Search Results - "Naiman, T"

Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer by ROZEN, P, SHOMRAT, R, STRUL, H, NAIMAN, T, KARMINSKY, N, LEGUM, C, ORR-URTREGER, A

“…Background & Aims: Israeli Jews of European birth, i.e., Ashkenazim, have the highest colorectal cancer incidence of any Israeli ethnic group. The I1307K APC…”
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Molecular Cloning of a Novel Human Gene Encoding a 63-kDa Protein and Its Sublocalization within the 11q13 Locus by Perelman, Boris, Dafni, Naomi, Naiman, Tova, Eli, Dalia, Yaakov, Miri, Feng, Teresa L.Yang, Sinha, Srish, Weber, Günther, Khodaei, Shideh, Sancar, Aziz, Dotan, Iris, Canaani, Dan

“…A human cDNA previously isolated by virtue of its ability to complement partially the ultraviolet sensitivity of a xeroderma pigmentosum cell line was further…”
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Complementation of the UV-Sensitive Phenotype of a Xeroderma Pigmentosum Human Cell Line by Transfection with a cDNA Clone Library by Teitz, Tal, Naiman, Tova, Avissar, Sofia S., Bar, Sara, Okayama, Hiroto, Canaani, Dan

“…In previous work, a xeroderma pigmentosum cell line belonging to complementation group C was established by transformation with origin-defective simian virus…”
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Ultraviolet light-resistant primary transfectants of xeroderma pigmentosum cells are also DNA repair-proficient by Stark, M, Naiman, T, Canaani, D

“…In a previous work, an immortal xeroderma pigmentosum cell line belonging to complementation group C was complemented to a UV-resistant phenotype by…”
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The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families by Geva, E, Yaron, Y, Shomrat, R, Ben-Yehuda, A, Zabari, S, Peretz, H, Naiman, T, Yeger, H, Orr-Urtreger, A

“…The Fragile X syndrome is the most common cause of inherited mental retardation. For a female premutation carrier, the risk of having a child with a full…”
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Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi jews with familial colorectal neoplasia: evidence for a founder effect by ROZEN, Paul, NAIMAN, Tova, STRUL, Hana, TAUSSKY, Philipp, KARMINSKY, Nataly, SHOMRAT, Ruth, SAMUEL, Ziona, YARON, Yuval, ORR-URTREGER, Avi

“…The authors previously found the I1307K adenomatous polyposis coli (APC) gene variant in 5% of Ashkenazi control participants, in 15.4% of those who had…”
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O▪75 PGD for single gene disorders: the Tel-Aviv (Israel) Medical Centre Experience by Malcov, M, Naiman, T, Ben-Yosef, D, Frumkin, T, Schwarzt, T, Mey-Raz, B, Azem, F, Vagman, I, Amit, A, Yaron, Y

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Evaluating a Teacher Training Environmental Education Program in Papua New Guinea by Ormsby, A, Naiman, T, Berkovits, A

“…In order to support efforts to conserve the unique biodiversity of Papua New Guinea, the Wildlife Conservation Society initiated a teacher training…”
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Use of ASIF compression plates in selected shaft fractures of the upper extremity. A preliminary report by Naiman, P T, Schein, A J, Siffert, R S

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Medial displacement fixation for severely comminuted intertrochanteric fractures by Naiman, P T, Schein, A J, Siffert, R S

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Mapping of the human caseis kinase II catalytic subunit genes: two loci carrying the homologues sewquences for the α subunit by Yang-Feng, T. L, Zheng, K., Kopatz, I., Naiman, T., Canaani, D.

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Muir-Torre syndrome and HNPCC: importance of clinical diagnosis and genetic investigation in family members by Strul, H, Rozen, P, Naiman, T, Shomrat, R

“…Muir-Torre syndrome is a relatively rare cutaneous manifestation of hereditary nonpolypous colorectal cancer (HNPCC). This autosomal dominant syndrome is…”
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Assignment of the human casein kinase II alpha' subunit gene (CSNK2A1) to chromosome 16p13.2-p13.3 by Yang-Feng, T L, Naiman, T, Kopatz, I, Eli, D, Dafni, N, Canaani, D

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Establishment of an autocatalytic conditional mammalian system for expression of stringently regulated genes by Dotan, Iris, Kopatz, Idit, Naiman, Tova, Perelman, Boris, Dafni, Naomi, Canaani, Dan

“…Analysis of the biological roles and regulation of isolated genes in mammalian cells often requires inducible expression systems, particularly when the studied…”
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The nucleotide sequence of the mouse cDNA encoding the beta subunit of casein kinase II by Kopatz, I, Naiman, T, Eli, D, Canaani, D

“…We report the nucleotide sequence of a cDNA encoding the murine CK II-beta subunit. A lambda gt11 cDNA library prepared from the pre B mouse lymphoid cell line…”
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Mapping of the human casein kinase II catalytic subunit genes : two loci carrying the homologous sequences for the α subunit by YANG-FENG, T. L, ZHENG, K, KOPATZ, I, NAIRMAN, T, CANAANI, D

“…The human serine/threonine protein casein kinase II (CK II) contains two distinct catalytic subunits, alpha and alpha 1, which are encoded by different genes…”
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Isolation by polymerase chain reaction of a cDNA whose product partially complements the ultraviolet sensitivity of xeroderma pigmentosum group C cells by Teitz, T, Penner, M, Eli, D, Stark, M, Bakhanashvili, M, Naiman, T, Canaani, D

“…A xeroderma pigmentosum (XP) cell line from complementation group C has been complemented to attain ultraviolet (UV) resistance and DNA repair proficiency, by…”
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Immortalization of xeroderma pigmentosum cells by simian virus 40 DNA having a defective origin of DNA replication by CANAANI, D, NAIMAN, T, TEITZ, T, BERG, P

“…A simian virus 40 (SV40) DNA fragment, encompassing the whole early region and having a defective origin of DNA replication, has been used to transform human…”
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A hypodiploid karyotype found in immortal human cells selected from a wide spectrum of posttransformation chromosomal complements by Naiman, T, Canaani, D

“…A simian virus 40 (SV40) DNA fragment, encompassing the whole early region but having a defective origin of DNA replication, was previously used to transform…”
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Expression of the cDNA for the beta subunit of human casein kinase II confers partial UV resistance on xeroderma pigmentosum cells by Teitz, T, Eli, D, Penner, M, Bakhanashvili, M, Naiman, T, Timme, T L, Wood, C M, Moses, R E, Canaani, D

“…An immortalized xeroderma pigmentosum cell line belonging to the complementation group D (XP-D) was transfected with a normal human cDNA clone library…”
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