Search Results - "Medical genetics

Haplotype Analysis in Carriers of β-Globin Gene Mutation Facil-itates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran by Nasrollah SALEH-GOHARI, Kolsoum SAEIDI, Sima ZIAADINI-DASHTKHAKI

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Total fertilization failure with in vitro fertilization-intracytoplasmic sperm injection related to WEE2 mutation highlights emerging importance of genetic causes of in vitro ferti... by Hillary S. Weiner, M.B.E, Nicole D. Ulrich, M.D, Lauren Hipp, M.S., C.G.C, Ahmad Hammoud, M.D, Min Xu, Ph.D, Samantha B. Schon, M.D

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Impacts of BMI & IL-4 Genetic Polymorphisms (rs2243250 C/T & rs2227284 A/C) on Iranian Breast Cancer Patients: a Pilot Study by Samanehsadat Shahidi, Zahra Tahmasebi Fard

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Exploring the genetic differences between primary and metastatic prostate cancer using bioinformatic approaches: a preliminary study / Faris Aizat Ahmad Fajri ... [et al.] by Ahmad Fajri, Faris Aizat, Nazri, Muhammad Amru, Zulkifli, Muhamad Harith, Mohd Fauzi, Fazlin

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Rising Cellular Immune Response after Injection of pVax/iutA: A Genetic DNA Cassette as Candidate Vaccine against Urinary Tract Infection by Ronak BAKHTIARI, Shahin AHMADIAN, Jalil FALLAH MEHRABADI

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Genetic evidence for predisposition to acute leukemias due to a missense mutation (p.Ser518Arg) in ZAP70 kinase: a case-control study by Khalil Khashei Varnamkhasti, Samire Khashei Varnamkhasti, Atefeh Shahrouzian, Masoomeh Rahimzadeh, Leila Naeimi, Behrouz Naeimi, Sirous Naeimi

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Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss by Marjan MASOUDI, Najmeh AHANGARI, Ali Akbar POURSADEGH ZONOUZI, Ahmad POURSADEGH ZONOUZI, Azim NEJATIZADEH

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Genetic Association of UGT1A1 Promoter Variants (c.-3279T>G and c.-3156G>A) with Neonatal Hyperbili-rubinemia in an Iranian Population by Nasim Pouralizadeh, Gholamali Mamouri, Abbas Boskabadi, Hassan Boskabadi, Houshang Rafatpanah, Ali Moradi, Hassan Mehrad-Majd

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Rising Cellular Immune Response after Injection of pVax/iutA: A Genetic DNA Cassette as Candidate Vaccine against Urinary Tract Infection by Ronak BAKHTIARI, Shahin AHMADIAN, Jalil FALLAH MEHRABADI

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Variation in cytokine genes can contribute to severity of acetabular osteolysis and risk for revision in patients with ABG 1 total hip arthroplasty: a genetic association study by Mrazek Frantisek, Gallo Jiri, Petrek Martin

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The <it>INSIG2 </it>rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts by Mosley Thomas H, Dent Robert, McPherson Ruth, Lewis Cora E, Kao Wen, Hanis Craig L, Fornage Myriam, Bressler Jan, Pennacchio Len A, Boerwinkle Eric

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Evaluation of CYP2C19 Genetic Variant and Its Lack of Association with Valproic Acid Plasma Concentrations Among Zhuang and Han Schizophrenia Patients in Guangxi by Teng JM, Qin S, Lu D, Gu Y, Tang SJ, Yan Q, Yao J, Zhang C

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Respuesta autoinmune en pacientes con enfermedades genéticas y desregulación del sistema inmune Autoimmune response in patients with genetic diseases and immune system deregulati... by Bárbara Torres Rives, Goitybell Martínez Téllez, Araceli Lantigua Cruz, Suchiquil Rangel Velázquez, Juana Duany Sánchez, Vicky Sánchez Rodríguez, Lilia Caridad Marín Padrón

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Polimorfismos genéticos do fator de crescimento do endotélio vascular na pré-eclâmpsia Genetic polymorphisms of vascular endothelial growth factor in pre-eclampsia by Valquiria Maria de Paula Cunha, Roseane Lopes da Silva Grecco, Marina Carvalho Paschoini, Sueli Riul da Silva, Mariângela Torreglosa Ruiz, Marly Aparecida Spadotto Balarin

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Cystic Fibrosis Case for First-Year Medical Students - Team-Based Learning Format by Maria Sheakley, Sharma Davendranand, Mary Moore, James Grogan, David Averill

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Medical management of melasma: A review with consensus recommendations by Indian pigmentary expert group by Rashmi Sarkar, Narendra Gokhale, Kiran Godse, Pallavi Ailawadi, Latika Arya, Nilendu Sarma, R G Torsekar, V K Somani, Pooja Arora, Imran Majid, G Ravichandran, Mohan Singh, Sanjeev Aurangabadkar, Shehnaz Arsiwala, Sidharth Sonthalia, T Salim, Swapnil Shah

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Prospects for Expansion of Universal Newborn Screening in Bulgaria: A Survey among Medical Professionals by Georgi Iskrov, Vyara Angelova, Boyan Bochev, Vaska Valchinova, Teodora Gencheva, Desislava Dzhuleva, Julian Dichev, Tanya Nedkova, Mariya Palkova, Anelia Tyutyukova, Maria Hristova, Eleonora Hristova-Atanasova, Rumen Stefanov

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Disentangling the genetics of sarcopenia: prioritization of NUDT3 and KLF5 as genes for lean mass & HLA-DQB1-AS1 for hand grip strength with the associated enhancing SNPs & a scori... by Abhishek Narain Singh, Bili Gasman

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Regulation of drug metabolism and toxicity by multiple factors of genetics, epigenetics, lncRNAs, gut microbiota, and diseases: a meeting report of the 21st International Symposium... by Ai-Ming Yu, Magnus Ingelman-Sundberg, Nathan J. Cherrington, Lauren M. Aleksunes, Ulrich M. Zanger, Wen Xie, Hyunyoung Jeong, Edward M. Morgan, Peter J. Turnbaugh, Curtis D. Klaassen, Aadra P. Bhatt, Matthew R. Redinbo, Pengying Hao, David J. Waxman, Li Wang, Xiao-bo Zhong

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Anhidrotic ectodermal dysplasia-A case series in a medical center in southern Taiwan by Kuei-Chung Liu, Ching-Yuang Huang, Sheau-Chiou Chao

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