Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.

Literature DB >> 14104609

DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.

E R HUEHNS, F HECHT, J V KEIL, A G MOTULSKY.

Abstract

Entities: Disease

Keywords: ADOLESCENCE; BLOOD PROTEIN ELECTROPHORESIS; CHILD; EXPERIMENTAL LAB STUDY; GENETICS, HUMAN; HEMOGLOBIN; HEMOGLOBINS, ABNORMAL; INFANT; INFANT, NEWBORN; TRISOMY

Mesh：

Substances：

Year: 1964 PMID： 14104609 PMCID： PMC300609 DOI： 10.1073/pnas.51.1.89

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

× No keyword cloud information.

20 in total

1. THE NO. 17-18 (E) TRISOMY SYNDROME. STUDIES ON CYTOGENETICS, DERMATOGLYPHICS, PATERNAL AGE, AND LINKAGE.

Authors: F HECHT; J S BRYANT; A G MOTULSKY; E R GIBLETT
Journal: J Pediatr Date: 1963-10 Impact factor: 4.406

2. GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME.

Authors: N J BRANDT; A FROLAND; M MIKKELSEN; A NIELSEN; N TOLSTRUP
Journal: Lancet Date: 1963-10-05 Impact factor: 79.321

3. A 'new' variant of haemoglobin A2 and its segregation in a family with haemoglobin S.

Authors: H M RANNEY; A S JACOBS; T B BRADLEY; F A CORDOVA
Journal: Nature Date: 1963-01-12 Impact factor: 49.962

4. Hemoglobin F1, an acetyl-containing hemoglobin.

Authors: W A SCHROEDER; J T CUA; G MATSUDA; W D FENNINGER
Journal: Biochim Biophys Acta Date: 1962-10-08

5. Dermal patterns of 18 and D1 trisomics.

Authors: I A UCHIDA; K PATAU; D W SMITH
Journal: Am J Hum Genet Date: 1962-12 Impact factor: 11.025

6. Four haemoglobins in one individual. A study of the genetic interaction of Hb-G and Hb-C.

Authors: A B RAPER; D B GAMMACK; E R HUEHNS; E M SHOOTER
Journal: Br Med J Date: 1960-10-29

7. Inhomogeneity of hemoglobin. VI. The minor hemoglobin components of cord blood.

Authors: B F HORTON; R B THOMPSON; A M DOZY; C M NECHTMAN; E NICHOLS; T H HUISMAN
Journal: Blood Date: 1962-09 Impact factor: 22.113

8. A new technique for differentiation of hemoglobin.

Authors: A R ROBINSON; M ROBSON; A P HARRISON; W W ZUELZER
Journal: J Lab Clin Med Date: 1957-11

9. [Demonstration of fetal hemoglobin in erythrocytes of a blood smear].

Authors: E KLEIHAUER; H BRAUN; K BETKE
Journal: Klin Wochenschr Date: 1957-06-15

10. Controller genes in synthesis of human haemoglobin.

Authors: A G MOTULSKY
Journal: Nature Date: 1962-05-12 Impact factor: 49.962

26 in total

1. [Neonatal polycythaemia and haemoglobin types in infants with G-trisomy (author's transl)].

Authors: E Kohne; E Kleihauer
Journal: Klin Wochenschr Date: 1975-02-01

2. QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.

Authors: E D WEINSTEIN; D L RUCKNAGEL; M W SHAW
Journal: Am J Hum Genet Date: 1965-09 Impact factor: 11.025

10. A human embryonic hemoglobin inhibits Hb S polymerization in vitro and restores a normal phenotype to mouse models of sickle cell disease.

Authors: Zhenning He; J Eric Russell
Journal: Proc Natl Acad Sci U S A Date: 2002-07-17 Impact factor: 11.205

DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.

1. THE NO. 17-18 (E) TRISOMY SYNDROME. STUDIES ON CYTOGENETICS, DERMATOGLYPHICS, PATERNAL AGE, AND LINKAGE.

2. GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME.

3. A 'new' variant of haemoglobin A2 and its segregation in a family with haemoglobin S.

4. Hemoglobin F1, an acetyl-containing hemoglobin.

5. Dermal patterns of 18 and D1 trisomics.

6. Four haemoglobins in one individual. A study of the genetic interaction of Hb-G and Hb-C.

7. Inhomogeneity of hemoglobin. VI. The minor hemoglobin components of cord blood.

8. A new technique for differentiation of hemoglobin.

9. [Demonstration of fetal hemoglobin in erythrocytes of a blood smear].

10. Controller genes in synthesis of human haemoglobin.

1. [Neonatal polycythaemia and haemoglobin types in infants with G-trisomy (author's transl)].

2. QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.

3. [EMBRYONIC HEMOGLOBINS].

4. A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21).

5. The switch from fetal to adult hemoglobin.

6. MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13.

7. Trisomy 13 with a 13-X translocation.

8. Genotype and phenotype in human chromosome aberrations and in the minute mutants of Drosophila melanogaster.

9. Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat.

10. A human embryonic hemoglobin inhibits Hb S polymerization in vitro and restores a normal phenotype to mouse models of sickle cell disease.