Search Results - "Gad, Yehia Z."

Extracellular miR-145, miR-223 and miR-326 expression signature allow for differential diagnosis of immune-mediated neuroinflammatory diseases by Sharaf-Eldin, Wessam E., Kishk, Nirmeen A., Gad, Yehia Z., Hassan, Heba, Ali, Mohamed A.M., Zaki, Maha S., Mohamed, Mohamed R., Essawi, Mona L.

“…Although misdiagnosis of neuromyelitis optica spectrum disorder (NMOSD) with neuropsychiatric systemic lupus erythematosus (NPSLE) or multiple sclerosis (MS)…”
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Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 by Abdel‐Aziz, Nahla, El‐Kamah, Ghada, Khairat, Rabab, Mohamed, Hanan, Gad, Yehia, El‐Ghor, Akmal M., Amr, Khalda S.

“…Background Neurofibromatosis 1 (NF1; OMIM# 162200) is a common autosomal dominant genetic disease [incidence: ~1:3500]. In 95% of cases, clinical diagnosis of…”
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The Egypt Genome Project by Elmonem, Mohamed A., Soliman, Neveen A., Moustafa, Ahmed, Gad, Yehia Z., Hassan, Wael A., Taha, Tarek, El-Feky, Gina, Sakr, Mahmoud, Amer, Khaled

“…The recently launched Egyptian Genome Project aims to sequence genomic variants of 100,000 apparently healthy Egyptian adults, with around 8,000 individuals…”
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Ancestry and Pathology in King Tutankhamun's Family by Hawass, Zahi, Gad, Yehia Z, Ismail, Somaia, Khairat, Rabab, Fathalla, Dina, Hasan, Naglaa, Ahmed, Amal, Elleithy, Hisham, Ball, Markus, Gaballah, Fawzi, Wasef, Sally, Fateen, Mohamed, Amer, Hany, Gostner, Paul, Selim, Ashraf, Zink, Albert, Pusch, Carsten M

“…CONTEXT The New Kingdom in ancient Egypt, comprising the 18th, 19th, and 20th dynasties, spanned the mid-16th to the early 11th centuries BC. The late 18th…”
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Insights from ancient DNA analysis of Egyptian human mummies: clues to disease and kinship by Gad, Yehia Z, Hassan, Naglaa Abu-Mandil, Mousa, Dalia M, Fouad, Fayrouz A, El-Sayed, Safaa G, Abdelazeem, Marwa A, Mahdy, Samah M, Othman, Hend Y, Ibrahim, Dina W, Khairat, Rabab, Ismail, Somaia

“…Abstract The molecular Egyptology field started in the mid-eighties with the first publication on the ancient DNA (aDNA) analysis of an Egyptian mummy. Egypt…”
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Egypt Genome: Towards an African new genomic era by Amer, Khaled, Soliman, Neveen A., Soror, Sameh, Gad, Yehia Z., Moustafa, Ahmed, Elmonem, Mohamed A., Amer, May, Ragheb, Ameera, Kotb, Amira, Taha, Tarek, Ali, Wael, Sakr, Mahmoud, Ghaffar, Khaled Abdel

“…[Display omitted] •Studying human genome is crucial to embrace precision medicine.•The Northern bias in research for the last two decades precluded diversity…”
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Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt by El-Kamah, Ghada Y, Mohamed, Amal M, Gad, Yehia Z, Abdelhak, Sonia, Hennig, Branwen J, Ramesar, Raj S, Landouré, Guida, Gaye, Amadou, Newport, Melanie J, Williams, Scott M, Ramsay, Michèle

“…The tenth conference of the African Society of Human Genetics was held in Egypt with the theme "Human Genetics and Genomics in Africa: Challenges for Both Rare…”
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Biochemical Analysis of Four Missense Mutations in the HSD17B3 Gene Associated With 46,XY Disorders of Sex Development in Egyptian Patients by Engeli, Roger T., Tsachaki, Maria, Hassan, Heba A., Sager, Christoph P., Essawi, Mona L., Gad, Yehia Z., Kamel, Alaa K., Mazen, Inas, Odermatt, Alex

“…Mutations in the HSD17B3 gene are associated with a 46,XY disorder of sexual development (46,XY DSD) as a result of low testosterone production during…”
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First insights into the metagenome of Egyptian mummies using next-generation sequencing by Khairat, Rabab, Ball, Markus, Chang, Chun-Chi Hsieh, Bianucci, Raffaella, Nerlich, Andreas G, Trautmann, Martin, Ismail, Somaia, Shanab, Gamila M. L, Karim, Amr M, Gad, Yehia Z, Pusch, Carsten M

“…We applied, for the first time, next-generation sequencing (NGS) technology on Egyptian mummies. Seven NGS datasets obtained from five randomly selected Third…”
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King Tutankhamun’s Family and Demise—Reply by Gad, Yehia Z, Selim, Ashraf, Pusch, Carsten M

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Molecular analysis of 5α-reductase type 2 gene in eight unrelated egyptian children with suspected 5α-reductase deficiency: prevalence of the G34R mutation by Mazen, Inas, Gad, Yehia Z., Hafez, Mona, Sultan, Charles, Lumbroso, Serge

“…Summary objective Analysis of the 5α‐reductase type 2 (SRD5A2) gene in Egyptian patients with suspected 5α‐reductase (5αR) deficiency. patients and methods…”
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Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study by Hawass, Zahi, Ismail, Somaia, Selim, Ashraf, Saleem, Sahar N, Fathalla, Dina, Wasef, Sally, Gad, Ahmed Z, Saad, Rama, Fares, Suzan, Amer, Hany, Gostner, Paul, Gad, Yehia Z, Pusch, Carsten M, Zink, Albert R

“…Objective To investigate the true character of the harem conspiracy described in the Judicial Papyrus of Turin and determine whether Ramesses III was indeed…”
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A Novel Double Mutation in the Luteinizing Hormone Receptor in a Kindred with Familial Leydig Cell Hypoplasia and Male Pseudohermaphroditism by Pals-Rylaarsdam, Robin, Liu, Guoquan, Brickman, Wendy, Duranteau, Lise, Monroe, Jason, El-Awady, Mostafa K., Gad, Yehia Z., Shenker, Andrew

“…We report a novel mutant of the luteinizing hormone receptor (LHR) in a case of familial Leydig cell hypoplasia and pseudohermaphrotidism. The proband was…”
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Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells by EL-AWADY, Mostafa K, GAD, Yehia Z, YANPING WEN, EASSAWI, Mona, EFFAT, Laila, AMR, Khalda S, ISMAIL, Somaia, CHRIST, George J

“…Bladder carcinoma accounts for 26% of reported human malignancies in Egypt, and has been strongly associated with urinary schistosomiasis. Nevertheless, the…”
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Who killed Ramesses III? by Hawass, Zahi, Ismail, Somaia, Selim, Ashraf, Saleem, Sahar N, Fathalla, Dina, Wasef, Sally, Gad, Ahmed Z, Saad, Rama, Fares, Suzan, Amer, Hany, Gostner, Paul, Gad, Yehia Z, Pusch, Carsten M, Zink, Albert R

“…The end of Ramesses III's life has long been debated among Egyptologists. A series of historical documents, of which the most important is the Judicial Papyrus…”
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Molecular analysis of 5[alpha]-reductase type 2 gene in eight unrelated Egyptian children with suspected 5[alpha]-reductase deficiency: Prevalence of the G34R mutation by Mazen, Inas, Gad, Yehia Z, Hafez, Mona, Sultan, Charles, Lumbroso, Serge

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Molecular analysis of 5alpha-reductase type 2 gene in eight unrelated egyptian children with suspected 5alpha-reductase deficiency: prevalence of the G34R mutation by Mazen, Inas, Gad, Yehia Z, Hafez, Mona, Sultan, Charles, Lumbroso, Serge

“…Analysis of the 5alpha-reductase type 2 (SRD5A2) gene in Egyptian patients with suspected 5alpha-reductase (5alphaR) deficiency. Eight unrelated patients,…”
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The milder phenotype of the dystrophin gene double deletions by El-Harouni, A. A., Amr, K. S., Effat, L. K., Eassawi, M. L., Ismail, S., Gad, Y. Z., El-Awady, M. K.

“…Objectives – This study aimed to examine the genotype–phenotype correlation in Duchenne muscular dystrophy (MD) patients with double deletion (Ddel) mutations…”
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Molecular analysis of androgen resistance syndromes in Egyptian patients by Essawi, M, Gad, Y Z, el-Rouby, O, Temtamy, S A, Sabour, Y A, el-Awady, M K

“…Androgen resistance syndromes [i.e. 5 alpha-reductase deficiency (5 alpha RD) and androgen receptor (AR) defects] are frequently reported among Egyptian…”
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Studies of up-regulation of androgen receptors in genital skin fibroblasts by Gad, Y Z, Berkovitz, G D, Migeon, C J, Brown, T R

“…Prolonged exposure of genital skin fibroblasts (GSF) to dihydrotestosterone (DHT) increases androgen receptor binding of steroid, a process termed…”
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