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1
Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta]
Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? [Carta]

Amanda G Silva Ana Cristina Victorino Krepischi; Giovana T Torrezan; Leonardo P Capelli; Dirce M Carraro; Carla S D'Angelo; Celia Priszkulnik Koiffmann; Mayana Zatz; Michel Naslavsky; Cibele Masotti; Paulo A Otto; Maria I. W Achatz; Ryan E Mills; Charles Lee; Peter L Pearson; Carla Rosenberg

European Journal of Human Genetics London online, p. 1-3 on-line, 2013

London 2013

Item não circula. Consulte sua biblioteca.(Acessar)

2
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity

Ali Jalali Kimberly A Aldinger; Ajit Chary; David G McLone; Robin M Bowman; Luan Cong Le; Phillip Jardine; Ruth Newbury-Ecob; Andrew Mallick; Nadereh Jafari; Eric J Russell; John Curran; Pam Nguyen; Karim Ouahchi; Charles Lee; William B Dobyns; Kathleen J Millen; João Monteiro Pina Neto; John A Kessler; Alexander G Bassuk

Human Genetics Heidelberg v. 123, n. 3, p. 237-245, 2008

Heidelberg 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1667232 )(Acessar)

3
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
Material Type:
Artigo 		Adicionar ao Meu Espaço

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity

Ali Jalali Kimberly A Aldinger; Ajit Chary; David G McLone; Robin M Bowman; Luan Cong Le; Phillip Jardine; Ruth Newbury-Ecob; Andrew Mallick; Nadereh Jafari; Eric J Russell; John Curran; Pam Nguyen; Karim Ouahchi; Charles Lee; William B Dobyns; Kathleen J Millen; João Monteiro Pina Neto; John A Kessler; Alexander G Bassuk

Human Genetics Heidelberg v. 123, n. 3, p. 237-245, 2008

Heidelberg 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1667232 )(Acessar)

4
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

David T. Miller Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John, A Crolla; E Eichler; Charles J Epstein; W. Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert H Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter

The American Journal of Human Genetics Cambridge v. 86 n. 5, p. 749-764, may 2010

Cambridge 2010

Item não circula. Consulte sua biblioteca.(Acessar)

5
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Consensus Statement chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

David T. Miller Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John, A Crolla; E Eichler; Charles J Epstein; W. Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert H Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter

The American Journal of Human Genetics Cambridge v. 86 n. 5, p. 749-764, may 2010

Cambridge 2010

Item não circula. Consulte sua biblioteca.(Acessar)

6
Proposal for a reaction mechanism to K49 phospholipases 'A IND.2'
Proposal for a reaction mechanism to K49 phospholipases 'A IND.2'
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Proposal for a reaction mechanism to K49 phospholipases 'A IND.2'

W. H. Lee Igor Polikarpov; Richard Charles Garratt; Reunião Anual de Usuários do Laboratório Nacional de Luz Síncrotron-LNLS (10. 2000 Campinas)

Resumos Campinas : LNLS, 2000

Campinas LNLS 2000

Item não circula. Consulte sua biblioteca.(Acessar)

7
Cigarette smoking and risk of prostate cancer in the physicians' health study (United States)
Cigarette smoking and risk of prostate cancer in the physicians' health study (United States)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cigarette smoking and risk of prostate cancer in the physicians' health study (United States)

Paulo Andrade Lotufo I-Min Lee; Umed A Ajani; Charles H Hennekens; JoAnn E Manson

International Journal of Cancer New York v. 87, p. 141-144, 2000

New York 2000

Acesso online. A biblioteca também possui exemplares impressos.

8
Structural basis for low catalytic activity in Lys49 phospholipases A2-A hypothesis the crystal structure of piratoxin II complexed to fatty acid
Structural basis for low catalytic activity in Lys49 phospholipases A2-A hypothesis the crystal structure of piratoxin II complexed to fatty acid
Material Type:
Artigo 		Adicionar ao Meu Espaço

Structural basis for low catalytic activity in Lys49 phospholipases A2-A hypothesis the crystal structure of piratoxin II complexed to fatty acid

Wen-Hwa Lee Maria Teresa da Silva Giotto; Sérgio Marangoni; Marcos H Toyama; Igor Polikarpov; Richard Charles Garratt

Biochemistry Washington v.40, p.28-36, 2001

Washington 2001

Localização: IFSC - Inst. Física de São Carlos    (PROD006985 )(Acessar)

9
Structural basis for low catalytic activity in Lys49 phospholipases A2-A hypothesis the crystal structure of piratoxin II complexed to fatty acid
Structural basis for low catalytic activity in Lys49 phospholipases A2-A hypothesis the crystal structure of piratoxin II complexed to fatty acid
Material Type:
Artigo 		Adicionar ao Meu Espaço

Structural basis for low catalytic activity in Lys49 phospholipases A2-A hypothesis the crystal structure of piratoxin II complexed to fatty acid

Wen-Hwa Lee Maria Teresa da Silva Giotto; Sérgio Marangoni; Marcos H Toyama; Igor Polikarpov; Richard Charles Garratt

Biochemistry Washington v.40, p.28-36, 2001

Washington 2001

Localização: IFSC - Inst. Física de São Carlos    (PROD006985 )(Acessar)

10
Physical activity during adolescence and risk of colorectal adenoma later in life results from the Nurses' Health Study II
Physical activity during adolescence and risk of colorectal adenoma later in life results from the Nurses' Health Study II
Material Type:
Artigo 		Adicionar ao Meu Espaço

Physical activity during adolescence and risk of colorectal adenoma later in life results from the Nurses' Health Study II

Leandro Fornias Machado de Rezende Dong Hoon Lee; NaNa Keum; Katharina Nimptsch; Mingyang Song; I-Min Lee; José Eluf Neto; Shuji Ogino; Charles Fuchs; Jeffrey Meyerhardt

British journal of cancer v. 121, n. 1, p. 86-94, 2019

London 2019

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Lee, E
  2. Lee, C
  3. Oliveira, R
  4. Garratt, R
  5. Dias, L

Neste Assunto:

  1. Biologia Molecular
  2. Bioquímica
  3. Proteínas
  4. Genética Médica
  5. Neurologia

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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