Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

A Novel Intronic Splicing Mutation in the EXT2 Gene of a Chinese Family with Multiple Osteochondroma.

  • Authors : Guo X; Department of Laboratory Medicine, Fuzhou Second Hospital Affiliated to Xiamen University, Fuzhou, P.R. China.; Chen S

Subjects: Exostoses, Multiple Hereditary/Exostoses, Multiple Hereditary/Exostoses, Multiple Hereditary/*genetics ; N-Acetylglucosaminyltransferases/N-Acetylglucosaminyltransferases/N-Acetylglucosaminyltransferases/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jul; Vol. 25 (7), pp. 478-485.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

Record details

×
Academic Journal

The CYP19A1 rs700519 Polymorphism and Breast Cancer Susceptibility in China: A Case-Control Study and Updated Meta-Analysis.

  • Authors : Lv F; Department of Oncology and Shengjing Hospital of China Medical University, Shenyang, China.; Huang W

Subjects: Aromatase/Aromatase/Aromatase/*genetics ; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jul; Vol. 25 (7), pp. 486-495.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

Record details

×
Academic Journal

Association Between TPM1 Gene Polymorphisms and Idiopathic Congenital Talipes Equinovarus Risk in a Chinese Population.

  • Authors : Li J; Department of Paediatric Orthopaedics, Guangzhou Women and Children's Medical Centre, Guangzhou Medical University, Guangzhou, China.; Zhu G

Subjects: Clubfoot/Clubfoot/Clubfoot/*genetics ; Tropomyosin/Tropomyosin/Tropomyosin/*genetics; Alleles

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 May; Vol. 25 (5), pp. 355-360. Date of Electronic Publication: 2021 May 04.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

Record details

×
Academic Journal

Evaluation of the Genetic Association and Methylation of Immune Response Pathway Genes with the Risk of Chronic Periodontitis in the Uighur Population.

  • Authors : Abasijiang A; Department of Endodontics, First Affiliated Hospital of Xinjiang Medical University, and College of Stomatology of Xinjiang Medical University, Urumqi, China.; Lin J

Subjects: Chronic Periodontitis/Chronic Periodontitis/Chronic Periodontitis/*genetics ; Receptors, Formyl Peptide/Receptors, Formyl Peptide/Receptors, Formyl Peptide/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 May; Vol. 25 (5), pp. 317-324. Date of Electronic Publication: 2021 May 04.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

Record details

×
Academic Journal

Association of Transforming Growth Factor β1 Gene Polymorphisms and Inflammatory Factor Levels with Susceptibility to Sepsis.

  • Authors : Zheng R; Department of Respiratory and Critical Care Medicine, Ningbo Yinzhou People's Hospital, Ningbo, China.; Fu Z

Subjects: Sepsis/Sepsis/Sepsis/*genetics ; Transforming Growth Factor beta1/Transforming Growth Factor beta1/Transforming Growth Factor beta1/*genetics ; Transforming Growth Factor beta1/Transforming Growth Factor beta1/Transforming Growth Factor beta1/*metabolism

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Mar; Vol. 25 (3), pp. 187-198.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

Record details

×
Academic Journal

Identification of Novel Mutations in the EXT1 and EXT2 Genes of Chinese Patients with Hereditary Multiple Osteochondromas.

  • Authors : Tong Y; The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.; Zhang Y

Subjects: Exostoses, Multiple Hereditary/Exostoses, Multiple Hereditary/Exostoses, Multiple Hereditary/*genetics ; N-Acetylglucosaminyltransferases/N-Acetylglucosaminyltransferases/N-Acetylglucosaminyltransferases/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Feb; Vol. 25 (2), pp. 145-151.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

Record details

×
Academic Journal

Relationship Between the ApoE Gene Polymorphism and Type 2 Diabetes Mellitus Complications.

  • Authors : Gao C; Cadre Ward-2, Fourth Medical Center of General Hospital of PLA, Beijing, China.; Fu X

Subjects: Apolipoproteins E/Apolipoproteins E/Apolipoproteins E/*genetics ; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*complications ; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Feb; Vol. 25 (2), pp. 111-115.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

Record details

×
Academic Journal

A Shared Susceptibility Locus in the p53 Gene for both Gastric and Esophageal Cancers in a Northwestern Chinese Population.

  • Authors : Cao J; Key Laboratory of Environmental Health and Chronic Disease Prevention and Control, School of Public Health, Ningxia Medical University, Yinchuan, Ningxia, People's Republic of China.; Chen Z

Subjects: Genes, p53*; Adenocarcinoma/Adenocarcinoma/Adenocarcinoma/*genetics ; Asian People/Asian People/Asian People/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Dec; Vol. 24 (12), pp. 804-811. Date of Electronic Publication: 2020 Dec 07.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

Record details

×
Academic Journal

Variants c.677 C>T, c.1298 A>C in MTHFR , and c.66 A>G in MTRR Affect the Occurrence of Recurrent Pregnancy Loss in Chinese Women.

  • Authors : Zhang Y; Medical Genetics Center, Guangdong Women and Children Hospital, Guangzhou, P.R. China.; Maternal and Children Metabolic-Genetic Disease Key Laboratory of Guangdong Women and Children Hospital, Guangzhou, P.R. China.

Subjects: Abortion, Spontaneous/Abortion, Spontaneous/Abortion, Spontaneous/*genetics ; Ferredoxin-NADP Reductase/Ferredoxin-NADP Reductase/Ferredoxin-NADP Reductase/*genetics ; Methylenetetrahydrofolate Reductase (NADPH2)/Methylenetetrahydrofolate Reductase (NADPH2)/Methylenetetrahydrofolate Reductase (NADPH2)/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Nov; Vol. 24 (11), pp. 717-722. Date of Electronic Publication: 2020 Oct 29.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

Record details

×
Academic Journal

Association of Genetic Variation in a Wnt Signaling Pathway Gene ( β-Catenin ) with Susceptibility to Leukoaraiosis.

  • Authors : Yadav BK; Department of Biochemistry, Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.; Yadav R

Subjects: Leukoaraiosis/Leukoaraiosis/Leukoaraiosis/*genetics ; beta Catenin/beta Catenin/beta Catenin/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Nov; Vol. 24 (11), pp. 708-716. Date of Electronic Publication: 2020 Oct 07.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

Record details

×
  • 1-10 of  93 results for ""Alleles""