia: A Genome-Wide Association Study

Norliana Ghazali, Normastura Abd Rahman, Azlina Ahmad, Sarina Sulong, Thirumulu Ponnuraj Kannan

2021

Arch Razi Inst. 2021 Nov 30;76(5):1551-1554.

Article

Evaluation of the Association of Transferrin Receptor Type 2 Gene Mutation (Y250X) with Iron Overload in Major β- Thalassemia

J Abdulmalek Jaafar, N A M Al-Rashedi

2021

Allergy Asthma Clin Immunol. 2021 Oct 11;17(1):107.

Article

X-linked SCID with a rare mutation

Fatemeh Sadat Mahdavi, Mohammad Keramatipour, Sarina Ansari, Samin Sharafian, Arezou Karamzade, Marzieh Tavakol

2021

Mol Vis. 2021 Sep 2:27:555-563.

Article

Novel mutations of the PAX6, FOXC1, and PITX2 genes cause abnormal development of the iris in Vietnamese individuals

Ha Hai Nguyen, Chau Minh Pham, Hoa Thi Thanh Nguyen, Nhung Phuong Vu, Trang Thu Duong, Ton Dang Nguyen, Bac Duy Nguyen, Hiep Van Nguyen, Hai Van Nong

2021