Bibliotecas PUC-SP - Busca Integrada

RFLP for C2/11 (D7S374), a cosmid for chromosome seven.

Por Scambler, P J, Lench, N J
Publicado em 1987

An anonymous DNA probe (NL32) recognises a MspI polymorphism on human chromosome 1 [D1S84].

Por Lench, N J, Scambler, P J
Publicado em 1988

Evidence for a common mutation in hereditary pancreatitis.

Por Bell, S M, Bennett, C, Markham, A F, Lench, N J
Publicado em 1998

Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primers.

Por Lench, N J, Norris, A, Bailey, A, Booth, A, Markham, A F
Publicado em 1996

AvaII RFLP detected by the anonymous DNA segment p10E5.SC1 [D11S806] on chromosome 11q22 – 23

Por Lench, N.J., Carpenter, S., Swift, M., Evans, G.A., McElligott, D.L.
Publicado em 1991

Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.

Por Brown, K A, al-Gazali, L I, Moynihan, L M, Lench, N J, Markham, A F, Mueller, R F
Publicado em 1997

A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24.

Por Mitchell, S J, McHale, D P, Campbell, D A, Lench, N J, Mueller, R F, Bundey, S E, Markham, A F
Publicado em 1998

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

Por McHale, D P, Mitchell, S, Bundey, S, Moynihan, L, Campbell, D A, Woods, C G, Lench, N J, Mueller, R F, Markham, A F
Publicado em 1999

Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.

Por Moynihan, L M, Bundey, S E, Heath, D, Jones, E L, McHale, D P, Mueller, R F, Markham, A F, Lench, N J
Publicado em 1998

Analysis of the IBD5 locus and potential gene-gene interactions in Crohn’s disease

Por Negoro, K, McGovern, D P B, Kinouchi, Y, Takahashi, S, Lench, N J, Shimosegawa, T, Carey, A, Cardon, L R, Jewell, D P, van Heel, D A
Publicado em 2003

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

Por Lench, N J, Markham, A F, Mueller, R F, Kelsell, D P, Smith, R J, Willems, P J, Schatteman, I, Capon, H, Van De Heyning, P J, Van Camp, G
Publicado em 1998

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

Por Jackson, A P, McHale, D P, Campbell, D A, Jafri, H, Rashid, Y, Mannan, J, Karbani, G, Corry, P, Levene, M I, Mueller, R F, Markham, A F, Lench, N J, Woods, C G
Publicado em 1998

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Por Campbell, D A, McHale, D P, Brown, K A, Moynihan, L M, Houseman, M, Karbani, G, Parry, G, Janjua, A H, Newton, V, al-Gazali, L, Markham, A F, Lench, N J, Mueller, R F
Publicado em 1997

The exon sequence TAGG can inhibit splicing.

Por Del Gatto, F, Gesnel, M C, Breathnach, R, Tsukamoto, Y, Kato, J, Ikeda, H, Brunar, H, Dervan, P B, Morrison, C, Wagner, E, Vigano, M A, Staudt, L M, Samarsky, D A, Schneider, G S, Fournier, M J, Yasugi, T, Howley, P M, Blake, R D, Delcourt, S G, Hasan, A, Li, H, Tomasz, J, Shaw, B R, Bielinska, A, Kukowska-Latallo, J F, Johnson, J, Tomalia, D A, Baker, J R, Wu, X, Li, J, Li, X, Hsieh, C L, Burgers, P M, Lieber, M R, Sandler, S J, Satin, L H, Samra, H S, Clark, A J, Glemarec, C, Kufel, J, Földesi, A, Maltseva, T, Sandström, A, Kirsebom, L A, Chattopadhyaya, J, Lench, N J, Norris, A, Bailey, A, Booth, A, Markham, A F, Li, J, Daniels, G A, Lieber, M R, Mathieu-Daudé, F, Welsh, J, Vogt, T, McClelland, M, Dagle, J M, Weeks, D L, Ellison, A R, Bishop, J O, Tabara, H, Motohashi, T, Kohara, Y, Moran, S, Ren, R X, Sheils, C J, Rumney, S, Kool, E T, Olmos, A, Dasí, M A, Candresse, T, Cambra, M, Belanger, K G, Mirzayan, C, Kreuzer, H E, Alberts, B M, Kreuzer, K N, Lukyanov, K A, Matz, M V, Bogdanova, E A, Gurskaya, N G, Lukyanov, S A, Farmer, A A, Johnsen, J I, Loftus, T M, Smith, K P, Stanbridge, E J, Bender, K, Federwisch, M, Loggen, U, Nehls, P, Rajewsky, M F, Petruska, J, Arnheim, N, Goodman, M F, Francès, V, Bastin, M, Abe, R, Yamamoto, K, Sakamoto, H, Todd, S, Semler, B L, Rahner, A, Schöler, A, Martens, E, Gollwitzer, B, Schüller, H J, McGuigan, A, Huxley, C, Liu, Z, Matthews, J R, Botting, C H, Panico, M, Morris, H R, Hay, R T, Harbers, M, Wahlström, G M, Vennström, B, Hamm, J, Ward, B, Boë, F, Masson, J M, Kuwabara, T, Amontov, S V, Warashina, M, Ohkawa, J, Taira, K, Wenzelides, S, Altmann, H, Wendler, W, Winnacker, E L, Chaturvedi, S, Horn, T, Letsinger, R L, Lebrun, A, Lavery, R, Ackermann, R, Brack, C, Zhang, H, Zhang, R, Liang, P, Schnetz, K, Wang, J C, Oechsner, U, Bandlow, W, Hug, A M, Feldmann, H, Hagiwara, K, Harris, C C, Sunters, A, Grimaldi, K A, Souhami, R L, Hartley, J A, Veronico, P, Gallerani, R, Ceci, L R, Alexander, H, Lee, S K, Yu, S L, Alexander, S
Publicado em 1996

A role for exon sequences in alternative splicing of the human fibronectin gene.

Por Mardon, H J, Sebastio, G, Baralle, F E, Hartmann, R K, Ulbrich, N, Erdmann, V A, Le Doan, T, Perrouault, L, Praseuth, D, Habhoub, N, Decout, J L, Thuong, N T, Lhomme, J, Hélène, C, Goding, C R, Temperley, S M, Fisher, F, Barthelemy, I, Lázaro, J M, Méndez, E, Mellado, R P, Salas, M, Koltunow, A M, Gregg, K, Rogers, G E, Montandon, P E, Knuchel-Aegerter, C, Stutz, E, Iverson, B L, Dervan, P B, Wiaderkiewicz, R, Ruiz-Carrillo, A, Wallenburg, J C, Nepveu, A, Chartrand, P, Vollrath, D, Davis, R W, Taljanidisz, J, Decker, R S, Guo, Z S, DePamphilis, M L, Sarkar, N, Edlind, T D, Chakraborty, P R, Benyajati, C, Ayer, S, McKeon, J, Ewel, A, Huang, J, Ronson, C W, Astwood, P M, Nixon, B T, Ausubel, F M, Corfield, P W, Hunter, W N, Brown, T, Robinson, P, Kennard, O, Purvis, I J, Bettany, A J, Loughlin, L, Brown, A J, Purvis, I J, Loughlin, L, Bettany, A J, Brown, A J, Plevani, P, Francesconi, S, Lucchini, G, Beri, R K, Whittington, H, Roberts, C F, Hawkins, A R, Cuniasse, P, Sowers, L C, Eritja, R, Kaplan, B, Goodman, M F, Cognet, J A, LeBret, M, Guschlbauer, W, Fazakerley, G V, Shields, D C, Sharp, P M, Distler, J, Ebert, A, Mansouri, K, Pissowotzki, K, Stockmann, M, Piepersberg, W, Miwa, K, Strominger, J L, McCarthy, J G, Heywood, S M, Drinkwater, R D, Wilson, P J, Skinner, J D, Burgoyne, L A, Gooding, C, Reinach, F C, Macleod, A R, Huber, M, Hütter, R, Lerch, K, Kikuchi, H, Sekiya, T, Nishimura, S, Watanabe, M, Knopf, C W, Vakulenko, S, Kálmán, M, Horváth, B, Simoncsits, A, Roth, S Y, Schulman, I G, Cook, R G, Allis, C D, Rose, E A, Munro, H N, Riggs, C D, Chrispeels, M J, Cornwell, T L, Adhya, S L, Reznikoff, W S, Frey, P A, Fukazawa, C, Momma, T, Higuchi, W, Udaka, K, Reymond, C D, Gatti, R A, Shaked, R, Wei, S, Mohandas, T K, Salser, W, Smeets, H, Markslag, P, Bril, J, Hulsebos, T, Brunner, H, Schonk, D, Ropers, H H, Wieringa, B, Scambler, P J, Lench, N J, Robbins, T P, Scambler, P J, Davies, K E, Williamson, R, Kozak, M, Musti, A M, Ursini, V M, Avvedimento, E V, Zimarino, V, Di Lauro, R, Anand, N N, Brown, D M, Salisbury, S A, Ernoult-Lange, M, Omilli, F, May, E, Lapoumeroulie, C, Acuto, S, Rouabhi, F, Labie, D, Krishnamoorthy, R, Bank, A, Rewinski, C, Marinus, M G, Sioud, M, Forterre, P, de Recondo, A M, Zacharias, M, Wagner, R
Publicado em 1987